Bio Process Associate - 2nd Shift
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Before you apply
Salary$36 – $38/hr
LocationDevens, Massachusetts, United States
Work modeon-site
Typecontract
SeniorityEntry
DepartmentManufacturing
Company size11+ people
PostedOct 20, 2026 · 2w ago
Verified live2d ago
At a glanceSummarised by Seekless from the posting.
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
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
Ability to work onsite in Devens, MA, on the specified rotating overnight schedule
Authorization to work in the United States without visa sponsorship
Skills
word processing
spreadsheets
web-based applications
DeltaV
Syncade
OSI/PI Historian
SAP
Vault
Maximo
Benefits
Health insurance
Dental insurance
Vision insurance
Holiday pay
401(k)
Employee referral bonus
Contract to hire
About the role
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.
Responsibilities
Key responsibilities:
•
Perform routine manufacturing operations according to SOPs and written procedures.
•
Weigh and verify raw materials; assemble, clean, and sterilize process equipment.
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Monitor production processes and identify deviations from established procedures.
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Complete electronic work instructions and maintain accurate manufacturing documentation.
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Maintain cleanroom conditions and follow GMP and safety requirements.
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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;
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Contract length: 3 months with possible extension;
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Location: Devens, MA 01434;
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Work arrangement: 100% onsite;
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Shift: 5:00 PM–5:00 AM, rotating 3-2-2-3 schedule;
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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:
Nice to have
•
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.
Benefits
•
Health insurance with dental and vision insurance options.
•
Holiday pay.
•
401(k) program.
•
Employee referral bonus program.
•
The client retains the right to hire the contractor directly.