This post is also available in: Svenska (Swedish)

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