Bristol Myers Squibb
pharmaceutical
AssociateSpecialistManufacturingProcessExcellence
“Associate Specialist Manufacturing Process Excellence at Bristol Myers Squibb. Skills: Manufacturing process excellence, Technical documentation, Equipment qualification, Continuous improvement. Supports manufacturing process documentation, equipment commissioning and troubleshooting, and continuous improvement initiatives. Writing technical documentation”
What You'll Achieve.
Ensuring timely closure of quality records; Ensure on-time closure of quality records
Industry & Context.
Troubleshooting; A3 problem solving initiatives; Investigation; CAPAs
What They're Looking For.
Must Have
Bachelor’s degree or equivalent in technical discipline, 0–2 years of experience in pharmaceutical operations, Understanding of GMP and technical processes, Proficiency in French (mandatory), Proficiency in English
What You'll Do.
Supports manufacturing process documentation, equipment commissioning and troubleshooting, and continuous improvement initiatives, Writing technical documentation, Participating in equipment qualification activities, Ensuring timely closure of quality records, Provide Expertise in manufacturing processes, Write technical documentation, Participate in the Commissioning, FAT/SAT, IOQ, PQ and Operational Readiness as part of new equipment, Write System requirement definition & associated supporting quality records and documentation (e.g.
change management, …) to support equipment enhancement post product commercialization or Manufacturing process, Support Data Integrity risk assessment, Prepare and assist Operations teams with new equipment set up and troubleshooting, Participate in equipment qualification tasks, Deploy, maintain & execute level 1 maintenance, Act as primary point of contact for equipment troubleshooting, Write LO/TO documentation (e.g ECP), Participate in A3 problem solving initiatives related to technical topics, Own & lead local continuous improvement initiatives, Provides technical expertise for investigation, CAPAs, Process improvement and in other various topics upon request, Ensure on-time closure of quality records (e.g.
CAPA, Action, document periodic review,.
), Own and lead change control at the discretion of the production team.
How You'll Work.
Team & Collaboration
Working alongside high-achieving teams; Assist Operations teams with new equipment set up and troubleshooting; Participate in A3 problem solving initiatives related to technical topics; Provides technical expertise for investigation, CAPAs, Process improvement and in other various topics upon request
Communication Scope
Proficiency in French (mandatory); Proficiency in English
Process & Methodology
Own & lead local continuous improvement initiatives, Own and lead change control at the discretion of the production team
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