Site Location: NH
Position reports to: Manufacturing
Pay: $20-30/hour based on experience. There are 3 levels of Manufacturing Technicians.
We are hiring pharmaceutical Manufacturing Associates in the Northern Mass/Southern NH area. You would join the Global Manufacturing and Supply Department and be part of a high caliber team that takes pride in helping provide life saving medicines to patients world-wide.
As a Manufacturing Associate, you will perform and document daily manufacturing operations according to SOPs in a cGMP environment, operate biologics production equipment (bioreactors, filtration units, chromatography systems and fixed/portable vessels), and execute validation protocols.
This position will report to a Manufacturing Supervisor. There are a variety of shifts available, Full time work only.
The Manufacturing Associate will support the production of therapeutic proteins under current Good Manufacturing Practices (cGMP) conditions. This role involves executing process recipes, following Standard Operating Procedures (SOPs), monitoring equipment, and performing laboratory tasks such as pH and conductivity testing, product sampling, and routine sanitization. Associates work under supervision while demonstrating a strong understanding of cGMP compliance and aseptic techniques.
• Set up and operate equipment, monitor production processes (e.g., clean-in-place (CIP) and steam-in-place (SIP)), and report production in written and electronic formats in accordance with Good Documentation Practices (GDPs).
• Troubleshoot equipment issues and review documentation as necessary.
• Attain qualification for assigned tasks and maintain an individual training plan.
• Perform laboratory tasks such as monitoring pH, conductivity, and product sampling.
• Support facility cleanliness by performing routine sanitization and participating in 6S programs.
• Assist with material movement and transfer of materials and chemicals within production areas.
• Participate in administrative tasks, including shift exchanges, meetings, and project involvement.
• Support data integrity by following policies, guidelines, and procedures and identifying issues to management.
• High school diploma or GED required.
• Experience in GMP environment desirable.
• Ability to perform basic computer operations, such as ability to navigate in MS Office, use email, and complete training using Web Based Training (WBT).
• Must be Greencard holder or a US Citizen.
