Bio Process Associate - 2nd ShiftJob Location Devens, MAWorkspace On-site position (no remote or hybrid options)Target Hiring DateMarch 2025 Work AuthorizationApplicants must have the legal right to work in the United States without requiring sponsorship. Corp-to-Corp (C2C) arrangements are not accepted RequirementsDUTIES AND RESPONSIBILITIES:
Operate control systems and processes in a Biotechnology Pilot Plant as assigned.
Prepare process buffers and reagents according to established protocols.
Maintain cleanliness and organization of equipment and work areas.
Identify and report any safety, maintenance, or operational issues to management.
Provide timely updates on operational status to area management.
Follow detailed Standard Operating Procedures (SOPs) and batch records.
Ensure compliance with cGMP and safety regulations while maintaining documentation and equipment.
Record data, log activities, and monitor process performance.
Participate in ongoing training to achieve and maintain proficiency.
EDUCATION:
A high school diploma with a minimum of 5 years process operations experience, A.A.S. or B.S. degree is preferred.
QUALIFICATIONS:
Prior job-related experience required along with demonstrated mechanical aptitude.
Familiarity with general chemistry, mathematics, microbiology and cGMP clean room operations is a plus.
Keen attention to detail.
Prior experience following and documenting written instructions is required.
Committed team player prepared to work in and embrace a team-based culture.
Shift work and overtime required.
WORKING CONDITIONS:
Shift: 5pm- 5am
Shift rotation: 3 days on (Sat, Sun, Mon), 2 days off (Tues, Wed), 2 days on (Thurs, Fri), 3 days off (Sat to Mon).
This role may involve working in an office, laboratory, or manufacturing area.
Must be able to work in gowning attire within a controlled environment for extended periods.
Must demonstrate the ability to work safely with hazardous, radioactive, and biological materials and waste, ensuring safety both when working independently and with others.
Must be able to lift up to 15 pounds as needed.
About the RoleThe role involves working in a cGMP laboratory and/or manufacturing environment, requiring strict adherence to protocols and maintaining a high attention to detail. Responsibilities include operating control systems and processes in a Biotechnology Pilot Plant, preparing process buffers and reagents, and ensuring compliance with safety and regulatory standards. The individual must properly use Personal Protective Equipment (PPE), follow aseptic processing techniques, and handle chemicals safely. Maintaining a clean and organized workspace, following detailed SOPs and batch records, and effectively communicating operational status to management are essential aspects of the job.Additionally, workers must be physically and mentally fit to perform job duties. Those operating vehicles, machinery, or working in laboratories, research, drug development, or manufacturing facilities must remain free from alcohol or illicit substances while on duty. Ongoing training and proficiency development are expected to maintain high operational standards.Apply Now (https://forms.monday.com/forms/3cdf5bfb73703e4a3aa29c55653510f4?r=use1) About the CompanyJoin Sokol GxP Services – Where Innovation Meets Integrity!Join Sokol GxP Services, where we partner with leading pharmaceutical and biotech companies to provide exceptional Commissioning, Qualification, and Validation (CQV) services. We are committed to fostering diversity, empowering local talent, and building strong community connections to bring the best-qualified candidates to our clients in the Summit, NJ area. Our inclusive and collaborative culture promotes growth and innovation, offering competitive health benefits, PTO, holiday pay, volunteer hours, a relocation budget, a 401K program, and professional development opportunities. Plus, take advantage of our Employee Referral program! Be part of a dynamic team with fantastic opportunities for growth and professional development!Let’s shape the future of life sciences together!All applicants will receive an acknowledgement that their application has been received within 2-3 weeks from the from the date of receipt.Equal Opportunity Employer Statement:Sokol GxP Services is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.Relocation support will be determined on a case-by-case basis.Our 401K program is set to launch in the 2025 fiscal year.By submitting your application and resume, you consent to have your information retained in our repository for six months. This allows us to consider you for future opportunities that may align more closely with your skills and qualifications. If a suitable position becomes available, we will contact you directly.Apply Now (https://forms.monday.com/forms/3cdf5bfb73703e4a3aa29c55653510f4?r=use1)