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Junior Process Engineer, Cell Therapy
2 months ago
At Bristol Myers Squibb, we redefine what it means to work in a challenging and rewarding environment. Here, every day presents unique opportunities to engage in impactful work that changes lives.
From enhancing production processes to pioneering advancements in cell therapy, our mission is to improve patient outcomes while fostering the growth of our employees.
We believe in providing a balanced and flexible work atmosphere, offering a comprehensive range of competitive benefits and resources to help our team members achieve their professional and personal aspirations.
Position OverviewThe Junior Process Engineer plays a crucial role in supporting the manufacturing operations at our Cell Therapy Facility (CTF) within a Good Manufacturing Practice (GMP) framework.
This role involves providing technical assistance for troubleshooting process and equipment issues that arise during production. The Junior Process Engineer collaborates closely with Manufacturing and Quality teams to address immediate concerns, identify root causes, and implement sustainable corrective measures.
Additional responsibilities include participating in process technology transfers, communicating changes to relevant departments, and engaging in continuous improvement initiatives at the facility.
Key Responsibilities- Deliver on-site troubleshooting and technical support to manufacturing operations.
- Facilitate the prevention and resolution of deviations through established quality systems.
- Analyze manufacturing data to support impact assessments and investigations.
- Oversee change controls for routine process and procedural modifications.
- Act as the CAPA owner for manufacturing enhancements.
- Draft and update manufacturing Standard Operating Procedures (SOPs) and provide technical guidance for electronic batch records.
- Contribute to technology transfer efforts for new processes and product launches.
- Train and assist GMP operators on new procedures and process modifications.
- Utilize continuous improvement methodologies to identify and address procedural and compliance gaps.
- Identify and lead initiatives for process enhancements and operational efficiencies.
- Collaborate with various functions, including Scheduling, Global MSAT, Supply Chain, Quality, and Facilities & Engineering.
- Support equipment and systems validation activities, including reviewing qualification documents and drafting user requirements.
- Perform gowning activities and access the manufacturing facility, with exposure to strong magnetic fields.
A Bachelor’s or Master’s degree in Science or Chemical/Biological Engineering is required, along with a minimum of 1 year of industry experience. Experience in cGMP and/or Cell Therapy manufacturing is preferred.
If you encounter a position that interests you but does not perfectly align with your qualifications, we encourage you to consider applying.
On-site ProtocolBristol Myers Squibb has a diverse occupancy structure that dictates where employees perform their duties. This includes site-essential, site-by-design, field-based, and remote-by-design roles.
Site-essential roles necessitate 100% onsite presence, while site-by-design roles may allow for a hybrid work model with at least 50% onsite participation. Onsite presence is critical for collaboration, innovation, productivity, and fostering a positive company culture.
Bristol Myers Squibb is committed to ensuring that individuals with disabilities can thrive through a transparent recruitment process, reasonable workplace accommodations, and ongoing support.
We prioritize the health and safety of our employees and recommend that all team members stay fully vaccinated against Covid-19 and remain updated on boosters.
We are an equal opportunity employer and will consider qualified applicants with arrest and conviction records, in accordance with applicable laws.
All data processed during the application process will be handled in compliance with relevant data privacy policies and regulations.
