Manager, Label Operations
Bristol Myers Squibb
June 30, 2026
On-site
Summit, NJ
Operations
Shift Available:
- Sunday–Wednesday, Onsite Night Shift, 6 p.m.–4:30 a.m.
Responsibilities:
- Lead Label Management and align with Global/Regional Regulatory requirements.
- Supervise label control activities for Cell Therapy Development and Operations (CTDO).
- Oversee/coordinate/prioritize daily Label Operations at the Summit, NJ S12 facility; maintain compliance.
- Ensure timely clinical/commercial label issuance for in-process and final products.
- Lead system implementation initiatives for clinical/commercial label management; support projects within timelines.
- Support new drug product launches and quality management activities; meet job objectives on time.
- Create development plans, assure staffing, onboard new staff, and coach/mentor subordinates.
- Support electronic label issuance/control systems.
- Write/review/update SOPs; manage archival of batch records and GMP documentation.
- Conduct gap assessments; develop/maintain quality metrics; collaborate to resolve quality system issues.
- Maintain current cGMP and global regulatory knowledge; perform supplemental investigations/projects as needed.
Knowledge & Skills:
- Advanced GMP, quality, compliance, and risk management; interpret issues and communicate clearly.
- Strong report authorship/review; apply Quality Risk Management principles.
- Action-oriented, customer-focused; strong decision-making, problem solving, planning, and relationship building.
- PC-based and Microsoft Office proficiency; minimal direction needed.
Minimum Requirements:
- B.S. degree (or equivalent education/experience).
- 5+ years relevant work experience.
- 2+ years leadership experience.
Compensation (Summit West, NJ, US): $103,560–$125,495 plus potential incentive cash/stock (eligibility-based).
Application instruction: If you’re intrigued but not a perfect resume match, apply anyway.
- Sunday–Wednesday, Onsite Night Shift, 6 p.m.–4:30 a.m.
Responsibilities:
- Lead Label Management and align with Global/Regional Regulatory requirements.
- Supervise label control activities for Cell Therapy Development and Operations (CTDO).
- Oversee/coordinate/prioritize daily Label Operations at the Summit, NJ S12 facility; maintain compliance.
- Ensure timely clinical/commercial label issuance for in-process and final products.
- Lead system implementation initiatives for clinical/commercial label management; support projects within timelines.
- Support new drug product launches and quality management activities; meet job objectives on time.
- Create development plans, assure staffing, onboard new staff, and coach/mentor subordinates.
- Support electronic label issuance/control systems.
- Write/review/update SOPs; manage archival of batch records and GMP documentation.
- Conduct gap assessments; develop/maintain quality metrics; collaborate to resolve quality system issues.
- Maintain current cGMP and global regulatory knowledge; perform supplemental investigations/projects as needed.
Knowledge & Skills:
- Advanced GMP, quality, compliance, and risk management; interpret issues and communicate clearly.
- Strong report authorship/review; apply Quality Risk Management principles.
- Action-oriented, customer-focused; strong decision-making, problem solving, planning, and relationship building.
- PC-based and Microsoft Office proficiency; minimal direction needed.
Minimum Requirements:
- B.S. degree (or equivalent education/experience).
- 5+ years relevant work experience.
- 2+ years leadership experience.
Compensation (Summit West, NJ, US): $103,560–$125,495 plus potential incentive cash/stock (eligibility-based).
Application instruction: If you’re intrigued but not a perfect resume match, apply anyway.