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Manager Of Qa Jobs (NOW HIRING)

Manager of Quality Assurance

Redmond, WA ยท On-site

$100K - $120K/yr

The QA Manager is accountable for ensuring consistent and harmonized execution of quality systems, including facility/utility/equipment qualification, quality systems establishment and maintenance ...

Manages all daily aspects of Quality Assurance, Quality Compliance and Document Management for Mantrose Group products, which includes Functional Systems (PFI and Holton), VerdeCoat, Mantrose-Haeuser ...

When you work as a Director of Quality Assurance at KCAS Bio, you have the opportunity to further ... While managing these responsibilities, you will also oversee the quality management system ...

Director of Quality Assurance

Columbus, OH ยท On-site

$90 - $120/hr

Director of Quality Assurance Regular Full-Time Columbus, OH, US Unique opportunity to join ... Manage electronic health records system and administration. EDUCATION/EXPERIENCE Knowledge and ...

QA Operations Manager

Bridgeport, NJ ยท On-site

$105K - $130K/yr

We are looking for a QA Manager of Production who will lead the execution of quality assurance ... systems across a multi-shift, fast-paced food manufacturing environment, ensuring compliance ...

Leadership- take ownership and be the catalyst of change. Enthusiasm- be motivated and passionate ... robust process capability, quality performance, and throughput. Ensure compliance with the ...

Quality Assurance Manager

Pennsville, NJ ยท On-site

$105 - $135/hr

Your Role:**The incumbent is responsible for the management of all aspects of Quality Assurance and provides daily support and supervision to the Quality Assurance Specialists.**Your Profile:

$120 - $180/hr

Design and manage an agency-wide quality assurance and performance improvement (QAPI) program ... Serve as a key member of the leadership team, actively contributing to strategic planning and ...

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Manager Of Qa information

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$24K

$86.2K

$158K

How much do manager of qa jobs pay per year?

As of Aug 29, 2026, the average yearly pay for manager of qa in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 per year, depending on experience, location, and employer.

What does a manager of QA do?

A Manager of QA (Quality Assurance) is responsible for overseeing the quality assurance processes within an organization. They lead QA teams, develop testing strategies, and ensure that products or services meet established quality standards before reaching customers. Their duties often include setting quality objectives, managing audits, training team members, and collaborating with other departments to resolve issues. The Manager of QA plays a crucial role in maintaining product reliability and customer satisfaction.

What are some common challenges faced by a manager of QA, and how can they be addressed?

Managers of QA often encounter challenges such as balancing the need for thorough testing with tight project deadlines, managing cross-functional communication, and ensuring consistent quality standards across multiple teams. Addressing these challenges involves implementing clear testing processes, fostering a culture of open communication with development and product teams, and continuously monitoring and improving QA methodologies. Leveraging automation and regularly training team members can also help maintain high efficiency and quality in fast-paced environments.

What are the key skills and qualifications needed to thrive as a manager of QA, and why are they important?

To thrive as a Manager of QA, you need expertise in quality assurance methodologies, testing processes, and a relevant degree in computer science or a related field. Familiarity with test management tools (like Jira, TestRail), automation frameworks, and certifications such as ISTQB are often required. Strong leadership, communication, and problem-solving skills help drive team performance and foster effective cross-departmental collaboration. These skills and qualifications ensure the delivery of high-quality products, minimize defects, and support organizational goals for software excellence.

What is the difference between Manager Of Qa vs Quality Assurance Analyst?

AspectManager Of QaQuality Assurance Analyst
Required CredentialsBachelor's degree in Computer Science or related field; often requires experience in QA managementBachelor's degree in Computer Science, Engineering, or related field; certifications like ISTQB are common
Work EnvironmentLeads QA teams, manages testing processes, and oversees quality strategiesPerforms testing, documents defects, and executes test cases under supervision
Employer & Industry UsageUsed in software development, IT, and tech companies for leadership rolesCommon in software firms, tech companies, and product development teams

The Manager Of Qa typically oversees the entire QA process and manages teams, requiring leadership experience. In contrast, a Quality Assurance Analyst focuses on executing tests and identifying defects. Both roles are essential in software quality assurance but differ in scope and responsibilities.

What cities are hiring for Manager Of Qa jobs?

