Quality Compliance Engineer
Listed on 2026-08-02
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Quality Compliance Engineer
Quality Assurance
Los Angeles, California, US
Pay Rate Low: 90000 | Pay Rate High: 120000
Our client is a global, publicly traded bioscience leader dedicated to advancing human health-span and healthy aging through strategic, world-class research collaborations.
Title: Quality Compliance Engineer
Location: Hybrid – Tustin, CA
Schedule: M-F, 8-5pm. This is a hybrid position. 3 days onsite is a must.
Salary: $90K–$120K + flexibility for strong candidates
Direct Hire
We are seeking a Quality Engineer to support quality operations, process improvements, and regulatory compliance in a fast-paced environment. This role will partner cross-functionally to ensure products meet the highest standards for safety, quality, and compliance.
Key Responsibilities- Lead investigations into manufacturing deviations, nonconformances, and process defects, including root cause analysis and CAPA implementation
- Drive continuous improvement initiatives using quality metrics, data analysis, and operational KPIs
- Support SOP development and process optimization initiatives
- Conduct risk assessments (FMEA), supplier qualifications, and co-manufacturer audits
- Manage product specifications, third-party certifications (NSF, Halal, Kosher), and recall/mock recall activities
- Perform quality assessments for new formulas/products to ensure regulatory compliance
- Collaborate closely with internal teams, external partners, and suppliers
- BS degree in Biology, Chemical Engineering, or related scientific field
- 3+ years of Quality Engineering/QA experience within pharmaceuticals, CDMO, medical device, food, cosmetics, or dietary supplements
- Strong GMP/GDP knowledge and experience with FDA regulations (21 CFR 111, 117, 210, 211) and Quality Systems
- Hands‑on experience with investigations, deviations, CAPAs, supplier qualification, and auditing
- Data‑driven mindset with experience using metrics and statistical methods/Six Sigma toolsndli>
- Strong communication and cross‑functional collaboration skills
- Ability to travel up to 25% domestically with occasional international travel
- Pharmaceutical industry experience strongly preferred (in‑house or CDMO environment)
- Experience in fast‑paced manufacturing or regulated environments
- Must be authorized to work in the US.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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