ZipRecruiter

Log In

1

Pharmaceutical Quality Manager Jobs (NOW HIRING)

Phlow Corp

Pharmaceutical Quality Specialist

Petersburg, VA · On-site

$60K - $70K/yr

The Pharmaceutical Quality Specialist is responsible for overseeing and managing documentation and processes essential for qualification activities related to pharmaceutical manufacturing and quality ...

New

Phlow Corp

Pharmaceutical Quality Specialist

Petersburg, VA · On-site

$60K - $70K/yr

Description The Pharmaceutical Quality Specialist is responsible for overseeing and managing documentation and processes essential for qualification activities related to pharmaceutical manufacturing ...

New

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 ...

Lonza

Quality Assurance Manager

Bend, OR · On-site

Join our growing Quality team in Bend, Oregon as a QA Manager ... In this leadership role, you will help ensure commercial pharmaceutical products meet regulatory ...

Lonza

Quality Assurance Manager

Bend, OR · On-site

Join our growing Quality team in Bend, Oregon as a QA Manager ... In this leadership role, you will help ensure commercial pharmaceutical products meet regulatory ...

Mettler Toledo AG

Quality Manager

Plainsboro, NJ · On-site

Owning and improving the Quality Management System (QMS), ensuring compliance with ISO standards ... Innovation is at the core of all pharmaceutical, biopharma and bioprocess applications. With ...

next page

Showing results 1-20

All JobsScience JobsResearch JobsScientist JobsPharmaceutical Quality Manager Jobs

Pharmaceutical Quality Manager information

See salary details

$24K

$86.2K

$158K

How much do pharmaceutical quality manager jobs pay per year?

As of Sep 13, 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:

What are popular job titles related to Pharmaceutical Quality Manager jobs?

For Pharmaceutical Quality Manager jobs, the most frequently searched job titles are:

Pharmaceutical Quality Manager jobs near you
Infographic showing various Pharmaceutical Quality Manager job openings in the United States as of September 2026, with employment types broken down into 2% As Needed, 80% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 83% Physical, 1% Hybrid, and 16% Remote job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

Compounding Pharmaceutical QA/QC

Lake Charles, LA • On-site

VIDRINE PHARMACEUTICAL GROUP LLC
See more jobs at VIDRINE PHARMACEUTICAL GROUP LLCexternal

$75K - $85K/yr

Other

Re-posted 10 days ago

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Compounding Pharmaceutical QA/QC

Lake Charles, LA, US

3 days ago Requisition ID: 1133

Salary Range: $75,000.00 To $85,000.00 Annually

About the Role:

The Compounding Pharmaceutical Quality Assurance professional plays a critical role in ensuring that compounded medications meet the highest standards of safety, efficacy, and regulatory compliance. This position is responsible for overseeing and implementing quality assurance protocols throughout the compounding process, from raw material inspection to final product release. The role requires meticulous attention to detail to identify and mitigate risks, ensuring that all compounded pharmaceuticals adhere to applicable guidelines and industry best practices. The successful candidate will collaborate closely with compounding pharmacists, production teams, and regulatory bodies to maintain continuous quality improvement. Ultimately, this role safeguards patient health by guaranteeing that compounded medications are consistently produced to exacting quality standards.

Minimum Qualifications:

  • Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related scientific discipline.
  • Minimum of 3 years of experience in pharmaceutical compounding quality assurance or a closely related field.
  • In-depth knowledge of USP <795>, USP <797>, USP <800>, and FDA regulations applicable to pharmaceutical compounding.
  • Strong understanding of Good Manufacturing Practices (GMP) and quality management systems.
  • Proven ability to conduct audits, manage documentation, and implement quality control measures.

Preferred Qualifications:

  • Certification in Quality Assurance (e.g., ASQ Certified Quality Auditor or equivalent).
  • Experience working in a sterile compounding environment.
  • Familiarity with electronic quality management systems (eQMS) and laboratory information management systems (LIMS).
  • Advanced degree (Master’s or PharmD) in a relevant field.
  • Experience with risk assessment methodologies and root cause analysis.

Responsibilities:

  • Develop, implement, and maintain quality assurance procedures and documentation specific to pharmaceutical compounding operations.
  • Conduct regular audits and inspections of compounding processes, equipment, and facilities to ensure compliance with USP <795>, <797>, and other relevant standards.
  • Review and approve batch records, compounding formulas, and quality control test results prior to product release.
  • Investigate deviations, non-conformances, and complaints related to compounded products, and coordinate corrective and preventive actions.
  • Train and support compounding staff on quality assurance policies, regulatory requirements, and best practices to promote a culture of quality and compliance.

Skills:

The required skills enable the professional to rigorously evaluate compounding processes and ensure compliance with regulatory standards, which is essential for maintaining product quality and patient safety. Strong analytical and problem-solving skills are used daily to investigate deviations and implement effective corrective actions. Communication skills are vital for training staff and collaborating with cross-functional teams to foster a quality-driven environment. Attention to detail ensures accurate documentation and thorough audits, preventing errors and regulatory non-compliance. Preferred skills such as proficiency with electronic quality management systems enhance efficiency and accuracy in quality assurance activities, while advanced certifications and experience support continuous improvement initiatives.

#J-18808-Ljbffr

Apply