QA Specialist

Tampa, FL

Posted: 03/16/2022 Job Number: JN -032022-14326 Division: Life Sciences

Job Description

QA Specialist II

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 II

Location: Tampa, FL

Industry: Pharmaceutical

Hours: Mon-Fri 7:00am-3:30pm

Salary: $44.49/HR (Benefits are Available)

Employment Type: Long Term Contract - Possible Extend

Environment: This client is one the world s leading suppliers to the pharmaceutical, biotech and specialty ingredients markets. We create products that support a healthier lifestyle and enhance ones quality of life.

Key responsibilities:

  • Verification of the company's compliance with ISO/cGMP quality system requirements as well as knowledge of PICS Guide to Good Manufacturing Practices Part 1 and 2 or the EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use, including Annex 1.
  • Provide immediate support to operations and quality control staff to address compliance related concerns (QA on-the-floorsupport).
  • Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams.
  • Audit internal quality system elements in manufacturing and operational support areas.
  • Provide oversight for compliance of Change Controls, CA/PA and investigations, OOS and deviations.
  • Perform external audits of suppliers/vendors/off-site facilities.
  • Act as a customer interface during on-site audits, conference calls and other standard means of communication.
  • Independently identify and manage special projects or QA compliance functions as agreed upon with QA management.
  • Prioritize and manage a variety of projects simultaneously. May need to lead and direct the work of others. Review and approve validation documents.
  • Review and Master Batch Records (MBR) and supporting documents. Perform review/release of batch records, as needed.

Key requirements:

  • Direct QA commercial drug substance/drug product experience required or an equivalent amount of aseptic processing and cell therapy manufacturing experience.
  • GMP compliance and Part 11 compliance knowledge preferred.
  • Experience with oversight of aseptic processing and the associated international aseptic processing regulations.
  • Excellent written and oral communication to include accurate and legible documentation skills; ability to work in a fast-paced environment; team oriented; independent work skills and a strong work ethic.
  • The ability to interface and communicate directly with clients is required.
  • Microsoft Office and database management skills, organization skills, record keeping skills and ability to handle multiple projects.
  • 3-5 Years' Experience


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