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Associate Director of Validation

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Bristol Myers Squibb
Full Time position
Listed on 2025-12-25
Job specializations:
  • Engineering
    Pharma Engineer, Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 164838 - 199745 USD Yearly USD 164838.00 199745.00 YEAR
Job Description & How to Apply Below
Location: Indianapolis

Associate Director of Validation
, Bristol Myers Squibb

Location:

Indianapolis, IN

Employment Type:

Full-time

Working with Us

Challenging, meaningful, life‑changing work. At Bristol Myers Squibb, you’ll contribute to transforming patients’ lives through manufacturing and cell therapy innovation. Join high‑achieving teams, grow career opportunities, and balance flexibility with strong benefits.

Key Responsibilities
  • Lead, plan, and execute the validation strategy for manufacturing facilities, utilities, equipment, process technologies, and computerized systems.
  • Develop and oversee validation master plans, protocols (IQ/OQ/PQ), and reports for new or expanded manufacturing capabilities.
  • Direct and coordinate multidisciplinary validation teams, including hiring, mentoring, and professional development of validation personnel.
  • Collaborate closely with site leadership, engineers, QA/Quality, and external vendors and contractors to ensure timely and compliant validation delivery for expansion, renovation, and site build projects.
  • Ensure adherence to budget, schedule, and quality standards within validation scope across all site projects.
  • Review and approve technical documentation, validation protocols, risk assessments, and qualification deliverables.
  • Manage and resolve deviations, CAPAs, and change controls related to validation and qualification activities.
  • Support regulatory inspections, audits, and responses by ensuring site validation compliance and document integrity.
  • Lead validation efforts to support site/facility strategic initiatives, new technology integration, and global harmonization as needed.
  • Drive continuous improvement of validation processes for enhanced site reliability and regulatory compliance.
  • Lead and mentor the deviation investigations team for the site.
  • Uphold all safety standards; ensure safe handling of radioactive materials and hazardous equipment throughout validation activities.
Education and Experience
  • Required:

    Bachelor’s degree in Engineering, Life Sciences, or related discipline.
  • Preferred:
    Advanced degree or professional certification in validation (e.g., IVT, PDA, or equivalent).
  • Minimum 8 years’ experience in validation within pharmaceutical/radiopharmaceutical manufacturing, including large‑scale capital project support (>$10M).
  • Demonstrated understanding and hands‑on experience with radiopharmaceutical or pharmaceutical validation systems and compliance.
  • Direct experience managing validation or multidisciplinary project teams and external contractors.
Skills and Qualifications
  • Strong knowledge of pharmaceutical validation practices, including cGMP and FDA/USP/OSHA regulatory requirements.
  • Expert understanding of facility, utility, aseptic processing, and fill/finish equipment validation.
  • Advanced proficiency in authoring and managing validation documentation (master plans, risk assessments, protocols, and reports).
  • Familiarity with qualification of computerized systems and data integrity best practices.
  • Solid background in vendor management, contract review, and cost controls within validation scopes.
  • Excellent written, verbal, stakeholder, and team leadership communication skills.
  • Proficient in MS Office Suite, validation software/applications, and computerized maintenance management systems (CMMS).
  • Willingness to work in radioactive environments and follow strict safety requirements.
  • Ability to travel and support validation at multiple domestic or international sites.
Physical Demands
  • Ability to climb ladders and lift up to 25 lbs.
  • Frequent interaction within laboratory or manufacturing settings; PPE required in controlled environments.
Work Environment
  • Moderate noise levels.
  • Exposure to laboratory, pharmaceutical manufacturing, and radiopharmaceutical production areas.
Compensation Overview

Indianapolis – Rayze Bio – IN $164,838 – $199,745 FTE basis. Additional incentive cash and stock opportunities may be available. Final compensation will be decided based on demonstrated experience.

Benefits
  • Health Coverage – Medical, pharmacy, dental, and vision care.
  • Well‑being Support Programs – BMS Well‑Being Account, BMS Living Life Better, Employee Assistance Programs (EAP).
  • Financial Well‑being – 401(k)…
Position Requirements
10+ Years work experience
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