Cities with the most Manager Of Qa job openings:

What are the most commonly searched types of Of Qa jobs?

The most popular types of Of Qa jobs are:

What states have the most Manager Of Qa jobs?

States with the most job openings for Manager Of Qa jobs include:

Infographic showing various Manager Of Qa job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

Manager of Quality Assurance

GenScript/ProBio

Redmond, WA โ€ข On-site

$100K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 23 hours ago


Job description

About GenScript
Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.
The position reports to the Senior Vice President of the Innovation Center and is responsible for the strategic development and operational management of the site's ISO 9001-certified Quality Management System (QMS). The QA Manager is accountable for ensuring consistent and harmonized execution of quality systems, including facility/utility/equipment qualification, quality systems establishment and maintenance, raw material management, production process support, product release, deviation and CAPA management, change management, and risk management across the Seattle, WA site.
The role will ensure consistent execution of quality systems across the Seattle site covers multiple production lines, QC groups, and R&D teams.
  1. Based on corporate policies, develop the QMS strategy and establish quality procedures to support RUO production and R&D activities at the Seattle site.
  2. Customer & ISO Audits: Lead and host frequent customer audits and ISO 9001 surveillance audits. Act as the primary face of Quality for the site, effectively demonstrating the robustness of our QMS to external partners
  3. Supplier Qualification: Manage the site's supplier qualification lifecycle. Evaluate, approve, and continuously monitor external providers of raw materials and services through questionnaires, audits, and performance tracking to ensure ISO 9001 compliance.
  4. Customer Quality Agreements: Negotiate and manage Customer Quality Agreements (CQAs) and efficiently handle customer supplier questionnaires, ensuring alignment between client expectations and our RUO manufacturing standards.
  5. R&D and Tech Transfer: Partner with the R&D teams to support new technology development, ensuring seamless tech transfer. Review and approve R&D SOPs, reports, and risk assessments promptly to maintain the agility required for RUO environments without creating bureaucratic bottlenecks.
  6. Provide cross-site quality leadership for QMS lifecycle maintenance, raw material management, final product release, supply chain, automation, manufacturing, validation, and facility engineering across all 3 production lines.
  7. Apply Quality by Design principles to define robust, integrated control strategies for the oligonucleotide, synthetic gene, mRNA, and formulation manufacturing processes.
  8. Oversee and manage the execution of quality systems during daily production activities to ensure the delivery of high-quality RUO molecular biology products.
  9. Present updates to project or upper management teams on progress and enforcement of quality improvement and manufacturing support activities.

Qualifications:
  1. Master's degree in a life sciences-related field (or equivalent) with 5+ years of QA/QC experience in a biotech production environment, including substantial management responsibility.
  2. Experience with molecular biology product manufacturing (oligonucleotides, synthetic gene, mRNA) or formulation services is highly desirable.
  3. Completed Lead Auditor training or possesses deep working knowledge of ISO 9001:2015 standards.
  4. Extensive experience hosting external customer audits and filling out supplier quality questionnaires in a B2B life sciences or CRDMO environment.
  5. Experience drafting and negotiating Quality Agreements with clients, with a strong ability to manage customer expectations appropriately for an RUO setting.
  6. Expert knowledge of quality risk assessment, CAPA management, and change control methodologies within an RUO or ISO-certified manufacturing environment.
  7. Proven track record in establishing or optimizing a quality organization and working collaboratively with R&D, production, and QC groups.
  8. Excellent diplomacy, negotiation, and customer-service skills, with the ability to confidently explain and defend quality systems to technical and quality representatives from partner organizations.
  9. Strong interpersonal, verbal, and written communication skills.

Benefit:
  • Medical Insurance/ Vision Insurance/ Dental Insurance
  • 401(k) & Retirement Savings Plan (RSP)
  • Short Term Disability Insurance
  • New Child Leave
  • Paid Time Off
  • Paid Company Holidays per year
  • Paid Sick Days (earned based on hours worked)
  • Compassionate Leave
  • Jury Duty Leave
  • Float day
  • Personal days

Perks:
  • Free colleague meals during shift
  • Onsite massages Charis
  • Onsite gyms

Compensation:
Salary range: $100,000 - $120,000 total compensation, including bonus, depending on experience and qualifications.
Benefits:
Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.