Manager, Quality Engineering in Devens, MA

Bristol-Myers SquibbDevens, MA
72d$105,450 - $127,782Hybrid

About The Position

The Manager, Quality Engineering at the Cell Therapy Facility (CTF) in Devens, MA will be responsible for providing Quality oversight of qualification and validation activities and change control for the startup and continuing operations of the Devens Cell Therapy Facility, including commissioning, qualification, and validation (CQV), computer systems validation (CSV) and process validation per established local and global standards. Bristol Myers Squibb is reimagining the future of cell therapy, leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure.

Requirements

  • Knowledge of science generally attained through studies resulting in a bachelor's degree in a scientific or engineering discipline or its equivalent.
  • A minimum of 6 years' experience in an environment governed by cGMPs, including at least 3 years of validation-related experience.

Nice To Haves

  • Knowledge of regulatory requirements, primarily cGMP, GxP, including 21CFR part 11, and good documentation practices.
  • Knowledge of applicable business systems including SAP, LIMS, Maximo and Veeva Vault.
  • Knowledge of manufacturing executions systems such as Syncade and distributive control systems such as DeltaV.

Responsibilities

  • Review and approve commissioning and qualification lifecycle documentation associated with manufacturing site facilities/equipment/and utilities.
  • Review and approve computer systems validation lifecycle documentation associated with manufacturing site, standalone and site based computerized systems.
  • Participate in and review/approve risk assessments, data integrity assessments, and technical reports supporting qualification.
  • Perform routine quality review/approval activities associated with equipment/system onboarding and status.
  • Identify improvement opportunities and support execution of team continuous improvement goals and projects.
  • Review and approve or provide impact assessment for site change controls.
  • Support internal and external inspections as required.
  • Maintain compliance with assigned learning plan.
  • Support integration of newer team members.
  • Lead meetings and represent function at cross functional meetings.

Benefits

  • Medical, pharmacy, dental and vision care.
  • Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP).
  • Financial well-being resources and a 401(K).
  • Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance.
  • Work-life programs including paid national holidays and optional holidays, Global Shutdown Days, up to 120 hours of paid vacation, and sick time off.
  • Parental, caregiver, bereavement, and military leave.
  • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits.
  • Tuition reimbursement and a recognition program.

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What This Job Offers

Job Type

Full-time

Career Level

Manager

Industry

Chemical Manufacturing

Education Level

Bachelor's degree

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