Current Chemistry Job Vacancies - Worldwide

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Postgraduate Research Associate: Employment of Volatile Organic Compounds

The Department of Agrobiotechnology (IFA-Tulln), Center for Analytical Chemistry, Metabolomics group in Vienna, Austria, is currently seeking a Postgraduate Research Associate (project employment): Employment of Volatile Organic Compounds (VOCs) produced by Lysobacter for biocontrol of soilborne plant pathogens [applications can be submitted until: 31th of March 2017].



Professorship (W3) of Product Design

Staatliche Hochschule für Gestaltung (HFG) Karlsruhe
Datum: 24.05.2017


Professorship (W3) Social services in structurally weak areas

Brandenburg University of Technology (BTU) Cottbus-Senftenberg
Datum: 24.05.2017


Independent Research Group Leader (f/m) in the Cyber Valley Initiative

Max Planck Institute for Intelligent Systems / University of Stuttgart / University of Tübingen
Datum: 24.05.2017


Junior researchers with expertise in life sciences or bioinformatics/informatics

University of Freiburg / Max Planck Institute of Immunobiology and Epigenetics Freiburg
Datum: 24.05.2017


Full Professorship (W3) of Physiology

University of Hohenheim
Datum: 23.05.2017


Associate Senior Lecturer in Molecular Plant-Pest/Disease Interactions

Swedish University of Agricultural Sciences (SLU)
Datum: 22.05.2017


Fellowships in the Humanities "Law as Culture"

Käte Hamburger Kolleg "Recht als Kultur"
Datum: 22.05.2017


Software Developer (f/m) in the DEEP-EST Project

Forschungszentrum Jülich GmbH
Datum: 22.05.2017


PhD positions Data Science and Systems Complexity COFUND Programme

University of Groningen
Datum: 22.05.2017


Research assistant at the School for Economics and Management (f/m)

Technische Universität Berlin
Datum: 22.05.2017


Early Career Research Group Leader (f/m)

Eberhard Karls Universität Tübingen
Datum: 19.05.2017


Professorship (W2) Biotechnology

Technical University of Munich (TUM)
Datum: 19.05.2017


Professorship (W2) in Management and Economics with a focus on Bioeconomy

Technical University of Munich (TUM)
Datum: 19.05.2017


Chair (W3) "CSC - Carbon Sources and Conversion"

Ruhr-Universität Bochum / Fraunhofer Institute for Environmental, Safety, and Energy Technology / RWE Power AG
Datum: 18.05.2017


Professor / Associate Professor / Lecturer (f/m) in Human Resources & Organizational Behavior

German University in Cairo (GUC)
Datum: 18.05.2017


Professorship in Sociology (W2, tenure track) with a special focus on Women's and Gender Research

Goethe University Frankfurt/Main
Datum: 18.05.2017


Professorship (W3) in Precision Engineering

University of Stuttgart
Datum: 18.05.2017


Professur (W2) Beverage Technology

Hochschule Ostwestfalen-Lippe
Datum: 18.05.2017


Professorship (W2) in "Geotechnics and the Principles of Civil Engineering"

Magdeburg-Stendal University of Applied Sciences
Datum: 17.05.2017


Tenure Track or Tenured Professor of Sustainability in Business

Aalto University School of Business
Datum: 17.05.2017


Professorship (W2) in Economics and International Economic Relations

Hochschule Konstanz Technik, Wirtschaft und Gestaltung (HTWG)
Datum: 17.05.2017


Assistant/Associate Professor (f/m) in Marketing

Tilburg University
Datum: 17.05.2017


PhD - "Game based learning: assessment and instructional interventions"

Universiteit Twente
Datum: 17.05.2017


CDM - Postdoc / Scientific Assistant position (f/m) in Green Economy

École polytechnique fédérale de Lausanne (EPFL)
Datum: 17.05.2017


Wissenschaftlicher Mitarbeiter (m/w) Produktionsinformatik

Fraunhofer-Institut für Optronik, Systemtechnik und Bildauswertung (IOSB)
Datum: 16.05.2017


Professorship of Building Product Innovation

Delft University of Technology
Datum: 16.05.2017


Assistant professorship in ICT, data and civil engineering specialised in experimental fluid & sediment dynamics

University of Twente
Datum: 16.05.2017


Project Researcher / Postdoc on the subject of Blockchains, Dynamic Contracts and Autonomous Negotiation for Smart Grids (f/m)

Centrum Wiskunde en Informatica (CWI)
Datum: 16.05.2017


Bioinformatiker / Informatiker (m/w)

Universität Hohenheim
Datum: 15.05.2017


Professorship (W3) in Special needs and inclusive education and pedagogy for physical impairments and chronical diseases

Martin- Luther-University of Halle-Wittenberg
Datum: 15.05.2017


University Professorship (W3) for the chair of "Control Engineering"

Technische Universität Berlin
Datum: 15.05.2017


PhD Studentship in Demography / Population Studies

Max-Planck-Institut für demografische Forschung (MPIDR)
Datum: 15.05.2017


Professorship (W2) in Education for support needs in learning

Martin- Luther-University of Halle-Wittenberg
Datum: 15.05.2017


Professorship (W2) in Education of emotionally and behaviorally disordered children

Martin- Luther-University of Halle-Wittenberg
Datum: 15.05.2017


W2-Professorship "Marketing, focusing on Fashion Retail" at Münster School of Business

Fachhochschule Münster
Datum: 12.05.2017


Doctoral Fellowships

Ageras
Datum: 12.05.2017


Professorship in Business Administration

BAU International Berlin - University of Applied Sciences
Datum: 11.05.2017


Full Professorship (W3) of Economics with a specialization in quantitative economic history

University of Bayreuth
Datum: 11.05.2017


PostDoc (m/f) at the department Molecular Epidemiology

German Institute of Human Nutrition Potsdam-Rehbruecke
Datum: 11.05.2017


PostDoc (m/f) at the department Molecular Epidemiology

German Institute of Human Nutrition Potsdam-Rehbruecke
Datum: 11.05.2017


Full Professorship (W3) of Economic Geography

University of Bayreuth
Datum: 11.05.2017


Professorship (W2) of Technical and Business English

Technische Hochschule Nürnberg Georg Simon Ohm
Datum: 11.05.2017


Research Associate (f/m) in the Field of Audio and Media Technologies

Fraunhofer Institute for Integrated Circuits IIS
Datum: 09.05.2017


Full Professorship for Entrepreneurship and Innovation

Universität St. Gallen
Datum: 08.05.2017


Assistant Professor Information Systems and Supply Chain Analytics (f/m)

Universiteit Twente
Datum: 05.05.2017


Assistant Professorship Reliability, Maintenance and Service

Universiteit Twente
Datum: 05.05.2017


PhD student (f/m) Neuroscience, Bioinformatics, Biotechnology, Biomedical Engineering, Computer Science

Deutsches Zentrum für Neurodegenerative Erkrankungen e.V. (DZNE)
Datum: 04.05.2017


Professur (W2) for Anaesthesia and Critical Care Medicine

Goethe-Universität Frankfurt am Main
Datum: 04.05.2017


Postdoctoral Researcher (f/m) in the area of Management Accounting and Control

WHU - Otto Beisheim School of Management
Datum: 03.05.2017


Research Assistant / Doctoral Student (f/m)

