Execute support for various lab operations activities inclusive of equipment on biotech manufacturing in accordance with GMP-compliant procedures.
Adhere to safety protocols and ensure all work is performed in alignment with SOPs, PM work orders, and lab manuals.
Conduct routine inspections to ensure the lab meets all safety procedures.
Assist in the commissioning lab equipment and validating that it meets safety protocols.
Participate in an on-call rotation to provide timely support for the team.
Provide mentorship to entry-level technicians and collaborate with staff on complex troubleshooting.
Use the management system to ensure everything is validated, commissioned, and closed out in time.
GMP, equipment validation, inventory control, vendor management, pharmaceutical industry, Lab equipment, Data entry
GMP, equipment validation, inventory control, vendor management, pharmaceutical industry
High school diploma required.
Associate's degree in a life science preferred.
2–5 years of experience in operations in a biotech, pharmaceutical, or regulated manufacturing environment.
Minimum 1 year of experience in a cGMP setting.
Familiarity with cleanroom operations, aseptic practices, and biotech-specific systems.
Intermediate Level
The pay range for this position is $69200.00 - $84700.00/yr.
Candidates will be eligible for Avecia company benefits
This is a fully onsite position in Milford,MA.
This position is anticipated to close on Sep 12, 2025.