Pharmaceutical Manufacturing Associate
Job Description
Manufacturing Associate / Technician
\n
Location: Onsite – San Diego, CA
\n
Relocation assistance is not provided for this role. Candidates must be able to work from the listed location without relocation support.
\n
Type: Full-Time - Direct Hire
\n
Industry: Pharmaceutical / Biotech (GMP)
\n
Compensation: $20 - $30 an hour
\n
\n
Role Overview
\n
NCC Talent Solutions is partnering with a Contract Manufacturing Organization in San Diego to scale up their manufacturing team to support a growing GMP operation. We are seeking multiple Manufacturing Associates (level based on experience) to support sterile drug product manufacturing within a GMP-regulated cleanroom environment.
\n
\n
This role is responsible for executing aseptic fill & finish operations, supporting cleanroom maintenance, and ensuring all production activities meet the highest standards of quality and compliance.
\n
\n
How you will make an impact:
\n
- \n
- Execute batch production records and follow all SOPs for sterile manufacturing operations
- Perform aseptic fill & finish activities in a GMP cleanroom environment
- Operate and maintain filling and production equipment
- Perform filter integrity testing and in-process checks
- Conduct visual inspection of filled vials for quality and compliance
- Perform environmental monitoring (viable and non-viable)
- Support stocking and inventory of cleanroom and production supplies
- Assist with cleanroom and equipment validation activities
- Accurately complete all GMP documentation and batch records
- Participate in media fills and aseptic process qualifications
- Assist in drafting and updating SOPs and Master Batch Records
- Provide input for CAPA investigations related to deviations, sterility failures, and non-conforming materials
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
The experience you will bring:
\n
- \n
- Bachelor’s degree in Life Science highly preferred. Experience will be considered in lieu of education.
- Typically requires 3–7+ years of experience in GMP-regulated pharmaceutical or biotech environments with experience executing activities in an aseptic manufacturing environments. Experience in drug product/drug substance manufacturing preferred.
- Hands-on experience with aseptic processing and cleanroom gowning
- Strong ability to read, interpret, and execute batch records and SOPs
- Ability to interpret technical instructions, including diagrams and procedures
- Ability to lift up to 50 pounds
- Ability to wear cleanroom PPE and gowning (including goggles, face shields, respirators, gloves) for extended periods (up to 4 hours at a time)
- Comfortable working in a controlled cleanroom environment for the majority of the workday
\n
\n
\n
\n
\n
\n
\n
\n