Bristol Myers Squibb Associate Engineer in Devens, Massachusetts

Title: Associate Engineer

Location: NA-US-MA-Devens

Job Number: 1702269

At Bristol-Myers Squibb, we believe that together we can make the difference. We want to do this by building professional teams who can create and innovate medicines that benefit doctors and their patients.

Our large-scale biologics manufacturing facility in Devens, Massachusetts, is expanding and there are a number of exciting career opportunities to join Bristol-Myers Squibb, one of the world’s leading BioPharma companies.

We’ve created one of the world’s premier biologics facilities, among the first sites in the industry to have a fully automated, integrated manufacturing control system that enables the plant to run virtually paperless. It is a site that combines biologics development with clinical and commercial manufacturing on a single campus – a true biologics center of excellence for the company where teams are encouraged to closely collaborate. This expansion was designed to support the launch of new medicines by more closely aligning biologics development and manufacturing capabilities. All this goes towards helping create and innovate life-saving medicines that fight serious illnesses.

Reporting to the Manager of Upstream Devens Manufacturing Technology, the Associate Engineer, Manufacturing Technology is to serve as a process technical expert to large scale cell culture and harvest unit operations for the commercial manufacture of biopharmaceuticals at Devens. This position offers the opportunity to provide highly visible technical leadership to resolve complex problems while meeting quality, schedule, and cost objectives. The successful candidate will be a key contributor in a dynamic and highly collaborative team environment. The candidate will set appropriate objectives and priorities, overcome obstacles; and deliver results within project timelines. Expertise and experience in the design, control, and operation of large scale inocula, seed train, bioreactor, filtration and centrifugation unit operations are highly desired. Demonstrated skills in cross-functional partnerships, supporting crossfunctional teams and knowledge of regulatory and cGMP requirements are required.

Responsibilities:

  • May act as upstream lead, Manufacturing Technology during absence of Senior Engineer, Upstream.

  • Provides technical expertise for investigation and resolution of process deviations, root cause investigation, CAPAs,

process improvements, review and approval of change controls.

  • Supports commercial manufacturing via in-plant coverage and real-time process upset troubleshooting.

  • Evaluates process performance through statistical analysis with recommendations generated for process enhancement.

  • Liaises with network technical product team sub-functions as Devens site representative.

  • Supports upstream aspects of process technology transfer and process validation through individual technical contribution.

  • Supports the preparation of CMC documentation for regulatory filings and responses for the BMS-Devens commercial manufacturing facility.

  • Provides interface as supporting process subject matter expert during regulatory inspections.

Qualifications:

  • BS in the biological sciences or chemical/biochemical engineering, a related discipline, or its equivalent.

  • BS or equivalent with 2-4 years relevant experience, MS or equivalent with 0-2 years relevant experience.

  • Proficiency of SOPs, cGMPs and the know how to work and manage within a regulatory environment.

  • Experience in successful execution and management of process technical transfer.

  • Experience in designing and executing process and equipment validation plans.

  • Experience in the design, modification and optimization of biologics cell culture unit operations.

  • Experience in investigating process deviations and developing issue resolving CAPAs.

  • Proven project management skills and effectively balancing project assignments with other duties.

  • Experience with biopharmaceutical regulatory submissions and interaction with regulatory agency inspectors.

  • Excellent verbal & written communications skills.

  • Interpersonal and facilitation skills necessary to interface with and influence all levels of the organization with the ability to lead people and multi-disciplinary teams.

  • Principal assignment is in a modern LSCC building which requires adherence to various Personal Protective Equipment (PPE) standards.

Together, we make a difference. Bristol-Myers Squibb is one of the world’s BioPharma leaders, committed to delivering innovative medicines as well as nurturing a culture that’s a springboard for progress. Our success depends on building teams of bold, innovative and passionate employees who will help continue to drive us further forward. No matter the role, we are united by our mission and determined to win this fight. And that makes all the difference. If you want to join us, apply now at www.bms.com/careers .

Bristol-Myers Squibb is an equal opportunity employer - Minorities/Females/Protected Veterans/Disabled

Job: Process