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Pharmaceutical Quality Manager Jobs (NOW HIRING)

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX · On-site

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced ... The QA Specialist will be responsible for implementing and maintaining quality management systems ...

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX · On-site

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced ... The QA Specialist will be responsible for implementing and maintaining quality management systems ...

Medix

Quality Manager

Deerfield, IL · On-site

$50 - $65/hr

The role involves managing regulatory intelligence activities, supporting document control ... Prior experience in pharmaceutical quality systems and proficiency with Veeva are essential.

Shionogi Inc.

QA Product Manager

Florham Park, NJ

Overview The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...

Shionogi Inc.

QA Product Manager

Florham Park, NJ · On-site

The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...

Shionogi Inc.

QA Product Manager

Florham Park, NJ · On-site

Overview The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...

ORGANIC POAG LLC

Quality Manager

Little Rock, AR · On-site

Join My Medical Supply, a leading pharmaceutical warehouse distribution facility committed to ... We are seeking a dedicated and detail-oriented Quality Manager to oversee our quality assurance ...

Stryker

Associate Quality Manager, Stability

Cary, IL · On-site

$112K - $188K/yr

Deep expertise in pharmaceutical stability testing aligned with ICH and global regulatory standards, supported by comprehensive knowledge of diverse analytical techniques and instrumentation.

Futran Tech Solutions Pvt. Ltd.

Quality Manager

The position works closely with Medical Directors, Pharmacists, data analytics and the care ... Work with Quality Care Managers on overarching goals and best practices from multiple contracts

Stryker

Associate Quality Manager, Stability

Cary, IL · On-site

$112K - $188K/yr

Deep expertise in pharmaceutical stability testing aligned with ICH and global regulatory standards, supported by comprehensive knowledge of diverse analytical techniques and instrumentation.

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Pharmaceutical Quality Manager information

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$24K

$86.2K

$158K

How much do pharmaceutical quality manager jobs pay per year?

As of Jul 15, 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 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.

How much does a QA manager make at Novartis?

A Pharmaceutical Quality Manager at Novartis typically earns between $100,000 and $130,000 annually, depending on experience, location, and certifications. The role involves overseeing quality assurance processes, ensuring compliance with regulatory standards, and managing quality teams in a pharmaceutical manufacturing environment.

What is the salary of a QA manager?

The salary of a Pharmaceutical Quality Manager typically ranges from $80,000 to $130,000 annually, depending on experience, location, and company size. They often hold certifications such as Six Sigma or GMP knowledge and oversee quality assurance processes in pharmaceutical manufacturing environments.

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 role of a pharmaceutical quality manager?

A pharmaceutical quality manager oversees the quality assurance and control processes in pharmaceutical manufacturing to ensure products meet regulatory standards and company specifications. They develop and implement quality systems, conduct audits, and collaborate with regulatory agencies, often requiring knowledge of Good Manufacturing Practices (GMP) and relevant certifications. Their role is essential for maintaining product safety, efficacy, and compliance throughout the production cycle.

What is the highest salary in QA Pharma?

The highest salary for a Pharmaceutical Quality Manager can reach up to $150,000 or more annually, depending on experience, location, and company size. Senior professionals with extensive expertise and certifications such as CQE or CQA tend to earn the top salaries in this field.

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.
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What job categories do people searching Pharmaceutical Quality Manager jobs look for? The top searched job categories for Pharmaceutical Quality Manager jobs are:
Pharmaceutical Quality Manager jobs near you
Infographic showing various Pharmaceutical Quality Manager 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 $86,159 per year, or $41.4 per hour.
Pharmaceutical Quality Associate

Pharmaceutical Quality Associate

FIRST PRIORITY, INC

Elgin, IL

$20 - $25/hr

Other

Posted yesterday

New

Job description

Description

GENERAL SUMMARY:


A member of the Quality Assurance (QA) team for a veterinary pharmaceutical manufacturing company. Responsible for coordinating, preparation and issuance of all manufacturing, packaging and testing documents for scheduled production and for maintenance of the Master Batch Records. Responsible for the review of all in process and finished product lot documentation to ensure compliance with cGMP, SOP and FDA regulations for release of product. Responsible for data entry and trending of all in process, finished product and manufacturing data per product for use in investigations, monthly management reviews, annual product reviews. To provide recommendations, resolutions and take appropriate action to ensure compliance. As required, backs up QA line personnel performing quality checks and documentation review.


PRIMARY RESPONSIBILITIES:

  • Determines and selects appropriate master documents, test specification and worksheets for assembly and preparation of complete and accurate production batch records. 
  • Calculates and assigns expiration date for each scheduled product.
  • Administers the issuance of all necessary documents for each scheduled product; assures and verifies critical information such as lot number and expiration date.
  • Develops appropriate batch records to meet the documentation requirements of validation protocols, special studies, and component qualification.
  • Performs thorough review of production batch records, cleaning, laboratory testing documentation, etc. and forwards production batches to the QA Supervisor for final release ensuring release timelines are met. 
  • Works with Operations and Quality personnel to correct identified deficiencies to ensure timely release of batches.
  • Generates Certificates of Analysis and Compliance for each production lot. 
  • Generates Minitab Charts for In-Process and Finished Product using Minitab Statistical Software.
  • Reviews and releases incoming raw materials.
  • Tracks batch release performance metrics and provide to compliance for inclusion in management review meetings and product reviews. 
  • Assists in the review and revision of SOPs, protocols, and special studies required for compliance with batch records.
  • Ensures all batch record and specification sheet maintenance, issuance, revision, and review SOPs remain compliant with FDA expectations and reflect current First Priority practices.
  • Controls and maintains the current files for all master batch records, test methods, and specification sheets required for manufacturing, packaging, and testing.
  • Performs API calculations per the batch record requirements.
  • Issue OOS No., NIDR No, QA Hold Notification and maintain electronic log and logbook.
  • Reviews Brite Stock packets. 
  • Assists, as needed, performing QA Specialist tasks on manufacturing lines. 
  • Assists in Label Room as necessary. 
  • Leads special projects as requested by management. 

Requirements

QUALIFICATIONS:


Education and/or Experience:

  • Bachelor's Degree with 0-2 years' work experience or High School degree with 4+ years' experience in pharmaceutical quality with experience in documentation review.
  • Basic knowledge of Microsoft Office (Word, PowerPoint, Excel, Outlook) required.

TRAINING:


On the job training:

  • Good Manufacturing Practices (GMP)
  • Quality Assurance Procedures

WORK ENVIRONMENT:

  • Office environment
  • Occasional work in light manufacturing environment
  • Working independently with minimal supervision
  • Low to medium noise level
  • Temperature controlled environment

TOOLS AND EQUIPMENT:

  • Microsoft Office
  • Quality Management Systems Program
  • Copy Machine
  • Calculator

Please note this job posting is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.


FLSA: Non-Exempt

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