Supervisor – Finished Drug Product Production
Job Responsibilities
Provide day-to-day operational oversight of radio Finished Drug Product production activities, including scheduling, material preparation, line clearance, equipment setup, and batch record execution, ensuring compliance with GMP, NRC regulations, and internal expectations.
Serve as a functional lead for production operators by providing guidance, task coordination, and on-the-floor support to ensure safe, compliant, and efficient execution of manufacturing activities.
Support onboarding and training efforts for production staff and promote adherence to GMP and radiation safety best practices during manufacturing activities.
Support and execute validation activities associated with Finished Drug Product production at the clinical and commercial scale.
Collaborate with cross-functional partners including Quality, Safety, Engineering, Development, and Global Supply Chain to identify opportunities for process optimization, troubleshooting, and continuous improvement.
Assist Finished Drug Product Production Management with the compilation of operational KPIs and support the investigation and resolution of quality events (e.g., deviations, OOS, and nonconformances).
Support inventory management activities, including consumables, spare parts, cleaning supplies, and personal protective equipment (PPE).
Promote and reinforce a strong culture of safety, quality, and compliance with EHS and Radiation Safety programs.
Author, review, and revise production technical documentation (e.g., SOPs, forms, batch records) as needed to support manufacturing operations.
Requirements
High school diploma or equivalent.
Minimum of 5 years of relevant experience in pharmaceutical manufacturing, preferably in a cGMP environment.
Experience with radiochemistry and/or radiopharmaceuticals is preferred.
Knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory requirements.
Strong organizational and problem-solving skills.
Ability to work independently and as part of a team.
Excellent communication and interpersonal skills.
Qualifications
Bachelor's degree in a relevant field such as chemistry, biochemistry, or engineering.
Preferred certifications in GMP, HACCP, or similar regulatory standards.
Experience with process validation and troubleshooting.
Experience with regulatory submissions and compliance.
Skills
Strong understanding of radiochemistry principles and techniques.
Proficiency in Microsoft Office Suite.
Ability to work effectively in a fast-paced, dynamic environment.
Benefits
Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support Programs: BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Pay
$107,904 - $130,754
Schedule
Full-time