WHU - Otto Beisheim School of Management
Datum: 03.05.2017


Assistant Professorship in the area of Management Accounting and Control

WHU - Otto Beisheim School of Management
Datum: 03.05.2017


Professorship in Computer Architectures for embedded Systems

University of Twente (UT)
Datum: 03.05.2017


Associate Professorship (W2) in Virology

Charité - Universitätsmedizin Berlin
Datum: 02.05.2017


Full Professorship (W3) in "Tumor Biology"

Technische Universität München (TUM)
Datum: 02.05.2017


Universitätsprofessur (W3) für Mittelalterliche Geschichte mit dem Schwerpunkt Hoch- und Spätmittelalter

Freie Universität Berlin
Datum: 02.05.2017


Professorship / Associate Professorship / Lecturer Visual Design and Presentation (f/m)

German University in Cairo (GUC)
Datum: 02.05.2017


Full professorship in Computer Architectures for Embedded Systems (CAES)

Universiteit Twente
Datum: 02.05.2017


Full Professorship (W3) of Livestock Systems Engineering

Universität Hohenheim
Datum: 01.05.2017


Postdoc fellowship in Analytical Sciences

School of Analytical Sciences Adlershof (SALSA)
Datum: 28.04.2017


W2-Professorship for Epidemiology

Rheinische Friedrich-Wilhelms-University of Bonn
Datum: 27.04.2017


Full Professorship of Operations Management

Vienna University of Economics and Business
Datum: 27.04.2017


Professorship (W3) in "Analysis and Modelling"

Technical University of Munich (TUM)
Datum: 27.04.2017


Lecturer-Instructor - Product Design (f/m)

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship/Associate Professorship/Lecturer (f/m) Building Construction and Design

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship / Associate Professorship / Lecturer (f/m) in Analytical Chemistry

German University in Cairo (GUC)
Datum: 24.04.2017


Associate Professorship in Economics

German University in Cairo (GUC)
Datum: 24.04.2017


Instructor (f/m) Film/Video

German University in Cairo (GUC)
Datum: 24.04.2017


Lecturer (f/m) Typography/Font Design/Layout

German University in Cairo (GUC)
Datum: 24.04.2017


Instructor (f/m) Drawing

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship / Lecturer (f/m) in Operations and Production Management

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship / Associate Professor / Lecturer Architectural Design - Focus Housing

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship / Associate Professorship in Strategic Management

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship in International Business

German University in Cairo (GUC)
Datum: 24.04.2017


Lecturer/Instructor (f/m) Interaction Design

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship / Associate Professorship / Lecturer (f/m) Technical Systems and Building Physics

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship / Associate Professorship / Lecturer Architectural Theory and Design

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship of Physics

German University in Cairo (GUC)
Datum: 24.04.2017


Lecturer/Instructor (f/m) Photography

German University in Cairo (GUC)
Datum: 24.04.2017


Lecturer/Instructor (f/m) Digital Compositing

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship in Finance

German University in Cairo (GUC)
Datum: 24.04.2017


Lecturer in Mathematics (f/m)

German University in Cairo (GUC)
Datum: 24.04.2017


Professorship / Associate Professorship in Pharmaceutical Biology (Pharmacognosy)

German University in Cairo (GUC)
Datum: 24.04.2017


Chair in Social Anthropology

University of Amsterdam (UvA)
Datum: 19.04.2017


PhD / Postdoc position - Psychology, Literary Studies, Linguistics, Computational Linguistics or Neuroscience

Max-Planck-Institut für empirische Ästhetik (MPIEA)
Datum: 19.04.2017


Junior Research Groups at JMU "Excellent Ideas"

Julius-Maximilians-Universität Würzburg
Datum: 19.04.2017


Sunflower Breeder (f/m)

KWS Services Deutschland GmbH
Datum: 13.04.2017


Assistant Professorship (f/m) in ecotoxicogenomics

Stockholm University
Datum: 12.04.2017


Associate Professorship (f/m) in environmental chemistry specializing in non-polar contaminants

Stockholm University
Datum: 12.04.2017


Professorship (f/m) in organic analytical chemistry with environmental science applications

Stockholm University
Datum: 12.04.2017


Juniorprofessur (W1) mit Tenure Track Option, FG Kunstwissenschaft und Ästhetische Theorie

Universität Bremen
Datum: 12.04.2017


Full Professorship (W3) in Political Theory and History of Political Idea

RWTH Aachen University
Datum: 12.04.2017


Research Group Leader (f/m)

Leibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK)
Datum: 05.04.2017


Leiter (m/w) der Kompetenzgruppe Immobilienmanagement

Zürcher Hochschule für Angewandte Wissenschaften (ZHAW) Winterthur
Datum: 05.04.2017


Junior Group Leader (f/m) Symposium

Philipps-Universität Marburg
Datum: 04.04.2017


Professur (W2/W3) für Theoretische Philosophie

Universität Bremen
Datum: 22.03.2017


Professor (f/m) of Entrepreneurship and Technological Transformation

Otto Beisheim School of Management (WHU Vallendar)
Datum: 21.03.2017


Faculty Positions (f/m) in Robotics and Mechatronics

Nazarbayev University
Datum: 03.02.2017


Assistant/Associate Professorship in Applied Mathematics and Statistics

Nazarbayev University
Datum: 03.02.2017


Department Chair (f/m) Chemistry

Nazarbayev University
Datum: 03.02.2017


Associate Professorship Computer Science

Nazarbayev University
Datum: 03.02.2017


Department Chair (f/m) Computer Science

Nazarbayev University
Datum: 03.02.2017


Assistant Professorship in Biomedical Sciences

Nazarbayev University
Datum: 03.02.2017


Faculty Positions (f/m) in Chemistry

Nazarbayev University
Datum: 03.02.2017


Department Chair (f/m) Biology

Nazarbayev University
Datum: 03.02.2017


Research Technician / Laboratory Officer in Charge - Centre for Structural Systems Biology

Job Description The European Molecular Biology Laboratory (EMBL) is one of the highest ranked scientific research organisations in the world. The Headquarters Laboratory is located in Heidelberg (Germany), with additional sites in Grenoble (France), Hamburg (Germany), Hinxton (UK) and Monterotondo (Italy). We are looking for a research technician to set up and manage an experimental laboratory and perform research in the newly established group of Jan Kosinski at EMBL Hamburg and the Centr...
Datum: 26.05.2017


Postdoctoral Fellow - Discovery Chemistry

Novartis, San Diego, CA, USA - May 25th
Datum: 25.05.2017


Chemist / Senior Chemist Job (Singapore, SG)

Chemist / Senior Chemist-QUA004683

Description

- Responsible for planning, scheduling and performing laboratory testing of raw materials, packaging components, excipients, in-process control samples, intermediates, semi-finished products, final drug substances and finished products manufactured in API West, Biotech, Pharm West and Pharm South Facilities.
- Responsible for ensuring the analytical methods / specifications used are in accordance with requirements specified in MSD Quality Standards, regulatory dossiers and pharmacopoeia.
- Manage the calibration, maintenance and qualification of laboratory equipment.
- Conduct laboratory investigation on laboratory equipment failure, OOT and OOS.
- Responsible for testing of developmental and clinical products as required.
- Participate in analytical developmental activities as required.

