Be a part of the Analytical Science and Technology Team.
Lead the transfer and or co-validation of analytical methods in contract lab organizations (CLO) in close collaboration with internal experts on the analytical technologies.
Act as primary contact for the CLO, gather information and data generated at the CLO’s and evaluate against available internal data for existing or new production processes.
Plan the analytical project(s) in your responsibility, identify risks and report progress & risks to the analytical team and governance bodies.
Maintain, adjust, and communicate documentation and knowledge.
Write and review transfer/co-validation protocols and reports.
Support dossier submission activities with regards to analytical aspects.
Requirements
You have a PhD in Life Sciences or are equivalent through experience.
You have expertise in method transfer and validation in a GMP and non-GMP environment in accordance with current industry practices.
You have an excellent analytical problem-solving mindset (escalate when needed) and can handle multiple tasks at the same time.
You have good technical writing skills and are able to prepare protocols and reports. As well as drawing up realistic project plan for method transfer/validation.
Expertise in analytical technology (e.g. spectrophotometry, biological activity, potency binding ELISA, BIAcore, Octet, …) is a plus.
You have the ability to work accurately while maintaining a strong focus on results and exhibiting a quality-oriented mindset.
You have the ability to critically analyze data, draw scientifically sound conclusions, and formulate them correctly.
You have excellent knowledge of cGMP and can convert legal requirements regarding analytical methods into effective action plans.
You are a team player and have good communication skills.
You are flexible, stress-resistant, open to change & innovation, and used to working within deadlines.
You are willing to adapt to changing priorities and willing to learn at a rapid pace.
Travel might be required as part of this role (up to 10% of the time)