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.
Job Summary:
The Manager, Parenteral Manufacturing is responsible for aseptic operations and GMP production floor supervisory responsibilities. These responsibilities will include, but are not limited to, general oversight and maintenance of readiness of the facility and equipment for use in production, change management and process improvement efforts on the production floor, and supervisory responsibilities during batch execution. The individual will strive for 'right the first time' quality of operations and maintain a high level of GMP awareness and compliance.
Role & Responsibilities:
- Support manufacturing activities in a supervisory capacity for execution and during documentation review and approval process. Maintain oversight of the GMP production facility for cleanliness, condition, and removal of expired materials. Track and assure all pre-requisites for batch manufacturing are released and available as needed.
- Assist in the manufacture of pharmaceutical parenteral drug products for use in clinical studies. Operations are carried out in a cGMP compliant manner in a controlled cleanroom environment with strict adherence to OSHA safety requirements, standard operating procedures (SOP's) and production batch records.
- Follow all relevant procedures, batch records and protocols as required. Ensure procedural and regulatory compliance of yourself and all operations personnel on the production floor.
- Review and revise procedures, protocols and batch records as needed to simplify and gain operational efficiency while maintaining a regulatory compliant process.
- Perform all required deviations, corrective actions and change controls within specified time limits.
- Participate in continuous improvement efforts targeted to simplify and streamline operations and/or add process capability. Identify opportunities for continuous improvement within the department, initiate projects to implement continuous improvement changes.
- Build strong relationships and collaborate effectively with peers within the functional area and across broader organizations. Drive delivery of functional area, project, and broader organizational-owned commitments.
- Ensure all relevant training is completed on time. Supports training and qualification of CSO-PAR production staff.
- Maintain aseptic process training and knowledge according to local procedures, policies and trainings. Maintain a deep understanding of cGMP's as they relate to evolving domestic and international regulatory standards coupled with an awareness of new industry developments and trends.
- Establish and maintain a safe work environment for self and co-workers. Ensure all safety requirements are being maintained within the production facility. Support safety area reviews and investigations of safety events that occur.
- Support all ongoing manufacturing equipment qualification/re-qualification activities.
- Identify and escalate technical and/or business issues promptly and provide potential solutions for consideration.
- Establish effective plans for projects and assign workloads to meet designated timelines. Prioritize work and use resources to meet designated timelines.
- Communicate directly, openly, and honestly.
Experience & Qualifications:
- Bachelor's Degree in a science or engineering field
- Minimum of five (5) years of experience working in GMP manufacturing areas.
- Experience working with sterile biologic drug products in a controlled cleanroom environment is preferred.
- Proficiency in use of computer programs/systems is essential.
Why You Should Apply
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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.
Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or 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.
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
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
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.
