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Pharmaceutical Quality Director Jobs (NOW HIRING)

Pinnaql

Quality Director

Tempe, AZ

We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Quality Director ABOUT THE ROLE The Quality Director leads the Quality organization and serves as ...

Pinnaql, Inc.

Quality Director

Tempe, AZ · On-site

We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Quality Director ABOUT THE ROLE The Quality Director leads the Quality organization and serves as ...

Pinnaql

Quality Director

Tempe, AZ · On-site

We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Quality Director ABOUT THE ROLE The Quality Director leads the Quality organization and serves as ...

Pinnaql

Quality Director

Tempe, AZ · On-site

We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Quality Director ABOUT THE ROLE The Quality Director leads the Quality organization and serves as ...

Pinnaql, Inc.

We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Quality Director ABOUT THE ROLE The Quality Director leads the Quality organization and serves as ...

Cosette Pharmaceuticals Inc.

Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with ... The Senior Director, Quality Operations will suppor t quality initiatives and ensure compliance ...

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Pharmaceutical Quality Director information

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$31K

$125.6K

$213.5K

How much do pharmaceutical quality director jobs pay per year?

As of Sep 12, 2026, the average yearly pay for pharmaceutical quality director in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What is the difference between Pharmaceutical Quality Director vs Pharmaceutical Quality Manager?

AspectPharmaceutical Quality DirectorPharmaceutical Quality Manager
ResponsibilitiesOversees entire quality systems, strategic planning, and compliance at a senior levelManages daily quality operations, implements quality procedures, and supervises quality staff
CredentialsTypically requires advanced degrees and extensive experience in quality assuranceRequires relevant experience and certifications like CQE or ISO auditor
Work EnvironmentExecutive-level, strategic, often involved in cross-departmental decisionsOperational, hands-on role within quality assurance or control departments

The Pharmaceutical Quality Director focuses on strategic leadership and overall quality system oversight, while the Pharmaceutical Quality Manager handles daily quality operations and team supervision. Both roles require strong quality credentials and industry experience, but differ mainly in scope and level of responsibility.

What cities are hiring for Pharmaceutical Quality Director jobs?

Cities with the most Pharmaceutical Quality Director job openings:

What are the most commonly searched types of Pharmaceutical Quality jobs?

The most popular types of Pharmaceutical Quality jobs are:

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

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

Infographic showing various Pharmaceutical Quality Director job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Pharmaceutical QA Director

Tustin, CA • On-site

Eliquent Life Sciences
See more jobs at Eliquent Life Sciencesexternal

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This job post has expired today. Applications are no longer accepted.

Job description

Pharmaceutical QA Director

The Pharmaceutical QA Director plays a critical leadership role in ensuring the highest standards of quality and compliance within pharmaceutical manufacturing operations. This position is responsible for overseeing all quality assurance activities, including departmental leadership, quality control, and process validation, to guarantee that products meet regulatory requirements and internal standards. The director will lead cross-functional teams to implement and maintain robust quality systems that support drug research projects and manufacturing processes. They will also serve as a key liaison with regulatory agencies, ensuring timely and successful audits and inspections. Ultimately, this role drives continuous improvement initiatives to enhance product quality, patient safety, and operational efficiency across the organization.

Minimum Qualifications:

  • Bachelor's degree in Pharmacy, Chemistry, Microbiology, or a related scientific discipline.
  • Minimum of 10 years of experience in pharmaceutical quality assurance, including at least 5 years in a leadership role.
  • Demonstrated expertise in departmental leadership, quality control, microbiology quality assurance, and process quality assurance within a pharmaceutical manufacturing environment.
  • Strong knowledge of FDA regulations, cGMP guidelines, and other relevant regulatory requirements.
  • Proven experience managing drug research project quality and successfully leading regulatory inspections.

Preferred Qualifications:

  • Advanced degree (Master's or PhD) in a relevant scientific field.
  • Certification in Quality Assurance (e.g., ASQ Certified Quality Auditor or Quality Manager).
  • Experience with global regulatory agencies such as EMA, PMDA, or Health Canada.
  • Familiarity with electronic quality management systems (eQMS) and data integrity principles.
  • Track record of implementing Lean or Six Sigma methodologies in quality assurance processes.

Responsibilities:

  • Lead and manage the Quality Assurance department, providing strategic direction and fostering a culture of quality and compliance.
  • Oversee quality control and quality assurance processes, including microbiology and process quality assurance activities, to ensure adherence to cGMP and other regulatory standards.
  • Manage and support drug research project quality requirements, ensuring that all phases of development comply with internal and external quality standards.
  • Coordinate and prepare for regulatory inspections and audits, addressing any findings with effective corrective and preventive actions.
  • Collaborate with manufacturing, research, and regulatory teams to develop and implement quality systems, policies, and procedures that support continuous improvement.

Skills:

The required skills are integral to the daily responsibilities of the Pharmaceutical QA Director. Departmental leadership skills enable the director to effectively manage and inspire quality teams, ensuring alignment with organizational goals. Drug research project management skills are essential for overseeing quality aspects throughout the drug development lifecycle, ensuring compliance and risk mitigation. Quality control and microbiology quality assurance skills are applied to monitor and validate manufacturing processes, guaranteeing product safety and efficacy. Process quality assurance expertise supports the continuous evaluation and improvement of production workflows, while preferred skills such as regulatory knowledge and quality certifications enhance the director's ability to navigate complex compliance landscapes and drive operational excellence.

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