Manager, Principal Compliance Engineer

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.

This is work that transforms the lives of patients, and the careers of those who do it.

The Principal Compliance Engineer, Equipment Commissioning & Qualification (ECQ), supports the successful operation of facility, laboratory, and business functions at Summit, NJ. This role involves interaction with internal team members, peer-level customers, and external service providers. The Principal Compliance Engineer will lead a team of contract or full-time personnel responsible for performing periodic reviews of equipment, policies, and procedures to ensure they remain in a validated state.

Responsibilities include performing gap analyses, and leading small and large-scale projects to achieve departmental objectives.

• Advanced knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21
  
  CFR part 11, computer systems validation requirements, and good documentation practices.
• Advanced understanding of pharmaceutical, manufacturing, and laboratory systems and equipment.
• Strong attention to detail.
• Exceptional written and verbal communication skills.
• Excellent interpersonal skills; experience working with a inclusive workforce.
• Proven multi-tasking and organizational skills; ability to manage multiple concurrent assignments in a high-paced environment.
• Strong presentation development and delivery skills.
• Highly proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and extensive background in database systems.
• Ability to quickly learn new software, such as corporate intranet and enterprise business applications.
• Ability to organize and present information clearly.

• BS in Engineering or Science-related discipline is required.
• Minimum of 5 years’ experience in an FDA-regulated industry.
• 2 years’ experience in a quality assurance-related discipline preferred.
• In-depth knowledge of regulatory guidelines (FDA, EMA, USP, EP, JP).
• Excellent computer skills, including knowledge of calibration management and environmental monitoring systems.
• Strong verbal and written communication skills; able to work independently.
• Must possess strong interpersonal and communication skills, be a team player, and demonstrate professional maturity, initiative, and accountability.

Ensure Equipment Compliance:
Ensure all equipment and technologies at Bristol Myers Squibb comply with local, global, and regulatory policies, procedures, and guidelines. Review and implement revisions to USP, EP, JP, FDA, and regulatory guidelines. Perform gap analyses on existing equipment and technologies. Review new equipment and technologies to ensure compliance.

Ensure ECQ Departmental Compliance:
Participate in revisions of departmental procedures to maintain compliance. Ensure departmental procedures and policies are aligned with current local, global, and regulatory requirements. Historical Performance Review (HPR) and Compliance Project Support or lead HPR on-demand board meetings and investigations/deviations.

Compliance Projects:
Identify, scope, lead, and support projects of varying complexity to maintain equipment and departmental compliance.

Regulatory Responsibilities:
Parti…