Bio Process Associate - 1st Shift

TSR Consulting

  • Massachusetts, MA
  • 1 day ago
  • $25–$30.68 Per Hour
  • Contractor

Highlights

Operate production equipment in assigned area, including upstream (media formulation, glass washers, dispensary, bioreactors, harvest equipment) or downstream (buffer systems, glass washers, chromatography skids, membrane operations, column packing skids). The ideal candidate will have strong experience in GMP biotechnology manufacturing, upstream and/or downstream operations, and automation systems and a proven ability to execute complex procedures, maintain compliance, and drive continuous improvement .

Numbers & Facts

LocationMassachusetts, MA
Job TypeContractor
Salary$25–$30.68 Per Hour

Description

Job Title: Bio Process Associate - 1st Shift

Location: Devens, MA

Duration: Temp - 6 months + possible extension

Pay Range: $20/hr - $30/hr (W2)

Onsite Requirement: 100% onsite

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.

About TSR

TSR is a trusted staffing and workforce solutions partner with more than 50 years of experience delivery highly qualified talent to support clients' most critical business and technology initiatives. Through a disciplined approach to sourcing, candidate vetting, and delivery, TSR helps organizations scale teams quickly while maintaining quality and reliability. TSR operates with a global delivery model, leveraging specialized teams to support enterprise clients across North America and beyond.

In June 2024, TSR was acquired by Justin Christian, founder and CEO of BCforward, a global provider of professional services and workforce solutions. This partnership expands TSR's ability to deliver broader capabilities, global delivery resources, and enhanced opportunities for both clients and consultants.

Job Description

We are seeking a Bio Process Associate - 1st Shift to join our dynamic team. The ideal candidate will have strong experience in GMP biotechnology manufacturing, upstream and/or downstream operations, and automation systems and a proven ability to execute complex procedures, maintain compliance, and drive continuous improvement.

Responsibilities:

  • Execute routine manufacturing assignments per written procedures that may be complex, recognizing and addressing deviations from accepted practices.
  • Adhere to Good Manufacturing Practices and Standard Operating Procedures.
  • Weigh and verify raw materials and document results.
  • Assemble, clean, and sterilize process equipment and monitor associated processes.
  • Complete electronic work instructions and maintain cleanroom standards to meet regulatory requirements.
  • Operate production equipment in assigned area, including upstream (media formulation, glass washers, dispensary, bioreactors, harvest equipment) or downstream (buffer systems, glass washers, chromatography skids, membrane operations, column packing skids).
  • Use process automation systems such as DeltaV, Syncade, and OSI/PI Historian, and supporting business systems such as SAP, TrackWise, and Maximo.
  • Support compliance of less experienced personnel with SOPs and electronic work instructions.
  • Assist with coordination and execution of special projects, including validation and complex investigations.
  • Revise and create process documents and support routine process investigations.
  • Assist in review of batch records and exception reports with Quality representatives.
  • Champion area-specific initiatives to promote work safety.
  • Engage in continuous improvement to enhance processes, equipment reliability, and safe working conditions.

Required Skills & Qualifications:

  • High school diploma required. Bachelor's degree in science, engineering, biochemistry, or related discipline desired or equivalent experience.
  • 1+ years of process operations experience in a highly automated GMP biotechnology manufacturing facility.
  • Strong knowledge of upstream and/or downstream unit operations.
  • Practical knowledge of GMP regulations and SOPs.
  • Demonstrated teamwork, collaboration, and results orientation.
  • Proficiency with common computer tools, including word processing, spreadsheets, and web applications.
  • Proven attention to detail and personal accountability in prior roles.
  • Effective interpersonal skills with an attentive and approachable style.
  • Ability to maintain professional and productive relationships with management and co-workers.

Preferred Skills:

  • Experience with DeltaV, Syncade, and OSI/PI Historian.
  • Experience with SAP, TrackWise, and Maximo.

Why TSR?

At TSR, we believe in advancing lives and careers. When you join our team, you gain access to:

  • Competitive compensation and benefits.
  • Opportunities for growth with global clients.
  • A supportive, inclusive culture that values innovation and people.
  • Exposure to cutting-edge technologies and projects.

About Our Commitment

TSR is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, or veteran status.

Interested? Apply Now!

If this sounds like the right opportunity for you, please apply with your most recent resume at

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