CHEMIST:
- Perform analytical testing on incoming raw materials, packaging components and excipients.
- Carry out testing activities associated with release and stability testing of the in-process control samples, intermediates, semi-finished products, final drug substances & finished products.
- Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures with necessary laboratory safety precautions.
- Carry out cleaning sample testing related to any equipment or facility cleaning activities.
- Co-ordinate with respective IPT facilities on the timing of drug substances change-over.
- Perform second person verification of other analysts’ work.
- Liaise and coordinate with external service providers in carrying out calibration/maintenance of lab equipment and tools when necessary.
- Carry out lab equipment calibration and proper documentation of all instruments in laboratories.
- Closely work with supervisor on the requirements of swabbing samples and to identify the appropriate sampling location and take swab samples for testing.
- Participate in analytical method transfer / validation and equipment Qualifications when necessary.
- Perform periodic reviews of existing cleaning method validation package & procedure, and to implement corrective actions for the periodic reviews.
- Assist in writing protocol to support method transfer/validation, compendial method verification and equipment qualifications when necessary.
- Conduct in Laboratory investigation using 5 whys & fishbone to identify the root cause and its report writing. Ensure laboratory related actions are effectively implemented within agreed time frame, to continually improve processes, prevent waste, and eliminate rework.
- Provides inputs to new Quality Standards and Standard Analytical Tests; implementing new Quality Standards once approved and obsoleting previous revisions
- • Revise and write Standard Operating Procedures (SOPs) to reflect the current practice and ensuring that the current level of standard are met.
- Oversee Annual Product Review to ensure that the activities are completed by the required timelines
- Perform and maintain an acceptable level of good laboratory housekeeping.
- Maintain inventory and control in-house stock, reference standards, chemical reagents, and consumables and ensure that there are sufficient stocks for testing.
- Identify and execute laboratory efficiency improvement tasks, e.g., Kaizen.
- Any other duties as assigned by the Supervisor / Manager.

SENIOR CHEMIST:

In addition to the responsibilities of CHEMIST:

- Facilitate training of new recruits and generate the necessary training records and Analyst Qualification and Re-qualification Form (AQRF) for the trainee.
- Revise and write Standard Operating Procedures (SOPs) to reflect the current practice and ensuring that the current level of standard are met.
- Assist in responding to queries raised by regulatory agencies pertaining to analytical standards and methods.
- Assist in periodic review of laboratory procedures and ensure that current practices and standards are incorporated and reflected in the procedures.
- Responsible for release of batch results
- Supports Laboratory related metrics analysis and reporting
- Ensure all staff are appropriately trained and qualified to execute the duties assigned to them with respect to job, cGMP, GLP and SHE expectations as defined in the training matrix
- Schedule periodic review of test procedure to ensure the test methods and specifications are in line with current requirement specified in MSD Quality Standards, regulatory dossiers and pharmacopoeia.
- Work closely with global compendial group in reviewing of compendial changes and revise site test procedure and specification if necessary.
- Review of all the tests datasheet / worksheet records to ensure that the testing results are within SPC limits and meet Product Specification.
- Participate in SHE, Business Compliance, cGMP and all other compliance-related matters, where applicable.

Qualifications

- Bachelor Degree in Chemistry/ Biochemistry.
- Prior working experience is preferred.

CHEMIST:

- 0 – 3 years experience in pharmaceutical analysis is preferred.
- Experience in operating laboratory equipment such as Particle size analyzer, GC, HPLC, Karl Fischer Titrator is preferred.

SENIOR CHEMIST:

- 4 – 6 years experience in pharmaceutical analysis is preferred.
- Demonstrable experience and competency in Particle size analyzer, GC, HPLC, Karl Fischer Titrator, spectroscopic and wet chemistry testing is preferred.
- Demonstrated knowledge and application of sound scientific principles, theories, techniques and skills.
- Technical competency in analytical troubleshooting.
- Demonstrated knowledge and understanding of cGMP, GLP, and associated regulatory expectations related to Pharmaceutical Analytical Testing and Release
- Potential to teach and coach the team on technical and business process elements of analytical testing.

Job: Quality Lab Related Job Title:Chemist / Senior Chemist

Primary Location: APAC-SG-Singapore-Singapore

Employee Status: Regular

Travel: No

Company Trade Name:MSD
Datum: 25.05.2017


IT Project & Support Engineer Job (Haarlem, NL)

IT Project & Support Engineer-SER001064

Description

Position Overview

The IT Project and Support Engineer is responsible for supporting the operation, planning and execution of the IT projects related to infrastructure. He/she assures compliance with the applicable global and country regulatory requirements as well as global policies and standards pertaining to IT infrastructure.

Through effective communications with local and global stakeholders, a translation of business needs will be conveyed to allow for a right sized infrastructure. The IT infrastructure comprises laptop/desktop, networks, security, servers, printing and telephony throughout all business divisions within the market and on the site. A close cooperation with IT colleagues as well as the business will be required to deliver IT infrastructure capable to support the business needs.

He/she will be responsible for supporting the IT infrastructure and, in close cooperation with the GIO (Global Infrastructure Operations) site lead, run or participate in IT infrastructure related projects. The IT Project and Support Engineer will be part of the global MSD ‘One IT’ team based in the Netherlands with key service focus towards the MSD site where he/she is based.

Responsibilities & Activities

“One IT” – Overall responsibilities:

- Champions the One IT Operating Model
- Ensures and promote collaboration with other IT divisions as well as parts of the MSD business, both locally and globally, to break-down organizational boundaries in favor of a highly-collaborative and customer-centric culture
- Drives continuous improvement and innovation, develops and outside-in view based on cross-industry networking
- Assures, and is able to demonstrate full compliance of functional area IT systems and processes, and this towards both company requirement as well as applicable regulatory requirements.

IT Infrastructure Service Management:

- Operates and implements all IT infrastructures in scope, including appropriate application of globally defined processes around Configuration Management, Change Management, and Incident/Problem Management.
- Implements a sustainable service model for all infrastructures deployed, consisting of end user IT devices as well as back-office infrastructure locally implemented.
- Corporate with external service providers to ensure service levels are met. Provide service level reports and KPI's.
- Ensure that IT services and solutions meet GxP and SOX compliance. Provide required documentation and reporting. Manage corrective and preventive actions
- Partners with all IT colleagues in the Netherlands to align technology, processes and support within the Netherlands.
- Implementation and execution of Infrastructure Services projects. Projects are driven by business programs or are based on new demand coming from the implementation of TS global programs and standards. Participate in divisional IT projects for the implementation of TS Infrastructure. Monitor and report progress.
- Proactively ensure the implementation of MSD's IT infrastructure standards. This includes IT infrastructure standards, processes and standard service solutions. Ensure support of the legacy IT landscape until decommissioning. Onboarding of additional services in line with the global managed services strategy

Qualifications

Education & Experience Level:

- Education: MSc Degree or BSc Degree or equivalent with relevant experience in Computer Science, Computer Science Engineering, Math, or equivalent experience
- Minimum 3 years relevant experience
- Proven experience of working within an IT service framework (ITIL), throughout the service lifecycle
Overall Leadership Behaviors:

- Demonstrate ethics and integrity
- Drive results
- Focus on Customers and patients
- Make rapid disciplined decisions
- Act with courage and candor
- Build talent
- Foster collaboration
Overall Professional Competencies

- Working across boundaries
- Strategic thinking
- Business & Financial acumen
- Project Management
- Excellen communication skills in English and Dutch
- Problem Solving
About MSD
MSD is working to help the world be well. Through our medicines, vaccines, biologic therapies and animal health products, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. MSD has a workforce of almost 4500 in the Netherlands at three main sites.

