QA Coordinator (Contract) GMP / Quality Operations

QA Coordinator (Contract)•GMP / Quality Operations Recruits Lab Carpinteria, CA Job Details Full-time | Contract $23 an hour 3 days ago Qualifications GMP High school diploma or GED Cross-functional communication Full Job Description 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) 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 Schedule Full-Time Contract Monday•Friday 3:00 PM•11:30 PM (2nd Shift) Compensation Competitive hourly compensation $23/hr #LI-DN1