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Quality Assurance Manager Pharmaceutical Jobs (NOW HIRING)

CorDx

Quality Assurance Manager

Alpharetta, GA

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

company372

Quality Assurance Manager

Madison, WI · On-site

The QA Manager requires the ability to evaluate, investigate, solve problems, and respond to ... A minimum of 4-5 years in GMP quality assurance or compliance within the pharmaceutical or biotech ...

CorDx

Quality Assurance Manager

Chamblee, GA · On-site

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

CorDx

Quality Assurance Manager

Chamblee, GA · On-site

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

Focus Lab

Quality Assurance Manager

Cherry Hill, NJ · On-site

$110 - $150/hr

Scope of the Role The QA Manager leads TPM Laboratories' quality system and ensures laboratory work ... Bachelor's in Chemistry (or related discipline) * 6-8 years in a regulated pharmaceutical ...

Bimeda Inc.

QA Manager

Pomona, CA

Job Title: QA Manager (Quality Assurance) Location:Pomona, CA (In-office) Position Type:Full-time ... What We Are Looking For Required: * 5-7 years of experience in a regulated pharmaceutical industry ...

Bimeda Inc.

QA Manager

Pomona, CA · On-site

$122K - $149K/yr

Job Title: QA Manager (Quality Assurance) Location: Pomona, CA (In-office) Position Type: Full-time ... What We Are Looking For Required: * 5-7 years of experience in a regulated pharmaceutical industry ...

J.M. Murray Center, Inc.

Quality Assurance Mgr

Cortland, NY · On-site

$29.98 - $37.03/hr

GENERAL SUMMARY The Quality Assurance (QA) Manager is responsible for ensuring that medical devices and pharmaceutical products comply with applicable regulatory requirements, quality standards, and ...

New

J.M. Murray Center, Inc.

Quality Assurance Mgr

Cortland, NY · On-site

$29.98 - $37.03/hr

GENERAL SUMMARY The Quality Assurance (QA) Manager is responsible for ensuring that medical devices and pharmaceutical products comply with applicable regulatory requirements, quality standards, and ...

New

Sterigenics

Quality Assurance Manager

Marion, AR · On-site

$90 - $130/hr

... top 10 pharmaceutical companies.Reporting to the General Manager, the Quality Assurance (QA) ... Manager is directly responsible for managing and coordinating all quality functions for the ...

Granules

Quality Assurance Manager

Manassas, VA · On-site

The QA Manager ensures compliance with cGMP and internal policies, procedures and specifications ... the pharmaceutical manufacturing industry. · Writing and maintaining cGMP documentation. · ...

Kutol-Product

Quality Assurance Manager

Cincinnati, OH · On-site

$110 - $140/hr

As the Quality Assurance Manager, you will lead QA activities for our OTC drug and cosmetic ... Bachelor's degree in Chemistry, Microbiology, Biology, Pharmaceutical Sciences, Engineering, or a ...

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Quality Assurance Manager Pharmaceutical information

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How much do quality assurance manager pharmaceutical jobs pay per year?

As of Aug 30, 2026, the average yearly pay for quality assurance manager pharmaceutical 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 quality assurance manager do in the pharmaceutical industry?

A Quality Assurance Manager in the pharmaceutical industry is responsible for ensuring that all products meet strict quality and regulatory standards. They develop, implement, and maintain quality management systems, oversee audits and inspections, and ensure compliance with Good Manufacturing Practices (GMP). Their role includes managing documentation, training staff on quality protocols, and addressing any deviations or non-conformances to maintain product safety and efficacy.

What are some common challenges faced by a quality assurance manager in the pharmaceutical industry, and how can they be addressed?

Quality Assurance Managers in the pharmaceutical sector often encounter challenges such as maintaining compliance with evolving regulations, managing documentation for audits, and ensuring cross-departmental communication. Staying updated with regulatory changes and implementing robust training programs can help address compliance issues. Establishing clear documentation processes and fostering a culture of quality across teams are also key strategies to overcome these challenges. Regular collaboration with production, R&D, and regulatory affairs ensures consistency and alignment on quality standards.

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

To thrive as a Quality Assurance Manager in the pharmaceutical industry, you need a deep understanding of GMP regulations, quality systems, and a relevant science degree or equivalent experience. Familiarity with quality management software, regulatory databases, and certifications such as Six Sigma or ISO 9001 are typically important. Strong leadership, attention to detail, and effective communication skills help ensure compliance and foster a culture of quality. These competencies are crucial for maintaining product safety, meeting regulatory requirements, and supporting continuous improvement within pharmaceutical operations.

