This post is also available in: English (Engelska)

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