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Bio Process Associate - 1st Shift

Job in Devens, Worcester County, Massachusetts, 01434, USA
Listing for: Sunrise Systems Inc
Full Time position
Listed on 2026-07-31
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Quality Engineering, Production QC/QA, Manufacturing & Industrial Operations
Job Description & How to Apply Below
Location: Devens

Job Title:
Bio-Process Associate

Location:

Devens, MA 01434 - 100% onsite
Duration: 6 Months

Work Schedule:

Shift rotation: 3 days on (Sat, Sun, Mon), 2 days off (Tues, Wed), 2 days on (Thurs, Fri), 3 days off (Sat to Mon).
Required to work on holidays and weekends as scheduled

Must Haves:

  • Strong knowledge of either upstream and/or downstream unit operation is essential.
  • 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, spreadsheets, and web-based applications.
  • Previous work experience where attention to detail and personal accountability were critical to success
Key Responsibilities:
  • Works on routine manufacturing assignments per written procedures that are complex with on 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 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.)
  • 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.).
  • Ensures less experienced manufacturing personnel comply with Standard Operating Procedures (SOPs) and electronic work instructions.
  • Assists with the coordination and implementation of special projects such as validation or complex investigations.
  • Revises and creates process documents with no instructions, supports routine process investigations.
  • Assists with reviewing batch and exception reports for each manufacturing lot in conjunction with Quality representative.
  • Champions areas specific initiatives associated with work safety.
  • Engages in and supports a culture of continual improvement through ownership of improvements to work processes, equipment, and the safe work environment.
Qualifications & Experience:
  • High school diploma is 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 1 + 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.
  • Previous work experience where attention to detail and personal accountability were critical to success
  • Demonstrates good interpersonal skills, is attentive and approachable.
  • Maintains a professional and productive relationship with area management and co-workers
Contact:
Sunny Rajput |  | URL:
Position Requirements
10+ Years work experience
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