Manufacturing Associate

TekWissen is a global workforce management provider offering strategic talent solutions to clients worldwide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence to deliver innovative medicines for a wide range of diseases.

About the role

The Manufacturing Services Associate I supports all cGMP manufacturing production suites by ensuring suites are stocked with raw materials and consumables, assembling and autoclaving components, cleaning soiled parts, maintaining analytical equipment, and completing scheduled cleaning tasks. This role requires a basic understanding of cGMP compliance, aseptic technique, and cross-contamination awareness.

Responsibilities

• Perform 6S activities and stock each suite daily.
• Clean soiled parts daily.
• Determine production needs for autoclaved assemblies and deliver them to production suites.
• Perform daily and weekly maintenance activities on analytical equipment.
• Perform weekly and monthly cleaning of inoculum rooms.
• Report all activities in written and electronic documents in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs).
• Attain qualification for all assigned tasks and maintain an individual training plan.
• Prepare materials for transport and delivery to manufacturing suites.
• Perform material movements into, out of, and across production areas.
• Maintain facility and equipment through routine cleaning and sanitization.
• Perform administrative tasks, including attending suite shift exchanges, meetings, sending and receiving emails, and participating in projects.
• Adhere to cGMPs at all times during the manufacture of APIs.
• Own the quality of work delivered and notify management of regulatory inspections, GMP deficiencies, process deviations, or product defects.
• Follow job safety procedures, attend health and safety training, and comply with company and site safety policies.
• Perform other duties as assigned.

Requirements

• High School Diploma or equivalent (required).
• Associate's or Bachelor's degree in a science-related discipline (preferred).
• Basic understanding of cGMP compliance.
• Ability to demonstrate aseptic technique and cross-contamination awareness.
• Strong written and verbal communication skills.
• Mechanically inclined with the ability to assemble parts following provided procedures.
• Flexibility to adapt to changing business priorities.
• Open to performance feedback and translates it into action.

Schedule

12-hour shift from 07:00 AM to 07:00 PM, alternating between Monday, Tuesday, Friday, Saturday, Sunday, and Wednesday/Thursday.

Location: Portsmouth, NH 03801
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite