Validation Engineer

Bristol Myers Squibb UK

Bothell, WA, United States
Bothell - wa - us: $83,220 - $100,847; not specifi...
On-site
Gmp asset management and validation
Regulated gmp manufacturing facility
Validation protocols, risk assessments, and qualification plans
Bristol Myers Squibb is seeking a Validation Engineer for their Bothell, WA location. This role focuses on ensuring compliance with regulatory standards in a GMP manufacturing environment, requiring hands-on experience in validation processes and equipment qualification

Job Summary

  • The Validation Engineer will play a critical role in ensuring compliance with all regulatory requirements and industry standards related to GMP asset management and validation in a regulated GMP manufacturing facility.
  • This position requires a hands-on validation engineer with experience in GMP, an understanding of lab/manufacturing equipment, and a proven track record in validation processes.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment and offers a wide variety of competitive benefits, services and programs.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Validation Engineer for their Bothell, WA location. This role focuses on ensuring compliance with regulatory standards in a GMP manufacturing environment, requiring hands-on experience in validation processes and equipment qualification.

Salary

Bothell - WA - US: $83,220 - $100,847; Not specified; Health Coverage: Medical, pharmacy, dental, and vision care.

Skills & Requirements

Must-have

  • GMP asset management and validation
  • regulated GMP manufacturing facility
  • validation protocols, risk assessments, and qualification plans
  • validation Subject Matter Expert (SME)
  • regulatory agencies during inspections and audits

Nice-to-have

  • foster a culture of compliance
  • drive innovation and improvement
  • proactively supports other team members

Key Requirements

  • Bachelor’s Degree in life sciences/engineering/STEM or equivalent
  • 2+ years of commissioning, qualification, and validation (CQV) experience
  • Robust knowledge of cGMP, GDP, GXP, GAMP5 regulations
  • Experience with equipment/utility/facility qualifications
  • Excellent project and program management, communication skills, and technical writing skills

Work Rights

Not specified

Tailored Resume

Cover Letter