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Working with Us

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 rich in diversity. 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: careers.bms.com/working-with-us.

Our Clinical Supply Operations is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely, efficiently and on time while operationalizing the innovative technologies that will deliver the transformative medicines of tomorrow. As a member of our team, you will get the chance to play a pivotal role to positively impact patients’ lives while developing professionally to achieve your own career goals.

Position Summary 

The Clinical Supply Operations (CSO) department located in New Brunswick, NJ drives innovation by implementing new manufacturing technologies and processes to support our future portfolio. We are seeking an experienced individual contributor to join our Facilities and Engineering Support team who possesses strong knowledge of OSHA regulations applicable to pharmaceutical manufacturing, EHS compliance, Risk Management, and knowledge of Industrial Hygiene concepts. Ideal candidate will also have understanding of basic engineering principles and project management skills. 

This position is responsible for the evaluation and mitigation of manufacturing process-related risks related to equipment, facilities, and utilities; provides guidance for capital engineering projects impacting the department, mitigation of product exposure, and broader worker safety directives related to facilities maintenance and equipment. The candidate will support the broader Clinical Supply Operations department in implementing, developing, initiating, and sustaining EHS programs.

Key Responsibilities 

  • Role will be primarily responsible for managing and sustaining the CSO Manufacturing Process Safety management program.
  • Provides PSM leadership, technical support and direction for Clinical Supply Operations Facilities and Engineering Support (Capital and Department based) projects.
  • Maintains working knowledge and understanding of CSO manufacturing facilities, equipment, systems, campaigns, operations, and schedule.  
  • Serves as the CSO liaison for global and site EOHSSS related activities, programs, initiatives, and committees as assigned.
  • Serves as the EHS and Industrial Hygiene subject matter expert for CSO personnel.  
  • Creates, manages, and reviews, department-specific health and safety policies and programs as needed for currency and applicability.  
  • Acts as a liaison to the site Emergency Response Team for CSO NBR emergencies.  
  • Serves as investigator for CSO Process Safety Management (PSM) incidents and near misses. Oversees the management and delegation of non-PSM CSO NBR safety incidents and near misses.
  • Partners with CSO (and broader site) functional area representatives for incident investigations, CAPA, initiatives and projects.
  • Creates content and conducts training programs for process safety related activities and relevant EHS topics.  
  • Participates in developing CSO safety goals and objectives in alignment with NBR site and Global Pharmaceutical Sciences & Development safety / environmental / occupational health guidance.
  • Provides leadership for creating a responsible and sustainable safety culture for CSO.  
  • Evaluates new technologies and new materials /processes introduced into departments.  
  • Responsible for evaluating regulatory and internal policy change that will affect CSO equipment, building, and processes.  
  • Serves as the CSO NBR contact for environmental/safety internal and external regulatory audits and inspections.   
  • Manages the internal CSO safety self-inspection process, corrective actions, continuous improvement efforts and departmental metrics reporting.  
  • Supports and performs industrial hygiene monitoring/sampling and results analysis / reporting.  
  • Provides support for the CSO contractor safety program, including administrating Safe Work Permits and Job Hazard Analysis reviews as required.  
  • Manages the departmental license for CSO radio-pharmaceutical work at New Brunswick, NJ site.  

Qualifications & Experience 

  • Bachelor's degree in Engineering, Sciences, Occupational Health, Environmental Science.  
  • 7+ years of related experience in the EHS field, preferably in a manufacturing, R&D or production environment for the biotech/pharmaceutical industry.
  • Previous experience in Manufacturing Process Safety Management including participating in and/or leading Process Hazard Analysis (PHA) is highly desirable.  
  • Experience in supporting Facilities Operations (LO/TO, working from heights, electrical classification, ability to read schematics) and Manufacturing Operations (handling and containment of highly potent drugs, equipment containment operations).
  • Knowledge of U.S. Environmental, Health and Safety regulations and disciplines is desired.  
  • CSP (Certified Safety Professional), CIH (Certified Industrial Hygienist), Certified Hazardous Materials Manager (CHMM) desirable.  
  • General understanding of hazardous waste rules, regulations, and management.  
  • Strong interpersonal, presentation and communication skills; with the ability to communicate effectively to influence and engage others in safe behaviors and practices.  
  • Ability to work independently, contribute within a team, and actively engage and partner with other functional area colleagues.  
  • May work on assignments that are complex in nature where independent action and a high degree of initiative are required in resolving problems and developing recommendations and driving efforts to completion.   

#LI-Onsite

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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Confirmed 8 hours ago. Posted 30+ days ago.

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