QA Coordinator (Contract) – GMP / Quality OperationsFrey Consulting Group • Carpinteria, California, United States
QA Coordinator (Contract) – GMP / Quality Operations
Frey Consulting Group
- Carpinteria, California, United States
- Carpinteria, California, United States
About
Shift: 2nd Shift | 3:00 PM – 11:30 PM
Duration: Contract through December 2026 (with potential extension)
Schedule: Full-Time (40 hours/week)
About the Opportunity Recruits Lab is seeking a QA Coordinator to support quality operations within a regulated manufacturing environment. This opportunity is ideal for candidates with experience in quality control, laboratory testing, pharmaceutical manufacturing, or chemical manufacturing environments.
The successful candidate will support product quality, compliance, laboratory testing, documentation, and quality system initiatives while working closely with operations and quality teams.
Key Responsibilities
Perform sampling and testing of raw materials, intermediates, and finished products
Conduct laboratory analyses and provide timely, accurate results
Support quality-related investigations and issue resolution
Maintain GMP‑compliant documentation, records, and logbooks
Assist with ISO quality system implementation and maintenance
Perform calibrations, standard preparations, and related documentation
Utilize analytical techniques including HPLC, GC, and wet chemistry methods
Record and maintain quality data within SAP and other quality systems
Support batch release timelines while ensuring quality and compliance standards are met
Participate in safety initiatives and emergency response activities
Train and support operators on quality procedures and best practices
Qualifications Required
High school diploma or equivalent
1–2 years of experience in Quality Assurance, Quality Control, or a regulated manufacturing environment
Experience working within cGMP and/or ISO-regulated environments
Strong documentation and recordkeeping skills
Good communication and teamwork abilities
Preferred
Experience within pharmaceutical, chemical, life sciences, or fine chemical manufacturing
Hands‑on experience with HPLC, GC, or laboratory analytical testing
Familiarity with ISO standards and regulatory audits
Experience using SAP
What We're Looking For
Strong attention to detail
Commitment to quality, safety, and compliance
Ability to work effectively in a team environment
Strong organizational and problem‑solving skills
Willingness to learn and grow within a quality‑focused operation
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Languages
- English
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