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Manager Quality Assurance Jobs (NOW HIRING)

Sotera Health

Manager Quality Assurance

Rockaway, NJ

$92K - $149K/yr

Reporting to the General Manager, the Quality Assurance (QA) Manager is directly responsible for managing and coordinating all quality functions for the facility. He/She maintains responsibility for ...

Alphapointe

Manager, Quality Assurance

Kansas City, MO · On-site

$65K - $80K/yr

Be on-site internal quality assurance manager throughout ISO 9001-2015 surveillance and re-certification audits, certification and future re-certification process by performing internal audits ...

Verano

Manager, Quality Assurance

Canton, OH · On-site

$60K/yr

Job Summary The Quality Assurance Manager will be responsible for the management of the quality assurance activities for the facility in accordance with the Company's policies, principles, and ...

Justworks

Manager, Quality Assurance

New York, NY · On-site

Provide guidance, coaching, and performance management to ensure high-quality analysis and reporting * Foster a culture of curiosity, accountability, and continuous learning within the QA team How ...

Planet DDS

Manager, Quality Assurance

$118K - $165K/yr

Overview The Manager of Quality Assurance , will lead our QA team and ensure the delivery of high-quality, reliable, and scalable software products. This role will drive innovation in test automation ...

Planet DDS

Manager, Quality Assurance

Atlanta, GA

$118K - $165K/yr

Overview The Manager of Quality Assurance , will lead our QA team and ensure the delivery of high-quality, reliable, and scalable software products. This role will drive innovation in test automation ...

Verano

Manager, Quality Assurance

Canton, OH

$60K/yr

Job Summary The Quality Assurance Manager will be responsible for the management of the quality assurance activities for the facility in accordance with the Company's policies, principles, and ...

Alphapointe

Manager, Quality Assurance

Kansas City, MO

$65K - $80K/yr

Be on-site internal quality assurance manager throughout ISO 9001-2015 surveillance and re-certification audits, certification and future re-certification process by performing internal audits ...

LGM Pharma, LLC

MANAGER, QUALITY ASSURANCE

Taylor, MS · On-site

$95K - $110K/yr

Prepare QA reports and provide data to support cross-functional business needs * Oversee management of deviations, CAPAs, and change controls in a timely and compliant manner * Support customer ...

AMRESCO

Manager, Quality Assurance

Phillipsburg, NJ

$97K - $156K/yr

The Quality Assurance Manager (Manufacturing) is responsible for oversight of quality assurance activities related to the business operations units, as defined by the quality management system ...

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How much do manager quality assurance jobs pay per year?

As of Aug 4, 2026, the average yearly pay for manager 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 development and implementation of quality standards and procedures to ensure products or services meet company and industry requirements. They lead quality teams, analyze data to identify issues, and coordinate testing and inspection processes, often using tools like quality management systems. Strong leadership, communication, and knowledge of industry regulations are essential for this role.

What are the key skills and qualifications needed to thrive as a Manager Quality Assurance?

To thrive as a Manager Quality Assurance, you need a solid background in quality management systems, process improvement, and industry-specific regulations, often supported by a relevant degree and experience in quality roles. Familiarity with tools like Six Sigma, ISO standards, statistical analysis software, and quality audit systems is typically required. Strong leadership, problem-solving, and communication skills help drive continuous improvement and foster a culture of quality within teams. These competencies are crucial for ensuring product or service excellence, regulatory compliance, and operational efficiency.

What are some common challenges faced by a Manager Quality Assurance, and how can they be addressed?

A Manager Quality Assurance often faces challenges such as aligning quality standards across departments, managing tight deadlines, and ensuring regulatory compliance. To address these, it's important to foster clear communication between teams, establish robust quality management systems, and provide ongoing training. Proactively identifying potential issues and encouraging a culture of continuous improvement can also help minimize defects and boost overall team performance.

What are the roles and responsibilities of a Manager Quality Assurance?

A Manager of Quality Assurance oversees the quality control processes within an organization to ensure that products or services meet established standards and customer expectations. They develop and implement quality management systems, lead quality audits, and supervise QA teams. Additionally, they analyze data to identify trends or areas for improvement, work with other departments to resolve quality issues, and ensure compliance with industry regulations and certifications.

Is a quality assurance manager a stressful job?

A quality assurance manager often faces stress related to meeting strict quality standards, tight deadlines, and managing team performance. The role requires attention to detail, problem-solving skills, and sometimes long hours during product launches or audits, which can contribute to job-related stress.

What do quality assurance managers do?