MSD. Be well. For more information, visit our website: msd.nl/career/

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

A good place to work
MSD is an attractive employer offering interesting opportunities in Research & Development, production and staff departments for an enormous range of disciplines such as biologists, chemists, process engineers, technicians, mechatronic engineers, pharmacists and operators. MSD always seeks ‘best-in-class’ employees at all levels. We expect a lot from our people and MSD has a lot to offer them as well. Team spirit, entrepreneurship, integrity, leadership and cross-border communication skills are what MSD values and rewards most. If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Information:
For further information regarding this position, please contact Edwin Lek, Associate Director Global Infrastructure Operations, phone +31 412 663 383.

Application
If you are interested in this challenging role, you are requested to apply online by uploading your resume and application letter in English.

Job: Service Delivery/Management Job Title:Spclst, Service Delivery/Management

Primary Location: EMEA-Netherlands-NH-Haarlem

Employee Status: Regular

Travel: Yes, 5 % of the Time

Number of Openings: 1

Company Trade Name:MSD
Datum: 25.05.2017


IT Project & Support Engineer Job (Oss, NL)

IT Project & Support Engineer-SER001075

Description

Position Overview

The IT Project and Support Engineer is responsible for supporting the operation, planning and execution of the IT projects related to infrastructure. He/she assures compliance with the applicable global and country regulatory requirements as well as global policies and standards pertaining to IT infrastructure.

Through effective communications with local and global stakeholders, a translation of business needs will be conveyed to allow for a right sized infrastructure. The IT infrastructure comprises laptop/desktop, networks, security, servers, printing and telephony throughout all business divisions within the market and on the site. A close cooperation with IT colleagues as well as the business will be required to deliver IT infrastructure capable to support the business needs.

He/she will be responsible for supporting the IT infrastructure and, in close cooperation with the GIO (Global Infrastructure Operations) site lead, run or participate in IT infrastructure related projects. The IT Project and Support Engineer will be part of the global MSD ‘One IT’ team based in the Netherlands with key service focus towards the MSD site where he/she is based.

Responsibilities & Activities

“One IT” – Overall responsibilities:

- Champions the One IT Operating Model
- Ensures and promote collaboration with other IT divisions as well as parts of the MSD business, both locally and globally, to break-down organizational boundaries in favor of a highly-collaborative and customer-centric culture
- Drives continuous improvement and innovation, develops and outside-in view based on cross-industry networking
- Assures, and is able to demonstrate full compliance of functional area IT systems and processes, and this towards both company requirement as well as applicable regulatory requirements.

IT Infrastructure Service Management:

- Operates and implements all IT infrastructures in scope, including appropriate application of globally defined processes around Configuration Management, Change Management, and Incident/Problem Management.
- Implements a sustainable service model for all infrastructures deployed, consisting of end user IT devices as well as back-office infrastructure locally implemented.
- Corporate with external service providers to ensure service levels are met. Provide service level reports and KPI's.
- Ensure that IT services and solutions meet GxP and SOX compliance. Provide required documentation and reporting. Manage corrective and preventive actions
- Partners with all IT colleagues in the Netherlands to align technology, processes and support within the Netherlands.
- Implementation and execution of Infrastructure Services projects. Projects are driven by business programs or are based on new demand coming from the implementation of TS global programs and standards. Participate in divisional IT projects for the implementation of TS Infrastructure. Monitor and report progress.
- Proactively ensure the implementation of MSD's IT infrastructure standards. This includes IT infrastructure standards, processes and standard service solutions. Ensure support of the legacy IT landscape until decommissioning. Onboarding of additional services in line with the global managed services strategy

Qualifications

Education & Experience Level:

- Education: MSc Degree or BSc Degree or equivalent with relevant experience in Computer Science, Computer Science Engineering, Math, or equivalent experience
- Minimum 3 years relevant experience
- Proven experience of working within an IT service framework (ITIL), throughout the service lifecycle
Overall Leadership Behaviors:

- Demonstrate ethics and integrity
- Drive results
- Focus on Customers and patients
- Make rapid disciplined decisions
- Act with courage and candor
- Build talent
- Foster collaboration
Overall Professional Competencies

- Working across boundaries
- Strategic thinking
- Business & Financial acumen
- Project Management
- Excellent communication skills in both English and Dutch
- Problem Solving
About MSD
MSD is working to help the world be well. Through our medicines, vaccines, biologic therapies and animal health products, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. MSD has a workforce of almost 4500 in the Netherlands at three main sites.

MSD. Be well. For more information, visit our website: msd.nl/career/

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

A good place to work
MSD is an attractive employer offering interesting opportunities in Research & Development, production and staff departments for an enormous range of disciplines such as biologists, chemists, process engineers, technicians, mechatronic engineers, pharmacists and operators. MSD always seeks ‘best-in-class’ employees at all levels. We expect a lot from our people and MSD has a lot to offer them as well. Team spirit, entrepreneurship, integrity, leadership and cross-border communication skills are what MSD values and rewards most. If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Information:
For further information regarding this position, please contact Edwin Lek, Associate Director Global Infrastructure Operations, phone +31 412 663 383.

Application
If you are interested in this challenging role, you are requested to apply online by uploading your resume and application letter in English.

Job: Service Delivery/Management Job Title:Spclst, Service Delivery/Management

Primary Location: EMEA-Netherlands-NB-Oss

Employee Status: Regular

Travel: Yes, 5 % of the Time

Number of Openings: 1

Company Trade Name:MSD
Datum: 25.05.2017


Lead Engineer, Global Technical Operations Job (Singapore, SG)

Lead Engineer, Global Technical Operations-CHE004717

Description

The GTO Lead introduces new products to the site, providing technical expertise on the manufacture of all drug products on site and transferring drug products to other facilities. In collaboration with supporting functional groups, the GTO Lead provides technical guidance on deviations, investigations and customer complaints. The GTO Lead leads continuous process improvement activities to enhance site performance metrics and contributes to global technical networks to share site experiences and expand on personal and site expertise.

- Leads new product introductions to the site by assisting with process and equipment comparisons, new raw material introduction, development studies, cleaning processes development and validation, process fit and gap analysis.
- Supports filing activities by leading process qualification activities, equipment qualification and cleaning validation. Expected to have the expertise knowledge of QMS chapter 13, 17 and 25 and 35 (sterile) and understands the principles of Quality by Design (QbD) and executes the requirements in support of a QbD filing
- Supports routine supply manufacture by providing on going technical support to the IPT and proactively monitoring the performance of equipment/module(s) or unit operation(s) during manufacturing and cleaning. Responds to shifts and trends in performance appropriately and based on the data identifies opportunities for improvement.
- The GTO Lead is the change owner for process Global Change Management (GCM) change controls.
- Leads and mentors in developing continuous process verification (CPV) plans and contributes and reviews to the CPV reports and annual product reviews. Conversant and able to coach in statistical analysis.
- Provides and coaches/mentors the GTO Engineers/Chemists in technical expertise related to equipment and manufacturing/cleaning processes in response to deviations and atypical events to understand and eliminate the root cause(s).
- Leads investigations for non-emergency product complaints and deviations using problem solving tools such as KT. Ishikawa, FMEA, 5 Whys. Coaches the GTO Engineer/Chemist in problem solving skills.
- Leads collaboration and sharing of best practices with internal/external SMEs (e.g. CPDC, PCT, Sterile council, ADC, CMSE and other groups within the GSTC network.
- Complies with all divisional and site-specific policies, guidelines and procedures. Making safety adherence as a pre-requisite to employment.
- Demonstrates and promotes safety, health & environment (SHE) leadership behaviour, ensuring that all activities are carried out in accordance with SHE requirements. Actively participates in GEMBA safety walk, HazOp. Speak on process safety and lead by example GTO safety commitments.
- Where applicable, develops and reviews SOPs, gap analysis and Job Aids for GTO Subsystems in compliance with divisional and corporate policies and guidelines
- Demonstrate leadership behavior in alignment with MSD leadership standards (Individual Contributor)
- Practice Inclusion as the How and MSD Production Systems (MPS)
- Leads personal career development with manager assistance through annual Performance Management Process (PMP), Employee Development Plan (EDP) and career mapping.
- Any other duties as assigned by the Supervisor.

