Приклад CV для Quality Assurance Manager

Choose the right format for a Quality Assurance Manager resume

Use a reverse-chronological format. Hiring managers in manufacturing, pharma, medical devices, and software expect to see your most recent role first and want a clear progression from individual contributor to supervisory or managerial responsibility. A functional or hybrid format raises red flags unless you are making a significant industry pivot.

Keep the resume to two pages maximum. One page works only if you have fewer than eight years of experience. Use 0.75-inch margins, a clean sans-serif font like Calibri or Arial at 10–11pt, and clear section headers. ATS systems used by companies like Workday, Taleo, and iCIMS parse standard headers reliably, so avoid text boxes or tables for your main content.

• Place your name, city/state, phone, LinkedIn URL, and a professional email in the header — no full street address required
• Use consistent date formatting: Month YYYY – Month YYYY
• Keep section order: Summary → Work Experience → Skills → Certifications → Education

Write a professional summary that frames your QA expertise immediately

Your summary is three to four lines at the top of the resume. It should name your years of experience, the industries you've worked in, the quality systems you manage, and one or two measurable outcomes. Generic phrases like 'detail-oriented professional' waste prime real estate.

Example: "Quality Assurance Manager with 11 years of experience in FDA-regulated medical device manufacturing. Oversees a 14-person QA team and maintains ISO 13485 and 21 CFR Part 820 compliance across three production facilities. Reduced customer complaint rate by 34% over two years by implementing a corrective and preventive action (CAPA) tracking system in ETQ Reliance. Experienced in supplier qualification, internal auditing, and NPI quality planning."

Write work-experience bullets that show impact, not just duties

Every bullet should follow an action verb → task → measurable result structure. QA managers have access to concrete data — defect rates, audit findings, CAPA closure times, yield percentages, cost of poor quality (COPQ) — so use them. Recruiters in this field are skeptical of bullets that describe responsibilities without outcomes.

Avoid listing software or standards in isolation inside bullets; instead, show what you did with them and what changed as a result.

• Reduced incoming inspection rejection rate from 8.2% to 1.9% over 18 months by redesigning supplier scorecards and conducting quarterly on-site audits at the top 12 vendors
• Led preparation for a zero-finding FDA 483 inspection across two sites by closing 47 open CAPA items and retraining 200+ employees on updated SOPs within a 90-day remediation window

Include the skills and certifications recruiters and ATS systems look for

Quality assurance job postings are heavily keyword-driven. A dedicated Skills section lets ATS parse your competencies before a human reads the document. Separate hard skills from soft skills, and list certifications in their own subsection with the issuing body and year obtained.

Prioritize the tools and frameworks that appear most often in postings for your target industry: pharma and medical devices weight regulatory knowledge heavily, while software QA roles emphasize test management platforms and agile methodology.

• Certifications: ASQ Certified Quality Manager (CQM/OE), ASQ Certified Quality Auditor (CQA), Six Sigma Black Belt (CSSBB), ISO 9001/13485 Lead Auditor (BSI, Bureau Veritas, or DEKRA), PMP if managing large quality projects
• Quality systems & standards: ISO 9001, ISO 13485, IATF 16949, 21 CFR Part 820, AS9100, cGMP, GLP
• Tools & software: ETQ Reliance, MasterControl, Veeva Vault QMS, SAP QM, Minitab, JIRA (for software QA), TestRail, FMEA, SPC, MSA
• Core competencies: CAPA management, root cause analysis (RCA), supplier quality management, internal and third-party auditing, risk management (ISO 14971), NPI quality planning, SOP development

Education, licenses, and additional sections that strengthen the resume

Most QA Manager roles require a bachelor's degree in engineering, life sciences, chemistry, or a related technical field. An MBA or master's in quality management can differentiate you for director-level roles but is rarely required. List your degree, institution, and graduation year; GPA is optional and only worth including if above 3.5 and within the last five years.

Add a brief Professional Development or Training section if you have completed relevant coursework through ASQ, RAPS (for regulatory affairs overlap), or IAQG. If you hold an active FDA inspector credential or have served as a notified body auditor, list that explicitly — it is rare and highly valued. A Publications or Conference Presentations section is appropriate if you have presented at ASQ World Conference or similar events.

• List ASQ membership and any section leadership roles — it signals active engagement with the profession
• Include language proficiency if you audit international suppliers
• Omit references, headshots, and unrelated certifications

Mistakes to avoid

• ×Listing quality standards like ISO 9001 or 21 CFR Part 820 without explaining the scope of your involvement — recruiters need to know whether you built the system, maintained it, or simply worked within it.
• ×Using vague audit language such as 'participated in audits' instead of specifying your role as lead auditor, auditee liaison, or CAPA owner and stating how many audits you conducted per year.
• ×Omitting metrics entirely, which is a credibility problem in QA because the entire discipline is measurement-driven — every role generates data on defect rates, yield, CAPA cycle time, or cost of poor quality.
• ×Failing to tailor the resume to the industry vertical — a resume optimized for automotive IATF 16949 will underperform for a pharma cGMP role if you do not reframe your experience around FDA regulatory language and validation protocols.

Frequently asked questions

Do I need a Six Sigma certification to get a Quality Assurance Manager job?

It depends on the industry and company. Manufacturing, automotive, and aerospace employers frequently list Six Sigma Green Belt or Black Belt as preferred or required, while software QA and smaller companies rarely require it. If you lack the certification but have applied the methodology — running DMAIC projects, using Minitab for SPC — describe that experience explicitly in your bullets and note any in-progress training.

How do I show QA leadership experience if I managed a small team or no direct reports?

Emphasize cross-functional leadership: audit teams you led, corrective action councils you chaired, supplier qualification projects you owned, or training programs you developed and delivered. Quantify the scope — number of employees trained, number of suppliers qualified, number of audit findings resolved — to demonstrate influence beyond a formal headcount.

Should I include every quality standard I have ever been exposed to in my skills section?

No. List only standards where you can speak to specific responsibilities in an interview — auditors and hiring managers will probe your depth on anything you claim. If you are applying for a role that requires IATF 16949 experience and you only have peripheral exposure, note it honestly as 'familiarity' or leave it off rather than risk a credibility problem in the screening call.