Quality assurance managers oversee the testing and inspection of products or services to ensure they meet quality standards and customer expectations. They develop quality control procedures, analyze data to identify issues, and coordinate with teams to implement improvements, often using tools like quality management systems and industry certifications. Their role involves continuous monitoring and reporting to maintain product consistency and compliance.
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What cities are hiring for Manager Quality Assurance jobs? Cities with the most Manager Quality Assurance job openings:
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Manager Quality Assurance jobs near you
Infographic showing various Manager Quality Assurance job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $118,074 per year, or $56.8 per hour.

Manager, Quality Assurance

Rhythm Pharmaceuticals

Boston, MA • On-site

$110K - $165K/yr

Full-time

Re-posted 18 days ago

Job description

Company Overview
Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.
Opportunity Overview
Rhythm is looking for a Manager Quality Assurance (QA) to play a key role in ensuring quality and regulation-based compliance during the manufacture and distribution of Rhythm clinical products. This is an individual contributor management-level role within a CDMO dependent Quality organization. It requires solid technical expertise in sterile pharmaceutical manufacturing, strong CDMO relationship management skills, and fluency in the regulatory expectations for clinical-stage parenteral products. The successful candidate will operate with a high degree of autonomy and will partner closely with CMC development, Regulatory Affairs, Clinical Supply Chain, and CDMO Quality and manufacturing teams. The Manager QA will report to the Director, CMC QA, based in The United States, while supporting and liaising with global functions at Rhythm.
Responsibilities and Duties
  • Serve as the quality contact for external manufacturing partners producing sterile drug products, establishing and maintaining quality oversight of clinical manufacturing activities.
  • Manages clinical lot disposition for sterile drug product, including review of batch records, analytical results, and compliance with Regulatory Dossiers.
  • Responsible for the review and approval of process validation documents, protocols and reports, Master Batch Records and Executed Batch Records at the Contract Development and Manufacturing Organization (CDMO).
  • Provides QA oversight during technology transfer activities for new clinical products moving into CDMO sites.
  • Monitors contract manufacturer performance through routine reviews, meetings, and quality metrics.
  • Utilizes GMP-regulated quality management systems, including document control, change control, deviations/complaints, and corrective and preventative actions (CAPAs).
  • Facilitates the creation, review, and approval of relevant SOPs and work instructions relevant to CMC activities.
  • Provides QA support during CDMO audits, including participating in audit execution.
  • Supports regulatory filings (e.g., Investigational New Drugs (INDs), Annual Reports, Stability Reports) by reviewing data, ensuring compliance with regulatory procedures.

Qualifications and Skills
Required
  • Bachelor's degree in a scientific discipline (Chemistry, Biology, Engineering, or related field)
  • A minimum of 5 years of relevant experience in the pharmaceutical industry, with established Quality and Compliance knowledge in supporting manufacturing of sterile products.
  • Demonstrated experience providing sponsor-side quality oversight of CDMOs for sterile drug products, including batch record review, batch disposition, deviation management, and quality governance.
  • Working knowledge of aseptic processing, media fills, environmental monitoring, and sterility as applied in a CDMO model.
  • Strong understanding of cGMP regulations including FDA CFR Parts 210/211, EU Annex 1, ICH Q7, Q8, Q9, and Q10.
  • Detail oriented with strong organizational skills and the ability to manage multiple clinical programs and CDMO relationships simultaneously.
  • Self-directed and comfortable with a high degree of autonomy in a small-time, high-accountability environment.

Preferred
  • Experience with technology transfer of sterile Drug Products into new CDMO sites.
  • Experience with lyophilized products, pre-filled syringes, or other complex sterile dosage forms; experience in peptides is a plus.
  • ASQ Certified Quality Auditor (CQA) or similar.

This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a hybrid-work model. Candidates applying must be willing and able to be in the Boston office in coordination with their department and business needs. This role may involve some travel.
The expected salary range for this position is $110,000 - $165,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This role may be eligible for benefits and other compensation such as restricted stock units.
More about Rhythm
We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.
At Rhythm our core values are:
  • We are committed to advancing scientific understanding to improve patients' lives
  • We are inspired to tackle tough challenges and have the courage to ask bold questions
  • We are eager to learn and adapt
  • We believe collaboration and ownership are foundational for our success
  • We value the unique contribution each individual brings to furthering our mission

Inherent in our core values is the commitment to act ethically and with integrity in all we do.
Rhythm is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law.
Headquartered in Boston, Rhythm is proud to have been named one of the Top Places to Work in Massachusetts.

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