Senior Manufacturing Bioprocess Associate

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.

Duties/Responsibilities:


Operates control systems and processes supporting biologics process manufacturing.

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

Maintains files, records data, logs activities, and monitors processes.

Prepares process buffers, media and reagents.

Cleans and Steam sterilizes equipment and maintains area in a clean and orderly fashion to support the manufacturing schedule.

Recognizes and reports safety, maintenance and quality events to area management.

Communicates status of operations to area management in a timely manner.

Achieves and maintains proficiency through training.

Assists with reviewing batch and exception reports for each manufacturing lot in conjunction with Quality representative.


Engages in and supports culture of continual improvement through ownership of improvement for work processes, equipment and safe work environment

QUALIFICATIONS

Specific Knowledge, Skills, Abilities, etc:


Prior job related experience required along with demonstrated mechanical aptitude and high level of attention to detail.

Prior process operations experience in a biotechnology manufacturing facility or related industry subject to current Good Manufacturing Practices (cGMP) regulations.

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

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

Familiarity with general chemistry, mathematics, microbiology and cGMP operations is desirable.

Work/study experience where attention to detail, adherence to written instruction, and personal accountability were critical to success

Demonstrated successful participation on work teams where combined contribution, collaboration, and results were expected

Demonstrates good interpersonal skills, is attentive and approachable with the ability to embrace a team based culture.

Demonstrated ability to communicate expectations and results to the operating staff and management as needed to maintain production timelines and organizational goals.


Education/Experience/ Licenses/Certifications:

The successful candidate will have a high school diploma. 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 3 years process operations experience in a biotechnology manufacturing facility subject to current Good Manufacturing Practices (cGMP) regulations.

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

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