Company

Bristol-Myers Squibb CompanySee more

addressAddressNew Brunswick, NJ
type Form of workFull-Time
CategoryManufacturing

Job description

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.
Position Summary
This position is responsible for the evaluation and mitigation of process-related risks related to facilities, engineering projects, product exposure, equipment, etc.
Key Responsibilities
  • Role will be primarily responsible for managing and implementing the CSO Process Safety management program.
  • Provide PSM leadership, technical support and direction for Clinical Supply Operations Facilities and Engineering Support (Capital and Department based) projects.
  • Maintain working knowledge and understanding of CSO manufacturing campaigns, equipment, systems, facilities, and operations.
  • Serves as CSO liaison for global and site EOHSSS related activities, programs, and committees as assigned.
  • Serve as an EHS subject matter expert for CSO personnel.
  • Create, manage, and review, department-specific health and safety policies and programs as needed.
  • Acts as a liaison to the site Emergency Response Team for CSO NBR emergencies. .
  • Act as a lead 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.
  • Create and conduct training programs for Process Safety related activities and relevant EHS topics.
  • Participate in developing CSO safety goals and objectives in alignment with NBR site and Global Pharmaceutical Sciences & Development safety / environmental / occupational health guidance.
  • Provide leadership for creating a responsible and sustainable safety culture for CSO.
  • Evaluate new technologies and new products/processes introduced into department.
  • Responsible for evaluating regulatory and internal policy change that will affect CSO equipment, building, and processes.
  • Serve as the CSO NBR contact for environmental/safety internal and external regulatory audits.
  • Manage the internal CSO safety self-inspection process, corrective actions, and departmental metrics reporting.
  • Manage the departmental license for CSO radio-pharmaceutical work at New Brunswick, NJ site.
  • Support and perform industrial hygiene monitoring/sampling and analyze results.
  • Provides support for the CSO contractor safety program, including administrating Safe Work Permits and Job Hazard Analysis reviews as required.

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 Process Safety Management including participating in and/or leading PHAs is highly desirable.
  • Experience in supporting Facilities Operations (LO/TO, working from heights, electrical classification, ability to read schematics) and Manufacturing Operations (handling 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.
  • Excellent interpersonal, presentation and communication skills, with the ability 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.

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.
Refer code: 7714237. Bristol-Myers Squibb Company - The previous day - 2024-01-05 15:33

Bristol-Myers Squibb Company

New Brunswick, NJ

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