Qualifications

*
Bachelors,
Masters or Ph.D. degree in a technical field, including Chemical or Mechanical
Engineering, Chemistry or Pharmaceutical Sciences

*
Minimum
4 years technical experience in pharmaceutical manufacturing industry

*
Expert knowledge of core
technology/unit operations relevant to active pharmaceutical ingredient,
Biotech and/or Non-Sterile manufacturing

Job: Chemical Engineering Job Title:Engineer / Senior Engineer, Global Technical Operations

Primary Location: APAC-SG-Singapore-Singapore

Employee Status: Regular

Travel: No

Company Trade Name:MSD
Datum: 25.05.2017


Associate Principal Scientist - Residue Chemist Job (Madison, NJ, US)

Associate Principal Scientist - Residue Chemist-PHA001379

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its 125-year legacy. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Merck’s Animal Health (MAH) division works to improve the health of animals around the world through collaborative partnerships and a deep sense of responsibility towards our customers, consumers, animals, society, and our planet. This team of energetic, independent thinkers offers one of the industry’s most innovative portfolios of products, services, and technologies that serve to prevent, treat, and control diseases across all major farm and companion animal species both domestically and internationally.

The candidate should be knowledgeable in the conduct of residue, metabolism and bioanalytical studies to support veterinary drug development in food producing animals. Specific roles and tasks include, but are not limited to, study director, study monitor, study design, the preparation and the review of study protocols, study data, final reports, and responses to questions from regualtory agencies.

Qualifications

Education Minimum Requirement:

- Ph.D with at least two years of experience in analytical chemistry, biochemistry, or a closely-related discipline

Required Experience and Skills:

- Knowledge of US-FDA and EU-CVMP guidelines on veterinary drug development for food producing animals

- Knowledge in conducting residue chemistry, metabolism and bioanalytical studies to support domestic and international registration of pharmaceuticals in food producing animals

- Familiarity with guidelines that govern the use of animals to conduct residue studies

- Experience with quantitative and/or qualitative chromatographic techniques, in particular LC-MS/MS, HPLC-UV/VIS/FL and computerized automation of laboratory equipment as it pertains to residue chemistry and bioanalytical studies

- Knowledge of Good Laboratory Practice (GLP) regulations and regulations on electronic records

- Proficient in written communications and in the preparation of study documents for submission to regulatory agencies

- Excellent verbal communication and presentation skills required; team player required to represent the group in internal meetings, in meetings with regulatory officials and in scientific meetings

- Working knowledge of standard computer software applications for general office work use and for laboratory equipment

- Domestic travel required

Preferred Experience and Skills:

- Experience with US-FDA and EU-CVMP guidelines for conducting metabolism and residue chemistry studies for veterinary pharmaceuticals in food producing animals

- Experience with conducting and supervising method validation, residue depletion and pharmacokinetics studies to support drug development for food producing animals

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement?



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Pharmacokinetics/Drug Metab

Job Title:Assoc Prin. Scientist, Pharmacokinetics

Primary Location: NA-US-NJ-Madison

Employee Status: Regular

Travel: Yes, 10 % of the Time

Number of Openings: 1

Shift (if applicable): 1st

Company Trade Name:Merck
Datum: 25.05.2017


Lab Technician II, HIV Vaccine Trials

OverviewThe McElrath HIV Vaccine Trials Network (HVTN) laboratory is recruiting an entry-level laboratory technician to primarily perform assays characterizing T cell responses induced by vaccination.   S/he will be expected to prepare reagents and perform assays to evaluate vaccine-induced cellular immune responses in recipients participating in clinical trials of HIV investigational vaccines or other infectious diseases, such as malaria or TB.  S/he will be responsible for performing the assay...
Datum: 25.05.2017


Lab Technician II, Cell Processing

OverviewCures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred ...
Datum: 25.05.2017


Lab Technician II

OverviewCures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred ...
Datum: 25.05.2017


Principal Scientist - Computational Chemistry / Chemical Informatics

DescriptionCelgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health.  We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we look for talented people to grow our business, advance our science and contribute to our ...
Datum: 25.05.2017


Chemist (Shift) Job (Singapore, SG)

Chemist (Shift)-QUA005904

Description

Overview

- Responsible for planning, scheduling and performing laboratory testing of raw materials, packaging components, excipients, in-process control samples, intermediates, semi-finished products, final drug substances and finished products manufactured in API West, Biotech, Pharm West and Pharm South Facilities.
- Responsible for ensuring the analytical methods / specifications used are in accordance with requirements specified in MSD Quality Standards, regulatory dossiers and pharmacopoeia.
- Manage the calibration, maintenance and qualification of laboratory equipment.
- Conduct laboratory investigation on laboratory equipment failure, OOT and OOS.
- Responsible for testing of developmental and clinical products as required.
- Participate in analytical developmental activities as required.

Responsibilities

- Perform analytical testing on incoming raw materials, packaging components and excipients.
- Carry out testing activities associated with release and stability testing of the in-process control samples, intermediates, semi-finished products, final drug substances & finished products.
- Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures with necessary laboratory safety precautions.
- Carry out cleaning sample testing related to any equipment or facility cleaning activities.
- Co-ordinate with respective IPT facilities on the timing of drug substances change-over.
- Perform second person verification of other analysts’ work.
- Liaise and coordinate with external service providers in carrying out calibration/maintenance of lab equipment and tools when necessary.
- Carry out lab equipment calibration and proper documentation of all instruments in laboratories.
- Closely work with supervisor on the requirements of swabbing samples and to identify the appropriate sampling location and take swab samples for testing.
- Participate in analytical method transfer / validation and equipment Qualifications when necessary.
- Perform periodic reviews of existing cleaning method validation package & procedure, and to implement corrective actions for the periodic reviews.
- Assist in writing protocol to support method transfer/validation, compendial method verification and equipment qualifications when necessary.
- Conduct in Laboratory investigation using 5 whys & fishbone to identify the root cause and its report writing. Ensure laboratory related actions are effectively implemented within agreed time frame, to continually improve processes, prevent waste, and eliminate rework.
- Provides inputs to new Quality Standards and Standard Analytical Tests; implementing new Quality Standards once approved and obsoleting previous revisions
- Revise and write Standard Operating Procedures (SOPs) to reflect the current practice and ensuring that the current level of standard are met.
- Oversee Annual Product Review to ensure that the activities are completed by the required timelines
- Perform and maintain an acceptable level of good laboratory housekeeping.
- Maintain inventory and control in-house stock, reference standards, chemical reagents, and consumables and ensure that there are sufficient stocks for testing.
- Identify and execute laboratory efficiency improvement tasks, e.g., Kaizen.
- Any other duties as assigned by the Supervisor / Manager.

