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Manufacturing Associate

Job in San Diego, San Diego County, California, 92189, USA
Listing for: NCC Talent Solutions, LLC
Full Time position
Listed on 2026-02-18
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer, Manufacturing Production, Operations Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

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 Overview

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 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
The experience you will bring
  • 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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Position Requirements
10+ Years work experience
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