Shift Technician, Sterile Drug Product MaintenanceThe role involves working within the Drug Product Maintenance team to support the safe, reliable operation of equipment used in vial and syringe filling and inspection.Key Duties and ResponsibilitiesWork with the project & CQV team to facilitate delivery, validation, and safe operation of equipment related to vial/syringe filling and inspection.Ensure all maintenance and calibration activities comply with regulatory requirements, quality systems (cGDP/GMP), EHS, and local engineering procedures.Interpret P&IDs, equipment layouts, wiring diagrams, and specifications to plan and perform maintenance and repairs.Use knowledge of sterile fill/finish process equipment to support manufacturing, quality, automation, validation, and EHS for deviation investigation, change control, and CAPA activities.Manage CMMS work requests and work orders, including generation, processing, tracking and follow‑up to ensure timely completion.Assist in advanced troubleshooting and repair of equipment and systems, including diagnosis of automation and controls.Respond promptly to equipment failures or issues, providing guidance and prevention actions.Execute planned maintenance routines—predictive, preventive, and calibration activities.Understand and implement HSA and safety requirements for maintenance operations.Collaborate with manufacturing operations, planners, and EHS to align maintenance with production planning.Support the quality team in timely handling of deviations, change controls, and CAPAs.Work with the EHS team to ensure safety investigations and CAPAs are closed on time.Assist the Maintenance Manager in long‑term production planning and site metrics, ensuring major maintenance outages are scheduled.Champion a safety culture within the maintenance team.Provide additional maintenance support as needed, including training material development, vendor management and continuous improvement activities.Required QualificationsMulti‑skilled professional with a craft qualification in Electrical, Instrument, or a combined trade.Experience with site start‑up and handover from CQV to sustaining operations.Experience in a regulated biopharmaceutical, pharmaceutical, medical device, facilities maintenance or FMCG facility.Proven ability to prioritize maintenance activities to achieve a safe and reliable site.Experience operating and fault‑finding PLC‑based control systems.Demonstrated ability to influence cross‑functional work in a matrix environment during startup and commercial manufacture.Excellent communication skills and ability to work as part of a multi‑disciplined, cross‑functional team.High attention to detail, strict adherence to procedures, and flexibility to adapt to change.Experience maintaining complex equipment in a fast‑paced environment.Demonstrated experience effectively managing stakeholders.Desired QualificationsBachelor’s degree in Engineering, Automation or equivalent experience in utilities or process controls, automation and/or information systems within the biotechnology or pharmaceutical industry.Maintenance experience in sterile fill/finish.BenefitsCompetitive salary and annual bonusPension contributionFamily medical allowance27 days annual leaveLife assuranceOn‑site gymEEO StatementVisit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.Candidate RightsCandidate Rights: BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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