Senior Validation Engineer - 12859

Assignment Description:

We are looking for a Senior Validation Engineer to join our dynamic team.

What you will work on:

Validate a new pharmaceutical manufacturing process, ensuring compliance and robustness
Lead and execute change management activities related to the new process
Perform PQ/PV (Performance Qualification/Process Validation) of the manufacturing process
Adjust items and manufacturing orders in SAP and PAS-X to align with process requirements
Conduct GMP and SHE risk reviews to ensure safety, quality, and regulatory compliance
Collaborate closely with cross-functional teams to secure progress and effective knowledge transfer
Contribute to continuous improvement initiatives, supporting an environment with a high rate of change and digitalization

What you bring:

University-level technical or scientific education with a focus on chemistry
Extensive experience in pharmaceutical manufacturing within GMP-regulated environments
Proven experience as a validation engineer and process engineer
Strong adaptability and flexibility, with the ability to manage changes in dynamic projects
Proficiency in both Swedish and English, with excellent communication skills in speech and writing
Ability to share knowledge effectively and lead cross-functional groups toward project goals
A proactive, driven, and outgoing mindset, thriving in fast-paced and digitalized environments
Desirable knowledge and experience in qualification, validation, GMP, LEAN, and continuous improvement work

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

Senior Validation Engineer – 12859