Validation Lead Pharmaceutical Manufacturing 17682
Veritaz ABPublicerad: 2026-05-13
Ansök senast: 2026-06-12
Beskrivning
Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.
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
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
