Manufacturing Bioprocess Specialist

Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

This a rotating 12hr position Upstream (05:00PM-05:00AM)

Works on routine manufacturing assignments per written procedures that are complex with on instructions, where ability to recognize deviation from accepted practice is required.2. Adheres to Good Manufacturing Practices and standard operating procedures.3. Weighs and checks raw materials. Assembles, cleans and sterilizes process equipment, monitors processes.4. Completes electronic work instructions and maintains clean room environment to comply with regulatory requirements.5. Operates 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.)6. 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.).7. Ensures less experienced manufacturing personnel comply with Standard Operating Procedures (SOPs) and electronic work instructions.8. Assists with the coordination and implementation of special projects such as validation or complex investigations.9. Revises and creates process documents with no instructions, supports routine process investigations. 10. Assists with reviewing batch and exception reports for each manufacturing lot in conjunction with Quality representative. 11. Champions areas specific initiatives associated with work safety12. Engages in and supports culture of continual improvement through ownership of improvement for work processes, equipment and safe work environment.

Required:

Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry or related discipline, or its equivalent is desired but not required.

A minimum of 5 years process operations experience in a highly automated biotechnology manufacturing facility subject to Good Manufacturing Practices (GMP) regulations.

Strong knowledge of either upstream and/or downstream unit operation is essential.

Practical knowledge of regulations such as GMP and company Standard Operating Procedures (SOP).

Prior evidence of successful participation on work teams where combined contribution, collaboration, and results were expected

Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web based applications.

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 the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Company info

Bristol-Myers Squibb Company
Website : http://www.bms.com