Manufacturing Associate
Listed on 2026-02-18
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Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer, Manufacturing Production, Operations Engineer
Relocation assistance is not provided for this role. Candidates must be able to work from the listed location without relocation support.
Type: Full-Time
Industry: Pharmaceutical / Biotech (GMP)
Role OverviewNCC 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 Technicians and Associates (level based on experience) to support sterile drug product manufacturing within a GMP-regulated cleanroom environment.
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.
This is an excellent opportunity for a technician who has prior experience in an aseptic processing facility.
How you will make an impact- 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
- Bachelor’s degree in Life Science. 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
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