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Pharmaceutical Quality Manager Jobs (NOW HIRING)

A minimum of 5-8 years of quality assurance experience in a medical device, pharmaceutical, or regulated manufacturing environment. * A minimum of 1-3 years' experience managing quality team members.

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. The Quality Manager is responsible for establishing ...

Quality Manager

Madison, NJ ยท On-site

$120K - $156K/yr

General Description The Quality Manager owns quality across multiple Stephen Gould branches - the ... Experience in regulated industries - medical device, pharmaceutical, cosmetics, or food-contact ...

Quality Manager Lead Quality Excellence in a Growing Life Sciences Manufacturing Environment Are ... Experience in life sciences, pharmaceutical, biotechnology, or regulated manufacturing environments.

... pharmaceutical, glass, metals, and utilities industries. We also deliver equipment for use ... Job Summary: As the Quality Manager, you will lead all aspects of the Quality function at your ...

... pharmaceutical, glass, metals, and utilities industries. We also deliver equipment for use ... Job Summary: As the Quality Manager, you will lead all aspects of the Quality function at your ...

Description Quality Manager Lead Quality Excellence in a Growing Life Sciences Manufacturing ... Experience in life sciences, pharmaceutical, biotechnology, or regulated manufacturing environments.

As the Quality Manager for our Wilson, NC site, you will lead and mentor the onsite Disposable ... Experience in life sciences, pharmaceutical, biotechnology, or regulated manufacturing environments.

... pharmaceutical, glass, metals, and utilities industries. We also deliver equipment for use ... Job Summary: As the Quality Manager, you will lead all aspects of the Quality function at your ...

... pharmaceutical, glass, metals, and utilities industries. We also deliver equipment for use ... Job Summary: As the Quality Manager, you will lead all aspects of the Quality function at your ...

... pharmaceutical, glass, metals, and utilities industries. We also deliver equipment for use ... Job Summary: As the Quality Manager, you will lead all aspects of the Quality function at your ...

... pharmaceutical, glass, metals, and utilities industries. We also deliver equipment for use ... Job Summary: As the Quality Manager, you will lead all aspects of the Quality function at your ...

... Pharmaceutical & IT services to a diverse set of customers across various industries around the ... Supplier Quality Manager Detailed Coordinate completion of Specification Agreements with suppliers.

Quality Manager

Torrance, CA ยท On-site

$96K - $128K/yr

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the ... Manage supplier quality, including audits, corrective actions, and performance monitoring * Lead ...

The Quality Manager will provide technical leadership within the Quality discipline, driving ... In-depth knowledge regulatory requirements for Medical, Pharmaceutical and Food packaging products ...

Showing results 41-60

Pharmaceutical Quality Manager information

See salary details

$24K

$86.2K

$158K

How much do pharmaceutical quality manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for pharmaceutical quality manager 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 pharmaceutical quality manager do?

A Pharmaceutical Quality Manager oversees the quality assurance and control processes within pharmaceutical manufacturing. They ensure that all products comply with regulatory standards, company policies, and industry best practices. Their responsibilities include developing quality management systems, conducting audits, and coordinating with production teams to resolve quality issues. Ultimately, they play a crucial role in maintaining product safety and efficacy for consumers.

What are some common challenges faced by pharmaceutical quality managers, and how can they be addressed?

Pharmaceutical Quality Managers often face challenges such as keeping up with evolving regulatory requirements, managing cross-functional teams, and ensuring continuous compliance throughout manufacturing processes. Staying current with global regulations and fostering open communication between departments are crucial for success. Implementing robust quality management systems and investing in ongoing staff training can help address these challenges, ensuring product safety and regulatory adherence.

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

To thrive as a Pharmaceutical Quality Manager, you need a solid background in pharmaceutical sciences, regulatory compliance, and quality management systems, often supported by a relevant degree and experience in GMP environments. Familiarity with tools like LIMS, CAPA systems, and certifications such as Six Sigma or ISO 9001 are typically important. Attention to detail, problem-solving, and strong leadership skills help ensure effective oversight and continuous improvement. These competencies are crucial for maintaining product safety, regulatory compliance, and operational excellence in pharmaceutical manufacturing.

