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Manager Of Quality Assurance Jobs (NOW HIRING)

GenScript/ProBio

Manager of Quality Assurance

Redmond, WA · 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 ...

Mantrose Group

Director of Quality Assurance

Elgin, IL · On-site

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 ...

CheltenHouse

QA Operations Manager

Bridgeport, NJ · 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 ...

TRC Talent Solutions

Director of QA

Beech Creek, PA

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 ...

Siegfried Ltd

Quality Assurance Manager

Pennsville, NJ · 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:

Synergy Family Services

$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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How much do manager of quality assurance jobs pay per year?

As of Aug 28, 2026, the average yearly pay for manager of quality assurance in the United States is $118,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $144,500.00 per year, depending on experience, location, and employer.

What does a manager of quality assurance do?

A Manager of Quality Assurance oversees the quality control processes within an organization to ensure products or services meet specified standards and comply with regulations. They develop testing procedures, lead quality assurance teams, analyze data, and implement improvements to enhance quality and efficiency. Their role may also include training staff, collaborating with other departments, and handling audits or customer complaints related to quality. Overall, they play a crucial role in maintaining the reputation and reliability of a company's offerings.

What are the key skills and qualifications needed to thrive as a manager of quality assurance?

To thrive as a Manager of Quality Assurance, you need a strong background in quality management systems, process improvement, and a relevant degree such as in engineering, science, or a related field. Familiarity with ISO standards, Six Sigma methodologies, audit tools, and quality management software is typically required, often supported by certifications like ASQ Certified Manager of Quality/Organizational Excellence. Leadership, problem-solving, and effective communication are crucial soft skills for motivating teams and ensuring compliance. These competencies are essential for driving continuous improvement, maintaining regulatory standards, and ensuring product or service excellence.

What are some common challenges faced by a manager of quality assurance when implementing new quality standards across teams?

A Manager of Quality Assurance often encounters resistance to change when introducing new quality standards, as team members may be accustomed to existing processes. Effective communication and training are crucial to ensure everyone understands the benefits and requirements of the updated standards. Additionally, coordinating across multiple departments to maintain consistency can be challenging, requiring strong collaboration and problem-solving skills. Regular monitoring, feedback, and adaptability help in overcoming these obstacles and fostering a culture of continuous improvement.

What is the difference between Manager Of Quality Assurance vs Quality Assurance Specialist?

AspectManager Of Quality AssuranceQuality Assurance Specialist
CertificationsISO 9001, Six Sigma, ASQ certificationsISO 9001, Six Sigma, ASQ certifications
Work EnvironmentOversees teams in manufacturing, software, or healthcare industriesPerforms testing and inspections within similar industries
ResponsibilitiesDevelops quality strategies, manages teams, ensures complianceExecutes testing, documents defects, supports quality improvements

The main difference is that the Manager Of Quality Assurance leads and manages quality teams and strategies, while the Quality Assurance Specialist focuses on executing testing and inspections. Both roles require similar certifications and work in comparable environments, but the manager has broader responsibilities for overseeing quality processes.

How much does a manager of quality assurance earn?

A manager of quality assurance typically earns between $70,000 and $120,000 annually, depending on experience, industry, and location. They often oversee quality control processes, implement standards, and may hold certifications like Six Sigma or ISO auditor credentials.

What cities are hiring for Manager Of Quality Assurance jobs?

Cities with the most Manager Of Quality Assurance job openings:

What are the most commonly searched types of Of Quality Assurance jobs?

The most popular types of Of Quality Assurance jobs are:

What states have the most Manager Of Quality Assurance jobs?

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Manager Of Quality Assurance jobs near you
Infographic showing various Manager Of Quality Assurance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $118,074 per year, or $56.8 per hour.

Manager of Quality Assurance

GenScript/ProBio

Redmond, WA • On-site

$100K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 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.

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