Stays updated with regulatory and quality standards, evolutions in GXP compliance and best practices where needed everywhere in the world
Performs required Method validation, verification, transfer and stability samples analytical work and fills out relevant documentation, including generating reports and filling CoAs.
Performs request, label and management of assigned products process validation batches and stability samples for the new geographical and presentations filings.
Supports the management of critical documents and CAPA in addition to the preparation of quality management and audit reviews
Acts as primary contact for the related sites to support the introduction of assigned products for the identified purpose
Ability to remain update in all analytical techniques required.

Bachelor’s degree in in chemical engineering, chemistry or similar;
Demonstrated knowledge of working in an analytical lab environment, of the cGMPs, and should have the ability to follow SOPs and policies;
Demonstrated ability and skill to perform required analytical techniques and to operate and troubleshoot the associated equipment and software;
Capability of working with others and as part of a team is essential;
Good problem-solving techniques is needed to make necessary adjustments and to prioritize tasks.

Analyst, Pharmaceutical Development

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