Research Analyst - QC

Location: Haarlem, North Holland Salary: competitive
Sector: Life Sciences, Upstream, Downstream and Chemicals Type: contract

Progressive is looking for a professional who can join The Quality Control Innovative Laboratory where you'll be responsible for transfer, validation and verification of analytical methods for testing of new drug products in the laboratory. Other responsibilities embrace the Method compliancy, development and remediation.

Job Title - Research Analysts QC Complex drug products

As research analyst QC, you will be responsible for developing & validating analytical methods to obtain reliable and robust release testing procedures. Furthermore, the research analyst is involved in non-routine analyses to support investigations as well as the support of submission -related activities for new product introductions into the production department. Taking into account the experience with complex product testing it is considered that the Research analyst Complex drug product may act as key-expert in trouble-shooting analytical challenges with this type of products.

Key activities
* Perform complex testing
* Development, transfer, validation, verification and/or remediation of analytical methods
* Writing of protocols & reports
* Maintain adherence to corporate policies and appropriate regulations through actions and decisions
* Active participation in advanced problem solving, root cause analysis, troubleshooting, interpretation/consultation, verification of quality and test results discussions
* First-line Troubleshooting of laboratory equipment, aides in maintenance and certification of test instruments and apparatus to ensure compliance.
* Active participation in changes or act as change owner as part of continuous improvement.

Your Profile
* Bachelor degree in analytical chemistry/pharmacy or equivalent experience
* Knowledge and familiarity with the use of Pharmacopoeia methods
A strong analytical oriented mindset.
Experience with working in a pharmaceutical environment
Experience with analytical methods for complex drug products (e.g containing liposomes, proteins, microparticles) is a preference
Experience with UPLC, CD, PSD, FFF is a preference
Good knowledge of Pharmaceutical quality systems and production processes
Team player, but able to work independtly without minimal guidance
Experience with writing procedures is a plus

If this position is something that you want to do, and if you believe you have the right qualifications and experience required for the role, please do not hesitate and send us an e-mail with your most recent CV and short motivation letter to: j.vanbaalen(@)