More jobs:
QA Coordinator GMP/Quality Operations
Job in
Carpinteria, Santa Barbara County, California, 93014, USA
Listed on 2026-06-21
Listing for:
Frey Consulting Group
Full Time, Contract
position Listed on 2026-06-21
Job specializations:
-
Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager, Quality Engineering -
Manufacturing / Production
QA Specialist / Manager, Quality Engineering
Job Description & How to Apply Below
QA Coordinator (Contract) – GMP / Quality Operations
Location:
Carpinteria, CA (On-Site)
Shift: 2nd Shift | 3:00 PM – 11:30 PM
Duration:
Contract through December 2026 (with potential extension)
Schedule:
Full-Time (40 hours/week)
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
- 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
- Experience with in 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
- 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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