Qualifications

- Bachelor Degree in Chemistry/ Biochemistry.
- 0 – 3 years experience in pharmaceutical analysis is preferred.
- Experience in operating laboratory equipment such as Particle size analyzer, GC, HPLC, Karl Fischer Titrator is preferred.
Other Competencies and Personal Attributes:

- Effective written and verbal communication skills
- A good team player with ability to handle task independently
- Understands of the IPT value stream and customer focused
- Good time management skills
- Continuous improvement mindset
- Self-motivated with strong analytical skills
- Ability to coach, motivate and lead others through change
- Analytical development mindset in research and commercialization activities

Job: Quality Lab Related Job Title:Assoc. Spclst, Quality Control

Primary Location: APAC-SG-Singapore-Singapore

Employee Status: Regular

Travel: No

Number of Openings: 1

Company Trade Name:MSD
Datum: 24.05.2017


Senior Chemist Job (Singapore, SG)

Senior Chemist-QUA005338

Description

Overview

- Responsible for planning, scheduling and performing laboratory testing of raw materials, packaging components, excipients, in-process control samples, intermediates, semi-finished products, final drug substances and finished products manufactured in API West, Biotech, Pharm West and Pharm South Facilities.
- Responsible for ensuring the analytical methods / specifications used are in accordance with requirements specified in MSD Quality Standards, regulatory dossiers and pharmacopoeia.
- Manage the calibration, maintenance and qualification of laboratory equipment.
- Conduct laboratory investigation on laboratory equipment failure, OOT and OOS.
- Responsible for testing of developmental and clinical products as required.
- Participate in analytical developmental activities as required.

Responsibilities

- Perform analytical testing on incoming raw materials, packaging components and excipients.
- Carry out testing activities associated with release and stability testing of the in-process control samples, intermediates, semi-finished products, final drug substances & finished products.
- Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures with necessary laboratory safety precautions.
- Carry out cleaning sample testing related to any equipment or facility cleaning activities.
- Co-ordinate with respective IPT facilities on the timing of drug substances change-over.
- Perform second person verification of other analysts’ work.
- Liaise and coordinate with external service providers in carrying out calibration/maintenance of lab equipment and tools when necessary.
- Carry out lab equipment calibration and proper documentation of all instruments in laboratories.
- Closely work with supervisor on the requirements of swabbing samples and to identify the appropriate sampling location and take swab samples for testing.
- Participate in analytical method transfer / validation and equipment Qualifications when necessary.
- Perform periodic reviews of existing cleaning method validation package & procedure, and to implement corrective actions for the periodic reviews.
- Assist in writing protocol to support method transfer/validation, compendial method verification and equipment qualifications when necessary.
- Conduct in Laboratory investigation using 5 whys & fishbone to identify the root cause and its report writing. Ensure laboratory related actions are effectively implemented within agreed time frame, to continually improve processes, prevent waste, and eliminate rework.
- Provides inputs to new Quality Standards and Standard Analytical Tests; implementing new Quality Standards once approved and obsoleting previous revisions
- Revise and write Standard Operating Procedures (SOPs) to reflect the current practice and ensuring that the current level of standard are met.
- Oversee Annual Product Review to ensure that the activities are completed by the required timelines
- Perform and maintain an acceptable level of good laboratory housekeeping.
- Maintain inventory and control in-house stock, reference standards, chemical reagents, and consumables and ensure that there are sufficient stocks for testing.
- Identify and execute laboratory efficiency improvement tasks, e.g., Kaizen.
- Facilitate training of new recruits and generate the necessary training records and Analyst Qualification and Re-qualification Form (AQRF) for the trainee.
- Revise and write Standard Operating Procedures (SOPs) to reflect the current practice and ensuring that the current level of standard are met.
- Assist in responding to queries raised by regulatory agencies pertaining to analytical standards and methods.
- Assist in periodic review of laboratory procedures and ensure that current practices and standards are incorporated and reflected in the procedures.
- Responsible for release of batch results
- Supports Laboratory related metrics analysis and reporting
- Ensure all staff are appropriately trained and qualified to execute the duties assigned to them with respect to job, cGMP, GLP and SHE expectations as defined in the training matrix
- Schedule periodic review of test procedure to ensure the test methods and specifications are in line with current requirement specified in MSD Quality Standards, regulatory dossiers and pharmacopoeia.
- Work closely with global compendial group in reviewing of compendial changes and revise site test procedure and specification if necessary.
- Review of all the tests datasheet / worksheet records to ensure that the testing results are within SPC limits and meet Product Specification.
- Participate in SHE, Business Compliance, cGMP and all other compliance-related matters, where applicable.

Qualifications

- Bachelor Degree in Chemistry/ Biochemistry.
- 4 – 6 years experience in pharmaceutical analysis is preferred.
- Demonstrable experience and competency in Particle size analyzer, GC, HPLC, Karl Fischer Titrator, spectroscopic and wet chemistry testing is preferred.
- Demonstrated knowledge and application of sound scientific principles, theories, techniques and skills
- Technical competency in analytical troubleshooting.
- Demonstrated knowledge and understanding of cGMP, GLP, and associated regulatory expectations related to Pharmaceutical Analytical Testing and Release
- Potential to teach and coach the team on technical and business process elements of analytical testing.

Job: Quality Lab Related Job Title:Spclst, Quality Control

Primary Location: APAC-SG-Singapore-Singapore

Employee Status: Regular

Travel: No

Number of Openings: 2

Company Trade Name:MSD
Datum: 23.05.2017


Chemist (Biotech) Job (Singapore, SG)

Chemist (Biotech)-QUA005335

Description

Overview

- Responsible for planning, scheduling and performing laboratory testing of raw materials, packaging components, excipients, in-process control samples, intermediates, semi-finished products, final drug substances and finished products manufactured in API West, Biotech, Pharm West and Pharm South Facilities.
- Responsible for ensuring the analytical methods / specifications used are in accordance with requirements specified in MSD Quality Standards, regulatory dossiers and pharmacopoeia.
- Manage the calibration, maintenance and qualification of laboratory equipment.
- Conduct laboratory investigation on laboratory equipment failure, OOT and OOS.
- Responsible for testing of developmental and clinical products as required.
- Participate in analytical developmental activities as required.

