Assignment Description
We are looking for an experienced Validation Lead with strong experience from the pharmaceutical industry and GMP-regulated manufacturing environments.
What You Will Work On
- Lead and support validation activities for pharmaceutical production equipment
- Develop validation protocols and validation reports
- Ensure validation documentation is complete, accurate, and compliant
- Support qualification and validation processes within manufacturing environments
- Collaborate closely with production, quality, and engineering teams
- Contribute to regulatory and GMP-compliant validation activities
- Support troubleshooting and problem-solving related to validation processes
- Participate in continuous improvement initiatives within validation and production
- Ensure delivery of validation activities according to project timelines and quality requirements
What You Bring
- University degree within Engineering, Science, or a related technical field
- Experience working within aseptic manufacturing environments
- Experience from pharmaceutical manufacturing and GMP-regulated operations
- Proven experience working as a Validation Engineer or Validation Lead
- Strong experience writing validation protocols and validation reports
- Good understanding of qualification and validation processes
- Ability to work independently in fast-paced production environments
- Strong problem-solving skills with a hands-on and solution-oriented mindset
- Flexible and adaptable approach within changing project environments
- Strong result-oriented mindset and ability to manage priorities effectively
- Excellent communication skills in both Swedish and English, spoken and written
If this sounds interesting please send your CV at cv@veritaz.se
