Senior GMP Project Manager - 13530

Assignment Description:

We are looking for a Senior GMP Project Manager to join our dynamic team.

What you will work on:

Interpret GMP requirements based on internal procedures and applicable regulations.
Participate in the preparation and review of SOPs, handle referrals, and provide technical approvals.
Support validation, change, and decommissioning projects by reviewing and technically approving related documentation.
Write statements for deviation reports and investigations.
Stay updated on developments in computerized systems and validation, and inform or train others accordingly.
Participate in global information systems projects.
Perform technical approval of validation documents, change requests, deviation reports, and related documentation.

What you bring:

Expertise in computerized systems with at least 5 years of relevant experience.
University degree or equivalent experience in natural sciences, validation management, or process technology.
Extensive experience in the pharmaceutical industry, particularly in GMP-regulated environments.
Background in validation/QA, ideally as a CSV Engineer or QA-IT professional.
Strong understanding of industrial IT/OT and automation systems.
Excellent communication skills in Swedish and English, both written and spoken.

If this sounds interesting, please send your CV to cv@veritaz.se

Senior GMP Project Manager – 13530