A traditional QA specialist resume is about as straightforward as it gets. This format emphasizes you and your accomplishments, without fancy graphic flourishes. Instead, you can use space to share your professional accomplishments. Take time to look over the sample provided for further insights.
By looking over the traditional QA specialist resume template, you will see the ways that you too can add value to your own resume.
Traditional Resume Pros and Cons
This particular format is meant to assist job seekers who want to share their achievements and special skills in a narrative format. The style is widely accepted, but is especially great for more traditional companies. See the pros and cons to determine if this resume design fits your needs.
- Pros: The organization is excellent
- Pros: You can easily edit the resume to apply for multiple jobs
- Cons: You might find yourself with too much space on the page
- Cons: Doesn’t allow you to show off your personality
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Quality Assurance Specialist with a track record of success in maintaining high-reaching QA and QC standards within various healthcare sectors. Experienced in writing standard operating procedures, testing randomized samples, CAPA management, and coordinating and supporting internal and external audits. Comprehensive understanding of accreditation guidelines and regulatory, industry, and corporate requirements. Accomplished in strategically improving QC procedures and streamlining manufacturing.
Laboratory Quality Systems Management
Corrective and Preventive Action Planning
Internal and External Audits
Good Documentation Practices
Quality Assurance Specialist
10/1/2010 – Current
Athena Surgical – San Francisco, CA
Review device history records for disposable devices, RF controllers, and related accessories.
Release product for clinical and commercial distribution.
Contribute to design history file reviews to ensure completion and conformance with required deliverables.
Schedule calibration and preventive maintenance activities; follow up on out of tolerance investigations.
Initiate non-conforming material reporting NCRs and complete verification activities; schedule environmental monitoring activities and review associated records.
Collect and prepare analysis of quality data for trend reviews and management review meetings.
Assist with preparations for internal and external quality audits and prepare corrective and preventive action requests.
Quality Assurance Associate
9/1/2002 – 9/1/2010
Vanguard Genetics – San Jose, CA
Developed, implemented, communicated, and maintained comprehensive quality plan.
Defined and maintained QA/QC objectives, targets, and processes, and reviewed new targets, protocols, processes, equipment, supplies, and technologies for quality standards.
Assisted in maintaining College of American Pathologists (CAP) and UK Clinical Pathology Accreditation (CPA) standards.
Established QC/QA documentation procedures and monitored related performance.
Ensure proper qualification, maintenance, and calibration of lab equipment and online test instruments.
Performed regular internal quality audits, recommended improvements, and initiated corrective and preventive actions.
Quality Assurance Specialist
6/1/2000 – 9/1/2002
PharmaCorp – Santa Barbara, CA
Provided QA oversight of clinical manufacturing of final drug product and identified and assessed quality risk in activities and processes according to regulatory guidelines and standard operating procedures.
Ensured manufacturing conformed with regulatory and good manufacturing practices guidelines.
Investigated quality deviations, GMP and quality system issues, non-conforming materials, and CAPA.
Education and Training
Bachelor of Arts: Chemistry and Biochemistry
University of California, Santa Barbara — Santa Barbara, CA
Regulatory Affairs Certificate: Pharmaceuticals
Certified Quality Auditor
American Society for Quality Member