What is the difference between Quality Assurance Manager Pharmaceutical vs Quality Control Supervisor Pharmaceutical?

AspectQuality Assurance Manager PharmaceuticalQuality Control Supervisor Pharmaceutical
CredentialsTypically requires a degree in pharmacy, chemistry, or related field; certifications like ASQ CQE or CQA are commonRequires a degree in chemistry, biology, or related; certifications are less common but may include GMP training
Work EnvironmentOversees quality systems, audits, and compliance across departmentsSupervises laboratory testing and quality control processes
Employer & Industry UsageUsed in pharmaceutical manufacturing, regulatory compliance, and quality assurance departmentsFound in laboratories, manufacturing plants, and quality control labs

The Quality Assurance Manager Pharmaceutical focuses on establishing and maintaining quality systems, ensuring compliance, and managing audits. In contrast, the Quality Control Supervisor Pharmaceutical primarily oversees laboratory testing and quality control procedures. Both roles are essential in pharmaceutical quality management but differ in scope and responsibilities.

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Quality Assurance Manager Pharmaceutical jobs near you
Infographic showing various Quality Assurance Manager Pharmaceutical job openings in the United States as of August 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.

Quality Assurance Manager

Manassas, VA • On-site

Granules Pharmaceuticals
See more jobs at Granules Pharmaceuticalsexternal

Full-time

Re-posted 9 days ago

Job description

Job Type
Full-time
Description
*This is an Onsite Role**
The QA Manager ensures compliance with cGMP and internal policies, procedures and specifications. This position is responsible for performing documentation for all quality system functions in accordance with cGMP and related company SOP's, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines.
  • The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements.
  • Managing all quality operations to include inspection of components, bulk, and final products for the Manassas, VA, ensuring release lead times are met with timely product disposition.
  • Ensure that the facility is meeting all training requirements.
  • Lead the communication of open quality document notification and resolution between all departments regarding Complaints, Investigations, Change Control, CAPA's (including verification of CAPA's) and other quality documents as needed.
  • Manage and maintain audit inspections (Internal and External) for the site.
  • Responsible for supporting the preparation, review, processing, and approval of various validation documents as application for the Granules, Manassas, facility.
  • Provide QA support, review and approval for relevant documents including relevant procedures, batch records, specifications, stability reports, technical reports (i.e., Qualification, Validation, Transportation.), trend reports, Annual Product Quality Reviews and other documents as needed.
  • Responsible for performance and development of all Quality Assurance staff through mentoring and focusing on personal and professional growth.
  • Work with Quality leadership team for proactive succession planning and a high-performance culture through people.
  • Guide and lead by setting realistic personal goals for staff and provide regularly scheduled feedback throughout the year.
  • Provide the means for incorporating the necessary tools, equipment, and methods into the new and existing processes aimed at continuous improvement.
  • Implementation Quality management system tools and their compliance.
  • Development and execution of quality training modules for the organization.
  • Ensure staff receives appropriate knowledge and skill development and growth opportunities
  • Work with Regulatory Affairs to supply information needed for FDA filings.
  • Other duties as assigned by management.

Requirements
Knowledge & Skills
• Expert-level knowledge of the FDA guidance for Industry, Title 21 of the Code of Federal Regulations and Compendia (USP/EP/BP/etc...)
• cGMP compliance within the pharmaceutical manufacturing industry.
• Writing and maintaining cGMP documentation.
• Analyze data/information and resolve complex issues.
• Verbal and written communication skills.
• Work and communicate with cross-functional teams.
• Multiple priorities and re-prioritize tasks.
• Strong computer skills and working knowledge of Microsoft Office Suite and Adobe
• Demonstrated ability to work on complex assignments in collaboration with various departments.
Experience & Education
• Bachelor's degree in the life sciences (or equivalent work experience) minimum of 6+ years in a QA role within the pharmaceutical industry
• Master's degree with 4+ years of pharmaceutical manufacturing experience and at least 3 years of those years in a progressive challenging QA department in the pharmaceutical industry.
Physical Requirements/Working Environment
• While performing the duties of this job, the employee is regularly required to, stand, sit, talk, hear, and use hands and fingers to operate a computer and telephone keyboard.
• Specific vision abilities required by this job include close vision requirements due to computer work.
• Ability to sit at a computer terminal for an extended period of time.
• Light to moderate lifting up to 10-15 lbs is required.
• Ability to work in a confined area

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