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Downstream Technical Lead (Night Shift)

Bristol Myers Squibb
Devens - MA, United States, United Statesfull_timeVerifiedPosted 3 Jan 2025

About the role

Working 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 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.

The Technical Lead is the shift's technical expert in the execution of commercial manufacturing processes according to established electronic work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs).

**This is a rotating 12hr 2nd shift position (5PM-5AM) therefore eligible for a 20% shift differential

Key Responsibilities:

  • Works on routine manufacturing assignments as well as assignments that are very complex in nature where independent action and a high degree of initiative are required in resolving problems and making recommendations. – striving for right first time through adherence of GMP activities

  • Change control identifiers – works in conjunction with bioprocess associate/specialists to identify key improvements initiatives and direct changes to project leads for initiation

  • Investigation identifiers – initiate investigation following alignment with QA floor

  • Communicate and resolve operational variances

  • Serve as the “acting” Shift Supervisor/Manager in absence of Shift Supervisor/Manager – Coordinate, direct and oversee work execution and manage personnel related issues

  • Executes real time process monitoring – including equipment and key process parameters review and work with Shift Supervisor/Manager to drive required decisions

  • Drive implementation of process enhancement and new technology in partnership with Project lead and Manufacturing Technology team

  • Participate in performance review discussion

  • Leads complex investigations on floor – drives technical issues in working with cross functional team members

  • Support real time process reports review and resolve open issues.  Trend issues and strives to right first time

  • Technical trainer for the shift – provides consistent training to the staff

  • Execute and drive continuous improvements

  • Support Tech transfer team through active participation in ensuring that new process can fit and executes in sustainable manner

  • Being resource to support routine investigations and CAPAs– author, review, approval, in case of excess investigation beyond planned capacity

  • Assigned area owner – drive facility upkeeps

  •  Adheres to Good Manufacturing Practices and standard operating procedures

  • Weighs and checks raw materials.  Assembles, cleans and sterilizes process equipment, monitors processes

  • Completes electronic work instructions and maintains clean room environment to comply with regulatory requirements

  • Operates and trains others all production equipment within the assigned functional area (i.e. Upstream: Media formulation equipment, glass washers, dispensary, bioreactors, harvest equipments or Downstream: Buffer equipment, glass washers, chromatography skids, membrane operations, column packing skids, etc.)

  • Effectively uses process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.)

  • Ensures less experienced manufacturing personnel comply with Standard Operating Procedures (SOPs) and electronic work instructions and that training is completed on time

  • Assists with the coordination and implementation of special projects such as validation or complex investigations

  • May provide scheduling and work assignment guidance to peers

  • Modifies group work plan, schedule or assignments to meet shift/unit priorities, maintains operational efficiency, m

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Company

Bristol Myers Squibb

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