QA Specialist
Job Description
QA Specialist
SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
- Title: QA Specialist
- Location: Houston, TX
- Industry: Pharmaceutical
- Hours: M-F: 8-5
- Salary: up to $50.00/ hr Paid Weekly (Benefits are Available)
- Employment Type: 6 month Contract
Environment: A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. Headquartered in Basel, Switzerland, the company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R&D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.
Key responsibilities:
- Facilitates the implementation of quality systems and compliance initiatives projects at the site
- Identifies, maintains and reports site quality KPIs for Quality Council
- Responsible for ownership of the site s Quality Council program, including hosting and ensuring participation of SMEs in monthly Quality Council meetings
- Reports site quality KPIs in KPI reporting system monthly
- Identifies actions required to meet site KPI targets and facilitates with SMEs activities necessary to meet those targets
- Supports and hosts change controls review board, deviation review board and CAPA review board.
- Responsible for site monthly and quarterly trending program and associated reports
- Identifies and facilitates execution of CAPAs related to identified trends
- Revise or approve quality records (change controls, deviations/ investigations, CAPAs and controlled documents-SOPs, forms, etc., related to compliance or risk management program.
Key requirements:
- Minimum 5 years experience
- cGMP environment and related QA field
- Must have KPI and/or KQI experience
- Must have Trackwise experience
- Must be proficient in Excel
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For more than 30 years, SRG4 has worked with clients in Fortune 100 corporations, as well as emerging and rapid growth companies, located throughout the United States and globally.
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