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Junior Process Engineer, Cell Therapy
2 months ago
At Bristol Myers Squibb, we redefine the meaning of work. Here, every day presents unique challenges that are both significant and impactful. Our environment fosters innovation, from enhancing production processes to pioneering advancements in cell therapy. You will have the opportunity to develop your career in a setting that values diversity and collaboration.
Position Overview
The Junior Process Engineer plays a crucial role in supporting the manufacturing operations at the Devens Cell Therapy Facility (CTF) within a GMP framework. This role involves providing technical assistance to address and resolve process and equipment issues that arise during production. The Junior Process Engineer collaborates closely with both Manufacturing and Quality teams to establish immediate corrective measures for any deviations, identify underlying causes, and implement sustainable preventive strategies. Additional responsibilities include participating in technology transfer processes, facilitating communication regarding incoming process modifications, and engaging in site-wide process enhancement initiatives. The engineer is tasked with recognizing and driving continuous improvements in manufacturing operations.
Key Responsibilities
- Deliver on-site troubleshooting and technical support to manufacturing teams.
- Facilitate the prevention and resolution of deviations through established quality systems.
- Analyze manufacturing data to support assessments and investigations.
- Manage change controls for routine process and procedural updates.
- Oversee CAPA initiatives aimed at manufacturing enhancements.
- Draft and update manufacturing SOPs, providing technical guidance for electronic batch records.
- Participate in technology transfer activities for new processes and product launches.
- Train and assist GMP operators in new procedures and process changes.
- Utilize continuous improvement methodologies to identify and rectify procedural and compliance deficiencies.
- Spot opportunities for operational efficiencies and lead their implementation.
- Collaborate with various functions, including Scheduling, Global MSAT, Supply Chain, Quality, and Facilities & Engineering.
- Support validation activities for equipment and systems, including reviewing qualification documents and drafting user requirements.
- Be prepared to perform gowning procedures and access the manufacturing facility, which may involve exposure to strong magnetic fields.
- BSc and/or MSc degree in Science or Chemical/Biological Engineering.
- A minimum of 1+ years of relevant industry experience, with a preference for cGMP and/or Cell Therapy manufacturing exposure.
Work Environment
Our diverse occupancy structure dictates where employees conduct their work, encompassing site-essential, site-by-design, field-based, and remote roles. The nature of your position will determine your assigned occupancy type.
Bristol Myers Squibb is committed to ensuring that individuals with disabilities can thrive through a transparent recruitment process and ongoing support in their roles.
We prioritize the health and safety of our employees and strongly recommend that all staff members stay up to date with Covid-19 vaccinations and boosters.
We are an equal opportunity employer and consider qualified applicants regardless of arrest and conviction records, in accordance with applicable laws.
