Free Professional QA Specialist Resume Template

Free Professional QA Specialist Resume TemplateFree Professional QA Specialist Resume TemplateOur 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.Create ResumeProfessional QA Specialist ResumeCustomize ResumeIndustry SnippetsBy reading our free creative QA specialist resume template, you will learn how to emulate the best parts of it. Professional Resume Pros and ConsThis 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 applicationsCons Do you have gaps in your employment history? T his will make them obviousCons You dont get to share your personalityResume TextJAMESBUFORD123 Street,City, ST, 12345 H (123) 456-7890 C (123) 456-7890 emailleisp.comProfessional SummaryResults-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 HighlightsPharmaceutical Quality ManufacturingCurrent Good Manufacturing Practices (cGMP)Good Documentation ProcessesQuality Systems ManagementRegulatory ComplianceCorrective an d Preventive Action PlanningProfessional ExperienceQuality Assurance Specialist10/1/2010 CurrentTedor Pharma, Inc. Cumberland, RIWork with QA Director to establish and maintain Tedors 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 Associate9/1/2002 9/1/2010PharmaCorp New Brunswick, NJSupported 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, includ ing GMP materials release, shipment verification, and wertzuwachs of line clearances in Class 100,000 environment.Quality Assurance Specialist6/1/2000 9/1/2002Pharma Care Industries Hauppauge, NYPerformed 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 RD Partners, and Quality Assurance Specialist at Ferring Pharmaceuticals.Education and CertificationMaster of Arts Chemistry and BiochemistryQueens College, City University of New York Queens, NYBachelor of Arts Chemistry and BiochemistryQueens College, City University of New York Queens, NYRe gulatory Affairs Certificate PharmaceuticalsCertified Quality Auditor