Bio Process Associate - 2nd Shift

SOKOL GxP Services; Ayer (MA); On-site; USD 49,000 - 52,000; Full time

Benefits offered by this job

Health insurance with dental andvision

Holiday pay

401(k) program

Employee referral bonus program

Job summary

SOKOL GxP Services is seeking a Bioprocess Manufacturing Associate for hands-on production in a GMP-regulated biopharmaceutical facility. This junior role targets candidates with manufacturing experience who are comfortable with production equipment, electronic systems, and SOPs.

Responsibilities include routine operations, materials handling, documentation, cleanroom duties, and training on reactors and automation systems. Onsite in Devens, MA with a rotating 5:00 PM–5:00 AM schedule.

Qualifications

• 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 (word processing, spreadsheets, web apps).
• Ability to follow SOPs, maintain documentation, and recognize deviations.
• Strong attention to detail, accountability, teamwork, and communication.
• Ability to work onsite in Devens, MA on rotating overnight schedule.
• Authorization to work in the United States without visa sponsorship.

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.

Skills

Manufacturing operations

cGMP environment

Hand tools

Computers

SOP adherence

Attention to detail

Teamwork & communication

Onsite work

Education

High school diploma or equivalent

Bachelor's degree in Science/Engineering/Biochemistry

Tools

DeltaV

Syncade

OSI/PI Historian

SAP

Vault

Maximo

Job description

• Shift: 5:00 PM–5:00 AM, rotating 3-2-2-3 schedule;

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.

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.