Free Professional QA Specialist Resume Template

Our professional QA specialist resume template keeps things, well, professional. With its superb organization and neat layout, employers will know that you take this opportunity seriously. Take a look at the example to see how you can write and format a your own.


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Industry Snippets

By reading our free creative QA specialist resume template, you will learn how to emulate the best parts of it.

Professional Resume Pros and Cons

This specific template is perfect for applicants who want to come across as serious and polished. Traditional companies will especially favor this template design. Even so, consider the pros and cons before choosing this style for your resume.

  • Pros: Simple organization is easy for employers to dissectPros: Easy to edit, so you can use it for multiple job applications
  • Cons: Do you have gaps in your employment history? This will make them obvious
  • Cons: You don’t get to share your personality

Resume Text
123 Street,
City, ST
H: (123) 456-7890
C: (123) 456-7890
Professional Summary
Results-oriented Quality Assurance Specialist with over 20 years of experience in pharmaceutical manufacturing and proven track record of success in administering quality systems. Expertise in coordinating quality control testing, improving quality control procedures, and streamlining manufacturing through the creation and implementation of high-reaching quality assurance processes. In-depth knowledge of cGMP, regulatory, industry, and corporate guidelines and requirements. Proven leadership skills with the ability to provide guidance and mentorship to junior staff to achieve business objectives and manufacturing goals.
Skill Highlights
Pharmaceutical Quality Manufacturing
Current Good Manufacturing Practices (cGMP)
Good Documentation Processes
Quality Systems Management
Regulatory Compliance
Corrective and Preventive Action Planning
Professional Experience
Quality Assurance Specialist
10/1/2010 ? Current
Tedor Pharma, Inc. ? Cumberland, RI
Work with QA Director to establish and maintain Tedor’s quality systems, including coordinating pharmaceutical quality system activities for review, approval, and disposition of intermediates and drug products for clinical trials and commercial use.
Spearhead and support investigation/CAPA activities relating to product release such as conducting and producing investigation reports, coordinating corrective and preventive action execution, managing change controls, and performing CAPA effectiveness checks.
Audit contract packaging sites to monitor and assure adherence to pharmaceutical quality system requirements.
Ensure facility compliance with cGMP and FDA regulations, best practices, and standards of quality.
Write, review, and approve deviations, corrective and preventive actions, change controls, specifications, standard operating procedures, test methods, stability and process protocols, and test results.
Review and validate labeling and distribution documentation.
Manage equipment calibration, qualification, and maintenance program.
Quality Assurance Associate
9/1/2002 ? 9/1/2010
PharmaCorp ? New Brunswick, NJ
Supported quality systems to advance development and manufacture of drug candidates; reviewed and approved data and documents, supported GMP manufacturing, and assisted with internal auditing.
Reviewed and approved executed batch records, liaised between Manufacturing and QA during batch record reviews, and facilitated communication between QA and client.
Uncovered opportunities for process or quality improvement and submitted recommendations to production coordinators to improve batch records for future use.
Maintained QA logbooks for document change control, instrument calibration schedules, stability pull schedules, test method and technical reports, and certificates of analysis.
Provide support to GMP manufacturing activities, including GMP materials release, shipment verification, and performance of line clearances in Class 100,000 environment.
Quality Assurance Specialist
6/1/2000 ? 9/1/2002
Pharma Care Industries ? Hauppauge, NY
Performed incoming inspection and QA release of raw materials and components, and reviewed batch records for final QA release of finished products.
Upheld and reinforced compliance with cGMP, including Good Documentation Processes and existing SOPs.
Coordinated with Operations personnel to identify and resolve internal quality issues.
Assisted with internal and vendor audits, including pre-audit preparations.
Past experience includes Quality Assurance Associate III at PCT, Quality Assurance Specialist at R&D Partners, and Quality Assurance Specialist at Ferring Pharmaceuticals.
Education and Certification
Master of Arts: Chemistry and Biochemistry
Queens College, City University of New York Queens, NY
Bachelor of Arts: Chemistry and Biochemistry
Queens College, City University of New York Queens, NY
Regulatory Affairs Certificate: Pharmaceuticals
Certified Quality Auditor