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: Associate, Production Scheduler, Cell Therapy Manufacturing
Location : Devens- MA
12 Hrs. Rotating Shift 1:00pm to 12:00am, therefore elegible for a 10% shift differential Key Responsibilities
- Point of contact for the Manufacturing Operations team to provide support, facilitating operational continuity and addressing issues as they arise and escalating if needed.
- Supports scheduling team in the creation and revision of the production plan/ schedule to meet product demand at the site.
- Supports equipment/ non-process needs of the Manufacturing Operations team on the floor.
- Supports collection of KPI and performance analytics.
- Work with Document Control to ensure all documents (e.g. batch records and packaging records) are ready for Manufacturing.
- Build strong relationships and communication with all functions.
- Provide exceptional customer service. Perform other tasks as assigned.
Qualifications & Experience
- 0-3 years' experience.
- Bachelor's Degree in relevant science, engineering or similar discipline preferred.
- 1+ years of scheduling experience in cGMP manufacturing environment preferred.
- Experience in scheduling cell therapy manufacturing preferred.
- Experience in material planning and/or finite scheduling in a medium to high volume environment, knowledge of scheduling platforms preferred.
- An equivalent combination of education, experience and training may substitute.
- Basic knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy (or related) manufacturing.
- Understanding of cell therapy and aseptic processing or lab techniques .
- Understanding of planning/ ERP (SAP) systems and analytics tools (RTMS/ Syncade) preferred .
- Experience in MS Office applications .
- Proficient written and verbal communication skills.
- Ability to work independently to meet objectives.
- Ability to work as a team.
- Attention to detail and ability to perform with a high degree of accuracy.
- Ability to identify and support strategies for continuous improvement.
- Solid analytical and problem-solving abilities
This position will be a 12hr shift on the Rotational schedule covering night time operations hours, with possibility of off-hours support to address scheduling constraints or questions as they arise.
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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.
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