Bio Process Associate - 2nd Shift

SOKOL GxP Services is seeking a Bioprocess Manufacturing Associate to support hands-on production activities in a GMP-regulated biopharmaceutical manufacturing facility. This is a junior-level opportunity for candidates with manufacturing experience who are comfortable working with production equipment, electronic systems, and established operating procedures.

Key responsibilities:

• Perform routine manufacturing operations according to SOPs and written procedures.
• Weigh and verify raw materials; assemble, clean, and sterilize process equipment.
• Monitor production processes and identify deviations from established procedures.
• Complete electronic work instructions and maintain accurate manufacturing documentation.
• Maintain cleanroom conditions and follow GMP and safety requirements.
• Train on bioreactors, media and buffer preparation equipment, and manufacturing automation systems.
• Support inventory management and process documentation updates.
• Collaborate with Manufacturing, Quality, Materials Management, and Maintenance teams.
• Position details: Hourly rate: $35.60–$37.60, including shift differential; Contract length: 3 months with possible extension; Location: Devens, MA 01434; Work arrangement: 100% onsite; Shift: 5:00 PM–5:00 AM, rotating 3-2-2-3 schedule; Maximum hours: 40 hours per week; W-2 contract position; No C2C options; No visa sponsorship.

Requirements

• Required: High school diploma or equivalent; Experience in manufacturing operations; Experience working in a cGMP-regulated environment; Hands-on experience using hand tools; Proficiency with computers, including word processing, spreadsheets, and web-based applications; Ability to follow SOPs, maintain accurate documentation, and recognize deviations; Strong attention to detail, accountability, teamwork, and communication skills; Ability to work onsite in Devens, MA, on the specified rotating overnight schedule; Authorization to work in the United States without visa sponsorship.
• Preferred: Bachelor's degree in Science, Engineering, Biochemistry, or a related discipline; Experience with biopharmaceutical manufacturing equipment, including bioreactors or media and buffer preparation systems; Familiarity with DeltaV, Syncade, or OSI/PI Historian; Familiarity with SAP, Vault, or Maximo; Experience working in cleanroom environments.