Responsibilities

- Perform analytical testing on incoming raw materials, packaging components and excipients.
- Carry out testing activities associated with release and stability testing of the in-process control samples, intermediates, semi-finished products, final drug substances & finished products.
- Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures with necessary laboratory safety precautions.
- Carry out cleaning sample testing related to any equipment or facility cleaning activities.
- Co-ordinate with respective IPT facilities on the timing of drug substances change-over.
- Perform second person verification of other analysts’ work.
- Liaise and coordinate with external service providers in carrying out calibration/maintenance of lab equipment and tools when necessary.
- Carry out lab equipment calibration and proper documentation of all instruments in laboratories.
- Closely work with supervisor on the requirements of swabbing samples and to identify the appropriate sampling location and take swab samples for testing.
- Participate in analytical method transfer / validation and equipment Qualifications when necessary.
- Perform periodic reviews of existing cleaning method validation package & procedure, and to implement corrective actions for the periodic reviews.
- Assist in writing protocol to support method transfer/validation, compendial method verification and equipment qualifications when necessary.
- Conduct in Laboratory investigation using 5 whys & fishbone to identify the root cause and its report writing. Ensure laboratory related actions are effectively implemented within agreed time frame, to continually improve processes, prevent waste, and eliminate rework.
- Provides inputs to new Quality Standards and Standard Analytical Tests; implementing new Quality Standards once approved and obsoleting previous revisions
- Revise and write Standard Operating Procedures (SOPs) to reflect the current practice and ensuring that the current level of standard are met.
- Oversee Annual Product Review to ensure that the activities are completed by the required timelines
- Perform and maintain an acceptable level of good laboratory housekeeping.
- Maintain inventory and control in-house stock, reference standards, chemical reagents, and consumables and ensure that there are sufficient stocks for testing.
- Identify and execute laboratory efficiency improvement tasks, e.g., Kaizen.
- Any other duties as assigned by the Supervisor / Manager.

Qualifications

- Bachelor Degree in Chemistry/ Biochemistry.
- 0 – 3 years experience in pharmaceutical analysis is preferred.
- Experience in operating laboratory equipment such as Particle size analyzer, GC, HPLC, Karl Fischer Titrator is preferred.

Other Competencies and Personal Attributes:

- Effective written and verbal communication skills
- A good team player with ability to handle task independently
- Understands of the IPT value stream and customer focused
- Good time management skills
- Continuous improvement mindset
- Self-motivated with strong analytical skills
- Ability to coach, motivate and lead others through change
- Analytical development mindset in research and commercialization activities

Job: Quality Lab Related Job Title:Assoc. Spclst, Quality Control

Primary Location: APAC-SG-Singapore-Singapore

Employee Status: Regular

Travel: No

Number of Openings: 3

Company Trade Name:MSD
Datum: 23.05.2017


Chemist (API) Job (Singapore, SG)

Chemist (API)-QUA005534

Description

Overview

- Responsible for planning, scheduling and performing laboratory testing of raw materials, packaging components, excipients, in-process control samples, intermediates, semi-finished products, final drug substances and finished products manufactured in API West, Biotech, Pharm West and Pharm South Facilities.
- Responsible for ensuring the analytical methods / specifications used are in accordance with requirements specified in MSD Quality Standards, regulatory dossiers and pharmacopoeia.
- Manage the calibration, maintenance and qualification of laboratory equipment.
- Conduct laboratory investigation on laboratory equipment failure, OOT and OOS.
- Responsible for testing of developmental and clinical products as required.
- Participate in analytical developmental activities as required.

Responsibilities

- Perform analytical testing on incoming raw materials, packaging components and excipients.
- Carry out testing activities associated with release and stability testing of the in-process control samples, intermediates, semi-finished products, final drug substances & finished products.
- Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures with necessary laboratory safety precautions.
- Carry out cleaning sample testing related to any equipment or facility cleaning activities.
- Co-ordinate with respective IPT facilities on the timing of drug substances change-over.
- Perform second person verification of other analysts’ work.
- Liaise and coordinate with external service providers in carrying out calibration/maintenance of lab equipment and tools when necessary.
- Carry out lab equipment calibration and proper documentation of all instruments in laboratories.
- Closely work with supervisor on the requirements of swabbing samples and to identify the appropriate sampling location and take swab samples for testing.
- Participate in analytical method transfer / validation and equipment Qualifications when necessary.
- Perform periodic reviews of existing cleaning method validation package & procedure, and to implement corrective actions for the periodic reviews.
- Assist in writing protocol to support method transfer/validation, compendial method verification and equipment qualifications when necessary.
- Conduct in Laboratory investigation using 5 whys & fishbone to identify the root cause and its report writing. Ensure laboratory related actions are effectively implemented within agreed time frame, to continually improve processes, prevent waste, and eliminate rework.
- Provides inputs to new Quality Standards and Standard Analytical Tests; implementing new Quality Standards once approved and obsoleting previous revisions
- Revise and write Standard Operating Procedures (SOPs) to reflect the current practice and ensuring that the current level of standard are met.
- Oversee Annual Product Review to ensure that the activities are completed by the required timelines
- Perform and maintain an acceptable level of good laboratory housekeeping.
- Maintain inventory and control in-house stock, reference standards, chemical reagents, and consumables and ensure that there are sufficient stocks for testing.
- Identify and execute laboratory efficiency improvement tasks, e.g., Kaizen.
- Any other duties as assigned by the Supervisor / Manager.

Qualifications

- Bachelor Degree in Chemistry/ Biochemistry.
- 0 – 3 years experience in pharmaceutical analysis is preferred.
- Experience in operating laboratory equipment such as Particle size analyzer, GC, HPLC, Karl Fischer Titrator is preferred.
Other Competencies and Personal Attributes:

- Effective written and verbal communication skills
- A good team player with ability to handle task independently
- Understands of the IPT value stream and customer focused
- Good time management skills
- Continuous improvement mindset
- Self-motivated with strong analytical skills
- Ability to coach, motivate and lead others through change
- Analytical development mindset in research and commercialization activities

Job: Quality Lab Related Job Title:Assoc. Spclst, Quality Control

Primary Location: APAC-SG-Singapore-Singapore

Employee Status: Regular

Travel: No

Number of Openings: 1

Company Trade Name:MSD
Datum: 23.05.2017


Sr. Principal Scientist, Genetic Toxicology Job (West Point, PA, US)

Sr. Principal Scientist, Genetic Toxicology-RES001873

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its 125-year legacy. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases.

We are seeking a Sr. Principal Scientist to join the Genetic Toxicology group within the Investigative Laboratory Sciences Department in Safety Assessment and Laboratory Animal Sciences (SALAR), and to work part-time in the SALAR Program Development group. The primary responsibility of this position is to support (Q)SAR (quantitative structure-activity relationship) assessments of chemical structures for potential mutagenicity / genotoxicity to de-risk molecules in early discovery, and to help guide the overall genetic toxicology strategy. In this role, candidate will also be expected to work collaboratively with medicinal chemists, drug metabolism scientists, and with process and analytical chemists to support the ICH M7 guideline requirements on control of mutagenic impurities in pharmaceuticals. In addition to the genetic toxicology responsibilities, candidate will be expected to work part-time in the Program Development group to apply knowledge gain while at FDA to provide consultation on regulatory submissions and review of internal data packages for filing as well as serving as a Compound Leader for a drug development candidate(s). Compound Leader responsibilities include drug development strategy and risk assessment, SALAR representation on program teams, authoring regulatory and internal program-related documents, and interacting with regulatory authorities on issues relating to drug development candidate(s).

Qualifications

Education:

- Ph.D. in Toxicology with post-doctoral experience, at least 4 years of pharmaceutical industry experience, and at least 5 years of practical FDA experience as a pharm/tox reviewer.

Required:

- Strong knowledge of chemistry and metabolism of chemicals and pharmaceuticals in the context of toxicology and genotoxicity.

- Experience with the generation and interpretation of software (Q)SAR predictions. A minimum of 5 years practical FDA experience as a pharm/tox reviewer is required, including review of nonclinical PK/ADME, safety pharmacology, general toxicology, genetic toxicology, developmental and reproductive toxicology, and carcinogenicity.

- Excellent communication (oral and written) and collaboration skills.

Preferred:

- Experience and Skills - Knowledge of investigative and mechanistic toxicology of drugs.

Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need an accommodation for the application process please email us at staffingaadar@merck.com.

Search Firm Representatives Please Read Carefully:

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster

EEOC GINA Supplement?



Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Research Support Generic

Job Title:Sr. Prin. Scientist, Research

Primary Location: NA-US-PA-West Point

Employee Status: Regular

Travel: No

Number of Openings: 1

Shift (if applicable): N/A

Hazardous Materials: Standard lab materials

Company Trade Name:Merck
Datum: 23.05.2017


Synthetic Organic Chemist- Research Associate 1

Vertex, Abingdon, UK - May 19th
Datum: 19.05.2017


Synthetic Organic Chemist - Research Scientist 1

Vertex, Abingdon, UK - May 19th
Datum: 19.05.2017


Director Process Chemistry

Vertex, Boston, MA, USA - May 19th
Datum: 19.05.2017


Researcher (Physicist / Chemist)

Leibniz-Institut für Polymerforschung Dresden e. V.
Human Resources

Job offer No: 097/2017
The Institute Theory of Polymers at the Leibniz-Institut für Polymerforschung Dresden e. V. offers a Position for a

Researcher (Physicist / Chemist)

for the theory and simulation of polymernetworks.

This position allows to obtain a Ph.D. degree at the faculty of Mathematics and Science / theoretical Physics of the TU-Dresden under the guidance of Prof. Dr. J.-U. Sommer.

The Leibniz-Ins…


Datum: 19.05.2017


Project Manager for Open Science in Polymers 909682

A new open science collaboration between universities and industry has been established on Aarhus University. It is a collaboration inviting everybody in, thus right now we include companies ranging from large established companies to SMEs but all with an interest in smart polymer materials and nanocomposites. Based on industrial demands, basic research projects are defined.Students based at Department of Chemistry, iNANO, and AU Engineering work on the scientific part of the project and all col...
Datum: 19.05.2017


Postdoctoral Researcher in Synthetic Chemistry

Ming Wai Lau Centre for Reparative Medicine (MWLC) is established to further accelerate research in stem cell biology, biomedical engineering, biotechnology, and regenerative medicine. MWLC operates two nodes, one based at KI in Stockholm, Sweden and the other in Hong Kong, located in Science Park, Shatin. The Hong Kong node will include four research groups, initially consisting of a total of 20-30 scientists. Description of research group and projectDr. Linxian Li’s Laboratory has long interes...
Datum: 18.05.2017


Senior Team Leader in Medicinal Chemistry

Senior Team Leader in Medicinal Chemistry
Drug Discovery Unit, School of Life Sciences

Grade 9 (£49,772 – £55,998)

We are seeking a highly motivated and expert medicinal chemist for a key leadership role. The successful applicant will lead one of our major programmes, setting strategy, and ensuring goals and milestones are met. The appointee will line manage, and drive interactions between the medicinal chemists, biologists, computational chemists and the drug metabolism & pharmacoki…


Datum: 17.05.2017


ViiV CT Ph. D. Chemistry Position

GSK, Branford, CT, USA - May 16th
Datum: 16.05.2017


Chemistry Associate

GSK, Branford, CT, USA - May 16th
Datum: 16.05.2017


Lab Technician

Horizon Genomics is a biotechnology company in Vienna, Austria, that is part of the Horizon Discovery Group headquartered in Cambridge, UK. Using our proprietary gene-editing platform and deep scientific expertise, we design and engineer genetically-modified cells that are applied in research and clinical applications.  Our rapidly growing product catalog, service offering and research programs are powering progress to understand the genetics drivers of disease and ultimately advance human healt...
Datum: 16.05.2017


Investigator I/II, MedChem

Novartis, Shanghai, China - May 11th
Datum: 11.05.2017


2 Phd positions in nanostructures for Optoelectronics and Metamaterials

“2 Phd positions in nanostructures for Optoelectronics and Metamaterials”

Established in Agreement between Istituto Italiano di Tecnologia & Università degli Studi di Genova, Italy

1. Manipulating light emission with metamaterials

Metamaterials can lead to many exciting properties such as ultrahigh gain, negative refractive index, and directionally dependent dielectric permittivity. Hyperbolic metamaterials (HMMs) are a particularly interesting case that can be realized by alternating…


Datum: 10.05.2017


Chemist x2

Chemist x2 – Rushden
£Attractive Salary

Pharmaron is a premier R&D service provider for the pharmaceutical industry. Founded in 2003, Pharmaron has invested in its people and facilities, and established a broad spectrum of drug R&D service capabilities, ranging from synthetic and medicinal chemistry, biology, DMPK, pharmacology, safety assessment, radiochemistry and radiolabelled metabolism to chemical & pharmaceutical development. With about 4,000 employees and operations in China, the U…


Datum: 09.05.2017


Investigator, Medicinal Chemistry

Collegeville, PA, USA - May 9th
Datum: 09.05.2017


Senior Scientist, Green Chemistry

Stevenage, United Kingdom - May 9th
Datum: 09.05.2017


Medicinal/Synthetic Chemists (BS or MS)

Novartis, Cambridge, MA, USA - May 4th
Datum: 04.05.2017


Master Student / Recent Graduate (Internship)

Novartis, Basel, Switzerland - April 27th
Datum: 27.04.2017


Organic chemist / materials scientist: porous solids, cage molecules, ionic liq.

The Ameloot Group at the Center for Surface Chemistry and Catalysis (University of Leuven) is looking for a highly skilled organic synthetic chemist who wishes to expand his/her horizons to materials science. In consultation with the successful candidate, this project will focus on the synthesis and application of one or more of the following: (1) porous solids (e.g. metal-organic frameworks, MOFs), (2) organic 'porous' molecules (e.g. cage compounds) and (3) ionic liquids and derived materials….


Datum: 27.04.2017


Senior Scientist – Computational Medicinal Chemist

Are you up for a challenge? Do you look for ways to grow in your job? And do you want to build a phenomenal career? Then apply now! We’re currently looking for a:

Senior Scientist – Computational Medicinal Chemist

The objective of PMI’s R&D center is to develop and assess products with the potential to reduce the risks of smoking-related diseases. This project is at the core of our business: our vision is that one day all adult smokers who otherwise wouldn’t quit will switch to what we…


Datum: 12.04.2017


Full Professorship (W3) for Organic Chemistry - Functional Materials

The Faculty of Natural Sciences II – Chemistry, Physics and Mathematics – of the Martin- Luther-University Halle-Wittenberg invites applications for a

Full Professorship (W3) for Organic Chemistry – Functional Materials

The Faculty of Natural Sciences II (chemistry, physics and mathematics) focuses on research and teaching in the areas of „nanostructured materials“ with the main topics of „functional solid interfaces“ and „nanostructured polymers“ together with the areas of „photo…


Datum: 05.04.2017


Polymer Chemist (m/f)

Work group:Institut für BiomaterialforschungArea of research:Scientific / postdoctoral postsStarting date:1480636800Job description:Polymer Chemist (m/f)code no. 2016/B 29The place of employment is Teltow (near Berlin, Germany).The Helmholtz-Zentrum Geesthacht in Geesthacht, near Hamburg, and in Teltow, near Berlin, conducts materials and coastal research. For further information please refer to: www.hzg.de.The Institute of Biomaterial Science in Teltow of the Helmholtz-Zentrum Geesthacht and Be...
Datum: 02.12.2016




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