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

AspectPharmaceutical Quality ManagerQuality Assurance Specialist
CredentialsTypically requires a Bachelor's degree in Pharmacy, Chemistry, or related field; often holds certifications like ASQ CQE or ISO auditorUsually holds a Bachelor's degree in Life Sciences or related; may also have certifications like ASQ CQPA or ISO auditor
Work EnvironmentManages quality teams, oversees quality systems, and ensures compliance across manufacturing facilitiesPerforms audits, reviews documentation, and supports quality processes within labs or production lines
Employer & Industry UsageCommonly employed in pharmaceutical manufacturing, biotech, and healthcare companiesFound in pharmaceutical, biotech, and medical device industries, often within quality departments

The Pharmaceutical Quality Manager focuses on leading quality management systems and strategic oversight, while the Quality Assurance Specialist handles day-to-day quality checks and documentation. Both roles are essential for ensuring product compliance and safety in the pharmaceutical industry.

More about Pharmaceutical Quality Manager jobs

What cities are hiring for Pharmaceutical Quality Manager jobs?

Cities with the most Pharmaceutical Quality Manager job openings:

What states have the most Pharmaceutical Quality Manager jobs?

States with the most job openings for Pharmaceutical Quality Manager jobs include:

Infographic showing various Pharmaceutical Quality Manager 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 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

Quality Manager

aspensurgical

Jamaica, NY โ€ข On-site

Full-time

Posted 4 days ago


Job description

In This Position, You Will Have the Opportunity To:

  • Serve as the Quality Management Representative (QMR) for the manufacturing facility, including hosting third party audits and inspections, organizing and conducting periodic Management Reviews of the Quality System
  • Carry out leadership responsibilities in accordance with the organizationโ€™s policies and applicable laws which includes interviewing, hiring, developing and training employees; planning, assigning, and directing work; appraising performance; rewarding and coaching employees; addressing complaints and resolving problems
  • Ensure all required investigations (i.e. complaints, NCs) are robust, thorough, and completed in a timely manner
  • Champion and lead continuous improvement, VIP, and standard work efforts
  • Chair the siteโ€™s Corrective Action Board (CAB) and drive the CAPA program by ensuring opportunities are well documented, timelines are adhered to and status is reported to management on a routine basis
  • Oversee activities associated with calibration of Inspection, Measure, and Test Equipment (IM&TE) including standards, recall, review/approval of records, and out of tolerance investigations
  • Lead, maintain and create efficiencies in the Quality Management System to fulfill both domestic and international quality system requirements (e.g. FDAโ€™s QMSR, ISO 13485, and other international standards)
  • Host FDA/ISO and other regulatory agencies or customers for audits
  • Support product integrations associated with acquisitions and new product development
  • Ensure the effective maintenance of Device History Records, and other quality documents
  • Manage the internal audit program including training internal auditors, creating and maintaining internal audit schedules, assuring internal audits are performed and completed according to approved schedule
  • Monitor the health and well-being of the QMS through quality trending, analytics and established KPIs

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What You Need to Succeed in This Position

  • Bachelorโ€™s Degree in Engineering or a related technical discipline such as, Chemistry or Biology.
  • A minimum of 5-8 years of quality assurance experience in a medical device, pharmaceutical, or regulated manufacturing environment.
  • A minimum of 1-3 yearsโ€™ experience managing quality team members.
  • Industry or discipline specific certification a plus (CQE, CQA, CMQ/OE, Lean, Six Sigma, etc)
  • Experience in chemical mixing, liquid formulation, or filling operations preferred.
  • Displays developed interpersonal skills: leadership, team orientation, ability to communicate at all levels
  • Ability to make effective decisions and maintain effectiveness under changing circumstances and priorities
  • Teamwork, communication, positive attitude required to support the manufacturing environment
  • Extensive experience in problem solving โ€“ able to perform root cause analysis and implement effective corrective actionsย ย 
  • Able to effectively manage and complete multiple projects simultaneously
  • Excellent computer skills including but not limited to Microsoft Office Suite
  • Knowledge of quality systems including the quality manual, quality policy and applicable procedures and work instructionsย 
  • Ability to support the establishment, implementation, and maintenance of the quality system in accordance to FDA Quality Management System Regulation, ISO 13485, and European Union Medical Device Directives.

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We're proud to be an equal opportunity employer- and celebrate our employees' differences, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or Veteran status.

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