cGMP Bioprocess Buffer Prep Associate — Night Shift

Randstad USA; Portsmouth (NH); On-site; USD 74,501,000 - 82,954,000; Full time

Job summary

Randstad USA seeks an entry-level Manufacturing Biotechnologist 1 in Portsmouth, NH to join a fast-paced production team. This on-site role offers hands-on cGMP experience in therapeutic protein manufacturing while working a rotating night shift.

Responsibilities include setting up and operating production equipment, basic analytical tasks, and documenting results in GDP-compliant records. This contract position provides exposure to cGMP environments and a path to growth.

Qualifications

• High School Diploma or equivalent.
• 1 to 4 years of experience in manufacturing, laboratory, or biotech production environments.
• Strict adherence to cGMP regulations and safety standards.
• Ability to work a rotating 12-hour night shift (6:30 PM - 6:30 AM; alternating weeks: Mon/Tue/Fri/Sat/Sun and Wed/Thu).

Responsibilities

• Set up, operate, and monitor production equipment, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.
• Execute process recipes primarily in the Buffer Prep area, working with Concentrates and P11 handling.
• Perform basic analytical laboratory tasks, including pH testing, conductivity monitoring, and product sampling.
• Complete written and electronic documentation adhering to strict cGMP and Good Documentation Practices (GDP).
• Execute routine facility sanitization, cleaning tasks, and raw material transfers across production areas.
• Participate in daily shift exchanges, team meetings, and continuous improvement projects.

Skills

GMP

Education

Associate

Degree in Biology, Chemistry, Life Sciences, or related field

Job description

Randstad USA seeks an entry-level Manufacturing Biotechnologist 1 in Portsmouth, NH to join a fast-paced production team. This on-site role offers hands-on cGMP experience in therapeutic protein manufacturing while working a rotating night shift.

Responsibilities include setting up and operating production equipment, basic analytical tasks, and documenting results in GDP-compliant records. This contract position provides exposure to cGMP environments and a path to growth.