Quality Control Environment Monitoring Supervisor

Quality Control Environment Monitoring Supervisor

Join to apply for the Quality Control Environment Monitoring Supervisor role at Bristol Myers Squibb
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Challenging. Meaningful. Life‑changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:

• Manage EM program
  • Supervise EM technicians/analysts performing viable, non‑viable, personnel, settling plates monitoring in ISO‑classified and controlled spaces.
  • Schedule routine and non‑routine EM activities to support manufacturing operations and facility readiness.
  • Oversee execution of environmental and utility sampling including microbial identification workflows.
  • Ensure laboratory activities follow SOPs, aseptic techniques, gowning procedures and safety requirements.
  • Review and/or approve EM data, escalating excursions.
  • Lead or support investigations for EM‑related investigations, including root cause analysis and CAPA development to ensure timely close‑out.
  • Ensure EM program documentation such as SOPs, forms, maps are current and audit‑ready.
  • Ensure EM trending, monthly/quarterly reports are performed in a timely manner.
  • Approval of SOPs, trend data, investigations, non‑conformances, validation protocols, reports, validation/verifications and equipment qualifications.
  • Develop and maintain appropriate documentation, particularly data analysis and team KPI’s.
• Team Management
  • Supervise a team of EM technicians/analysts.
  • Assign tasks and prioritize workload to ensure timely completion of work in an on‑time and right‑first‑time manner.
  • Foster a positive and collaborative work environment within the lab and with external stakeholders both within the site and outside the site.
  • Coach team members, conduct performance evaluations and support career development.
• Continuous Improvement
  • Support continuous improvement programs for EM such as new EM technologies and improve data visibility.
  • Identify other opportunities for process improvements and implement changes to increase quality and efficiency within the Quality Control laboratories.
• Release of isotope, product and other studies
  • Collaborate with Manager and/or Reviewer to ensure all documentation for release is reviewed.
  • Work with Manager and/or Investigation Writer to ensure any discrepancies are resolved in a timely manner.
• Quality Assurance/Regulatory Compliance
  • Assist in the routine calibration and maintenance of laboratory equipment. Ensure schedule compliance to ensure GMP readiness.
  • Work with Quality Assurance and Management to implement internal audits.
  • Participate in troubleshooting of issues and implement corrective actions to improve quality processes as a result of investigations or internal audits.
• Work with RSO and QA to ensure compliance with GMP regulations, safety guidelines, and quality standards (FDA, USP, NRC, EP, and other regulatory agencies as needed).
• Weekend work, early starts, or late ending times may be required.
• Up to 10% of travel may be required.
• Education and Experience
  • BS in microbiology or related field with 5+ years of direct radiopharmaceutical experience or 5+ years of experience in pharmaceutical field, OR MS in microbiology or related field with 5+ years of experience in pharmaceutical field.
  • At least a year of supervisory experience.
  • A strong background in microbiology and aseptic manufacturing is required.
• Preferred Experience
  • Experience in radiopharmaceutical field.
  • Experience handling radioactive…