Downstream Senior Bioprocess Associate

Job Overview The Bioprocess Associate/Specialist assists in the execution of manufacturing processes according to established work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs). Shift: B2 rotating shift 6:00PM–6:30AM. Major Duties and Responsibilities Works on routine manufacturing assignments per written procedures that are moderately complex with minimal instructions, where ability to recognize deviation from accepted practice is required. 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 primary production equipment within assigned functional area (e.g., bioreactors, chromatography skids, media or buffer preparation equipment). Uses in‑process automation systems (DeltaV, Syncade Interactions, Pi Vision) and supporting business systems (SAP, Infinity, Maximo) to maintain production records. Revises and creates process documents with little to no instruction; assists with process‑related investigations. Helps maintain material and component inventory levels. Assists with reviewing batch and exception reports associated with each manufacturing lot, in conjunction with supervisor and quality representative. Assists with area‑specific initiatives related to work safety. Knowledge and Skills High school diploma required. Knowledge of science, engineering, biochemistry or related discipline desirable but not required. Minimum 2+ years of process operations experience in a highly automated biotechnology manufacturing facility subject to Good Manufacturing Practices (GMP) regulations. Practical knowledge of regulations such as GMP and company SOPs. Evidence of successful participation on work teams with collaboration and results. Proficiency in common computer tools: word processing, spreadsheets, web‑based applications. Attention to detail and personal accountability critical to success. Good interpersonal skills; attentive and approachable. Maintains a professional and productive relationship with area management and co‑workers. Working Conditions Work performed in a state‑of‑the‑art large‑scale cell culture facility with classified areas requiring appropriate personal protective equipment (PPE). Roles may involve contact with hazardous materials such as caustic chemicals and steam. Compensation Overview Location: Devens, MA – $29.83 – $36.15 per hour for a full‑time employee. Additional incentive cash and stock opportunities may be available based on eligibility. Benefits Health coverage: medical, pharmacy, dental, and vision care. Well‑being support: BMS Well‑Being Account, BMS Living Life Better, Employee Assistance Programs (EAP). Financial security: 401(k) plan, disability insurance, life and accident insurance. Work‑life benefits: paid time off, flexible time off, unlimited paid sick time (where applicable). Equal Employment Opportunity Visit for our Equal Employment Opportunity statement. Data Protection We will never request payments, financial information, or social security numbers during the application or recruitment process. Learn more at #J-18808-Ljbffr Bristol-Myers Squibb