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Pharmaceutical Manufacturing Associate

  • Pharmaceutical Manufacturing Associate job type Posted on: Nov 02, 2026
  • Pharmaceutical Manufacturing Associate experience level NCC Talent Solutions, LLC
  • Pharmaceutical Manufacturing Associate employment type San Diego, California
  • Pharmaceutical Manufacturing Associate salary Salary: $20 per hour
  • Pharmaceutical Manufacturing Associate employment type Onsite
  • Pharmaceutical Manufacturing Associate salary Full-time

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Job Title :

Pharmaceutical Manufacturing Associate

Job Type :

Full-Time

Job Location :

San Diego California United States

Remote :

No

Jobcon Logo Job Description :

Manufacturing Associate / Technician Location: Onsite – San Diego, CARelocation assistance is not provided for this role. Candidates must be able to work from the listed location without relocation support.Type: Full-Time - Direct HireIndustry: Pharmaceutical / Biotech (GMP)Compensation: $20 - $30 an hourRole 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 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.How you will make an impact:Execute batch production records and follow all SOPs for sterile manufacturing operationsPerform aseptic fill & finish activities in a GMP cleanroom environmentOperate and maintain filling and production equipmentPerform filter integrity testing and in-process checksConduct visual inspection of filled vials for quality and compliancePerform environmental monitoring (viable and non-viable)Support stocking and inventory of cleanroom and production suppliesAssist with cleanroom and equipment validation activitiesAccurately complete all GMP documentation and batch recordsParticipate in media fills and aseptic process qualificationsAssist in drafting and updating SOPs and Master Batch RecordsProvide input for CAPA investigations related to deviations, sterility failures, and non-conforming materialsThe experience you will bring: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 gowningStrong ability to read, interpret, and execute batch records and SOPsAbility to interpret technical instructions, including diagrams and proceduresAbility to lift up to 50 poundsAbility 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

Jobcon Logo Position Details

Posted:

Nov 02, 2026

Reference Number:

10440_4485158773

Employment:

Full-time

Salary:

$20 per hour

City:

San Diego

Job Origin:

APPCAST_CPC

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Manufacturing Associate / Technician Location: Onsite – San Diego, CARelocation assistance is not provided for this role. Candidates must be able to work from the listed location without relocation support.Type: Full-Time - Direct HireIndustry: Pharmaceutical / Biotech (GMP)Compensation: $20 - $30 an hourRole 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 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.How you will make an impact:Execute batch production records and follow all SOPs for sterile manufacturing operationsPerform aseptic fill & finish activities in a GMP cleanroom environmentOperate and maintain filling and production equipmentPerform filter integrity testing and in-process checksConduct visual inspection of filled vials for quality and compliancePerform environmental monitoring (viable and non-viable)Support stocking and inventory of cleanroom and production suppliesAssist with cleanroom and equipment validation activitiesAccurately complete all GMP documentation and batch recordsParticipate in media fills and aseptic process qualificationsAssist in drafting and updating SOPs and Master Batch RecordsProvide input for CAPA investigations related to deviations, sterility failures, and non-conforming materialsThe experience you will bring: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 gowningStrong ability to read, interpret, and execute batch records and SOPsAbility to interpret technical instructions, including diagrams and proceduresAbility to lift up to 50 poundsAbility 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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