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Devens, Massachusetts, United States Bristol-Myers Squibb Full timeAbout UsAt Bristol Myers Squibb, we redefine the meaning of work. Here, every day presents an opportunity to engage in challenging and impactful projects that significantly affect patients' lives. From enhancing production processes to pioneering advancements in cell therapy, our work is transformative for both our patients and our employees. We provide an...
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Devens, Massachusetts, United States Bristol-Myers Squibb Full timeJoin Our TeamAt Bristol Myers Squibb, we redefine the workplace experience. Our environment is not just about tasks; it’s about making a significant impact. Here, you will engage in work that is both challenging and transformative, contributing to breakthroughs in cell therapy that change lives. You will have the opportunity to develop your career in a...
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Devens, United States Bristol-Myers Squibb Full timeWorking 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...
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Devens, Massachusetts, United States Bristol-Myers Squibb Full timeJoin Our TeamAt Bristol Myers Squibb, we redefine the concept of work. Here, you will engage in impactful and rewarding endeavors that go beyond the ordinary. Our environment fosters innovation and collaboration, where every day presents unique challenges that contribute to significant advancements in cell therapy. You will have the opportunity to develop...
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Devens, Massachusetts, United States Bristol-Myers Squibb Full timePosition OverviewBristol Myers Squibb is on the lookout for a dedicated Lead for Quality Control Microbiology within our Cell Therapy Facility. This pivotal role will oversee the daily operations of the QC Microbiology team, ensuring rigorous environmental monitoring and microbiological testing for both clinical and commercial cell therapy products.Key...
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Devens, United States Actalent Full timeGreat opportunity to get your foot in the door with one of the top Cell Therapy companies in the Devens, MA area! If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com Description: QA Specialist Incoming Material Disposition Onsite role Devens site Work Schedule: Monday - Friday Business Hours PURPOSE AND...
Associate Process Engineer, Cell Therapy
1 month ago
Working with UsChallenging. 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 SummaryThe Associate Process Engineer provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process. The Associate Process Engineer works closely with the Manufacturing and Quality teams to determine immediate corrective actions for deviations, identifies root cause, and implements long-term preventive actions. Other responsibilities include participation in process tech transfer, supports incoming process changes by communicating the changes to applicable departments, and participates in process improvement projects at the site. The process engineer works to identify and drive continuous improvements to the manufacturing process.Key ResponsibilitiesProvides on-the-floor and on-site troubleshooting and technical support to ManufacturingFacilitates deviation prevention and deviation closure through site quality systemsAnalyze and summarize manufacturing data to support impact assessments and investigationsOwner of change controls for routine process and procedure changesCAPA owner for Manufacturing improvementsAuthor and revise manufacturing SOPs and provide technical content and direction for electronic batch recordsParticipates in technology transfer efforts for new processes and product implementationTrain and support GMP operators on new procedures, processes, and changesApplies continuous improvement tools to identify and close procedural and compliance gapsIdentify opportunities for process improvements and operational efficiencies, and lead implementation efforts.Interfaces with other functions such as Scheduling, Global MSAT, Supply Chain, Quality, and Facilities & EngineeringSupport equipment and systems validation activities, including review of equipment qualification documents, drafting user requirements, and participating on impact assessmentsAbility to perform gowning activities and enter the manufacturing plant. Exposure to strong magnetic fields is commonplace in the manufacturing areas.Qualifications & ExperienceBSc and/or MSc degree in Science or Chem/Bio EngineeringMinimum 1+ years of industry experience. cGMP and/or Cell Therapy manufacturing experience preferred.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 CareersWith 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 ProtocolBMS 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.
