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Director Quality Operations Jobs (NOW HIRING)

AAON, Inc.

Director, Quality

Longview, TX · On-site

The Director partners closely with Operations, Supply Chain, and cross-functional leaders and drive a proactive quality culture. Primary Duties * Lead all quality performance for the Business Unit ...

Abbott

Director, Quality

Sylmar, CA · On-site

$172K - $344K/yr

Translate quality strategy into execution, driving first-time quality, operational excellence, and ... Direct work with FDA and other geographic regulators to enable continued good standing of the CRM ...

AMRI

Director, Quality Remediation

Albany, NY · On-site

Director, Quality Remediation Build your future at Curia, where our work has the power to save ... Experience in Sterile, API and Biologics Products Quality Operations is preferred Knowledge, skills ...

Catalent, Inc.

Director, Quality

Kansas City, MO · On-site

... Safety, Quality Performance, Operational Excellence, Continuous Improvement, Error Reduction ... Direct experience and working knowledge of Validation principles, including validation of processes ...

Generac

Director Quality

East Peoria, IL

$156K - $215K/yr

The Quality Director is accountable for leading and continuously improvingbusinessgroupwidequality ... The position partners closely withcrossfunctionalleaders across Operations, Engineering, Field ...

AAON, Inc.

Director, Quality

Longview, TX

The Director partners closely with Operations, Supply Chain, and cross-functional leaders and drive a proactive quality culture. Primary Duties * Lead all quality performance for the Business Unit ...

Curia, Inc.

Director, Quality Remediation

Albany, NY · On-site +1

Director, Quality Remediation Build your future at Curia, where our work has the power to save ... Experience in Sterile, API and Biologics Products Quality Operations is preferred Knowledge, skills ...

WVU Medicine

Director Quality

Buckhannon, WV · On-site

Responsible for directing the overall operation of departments and clinical areas which may include: Quality, Infection Control, Regulatory, Patient and Employee Safety, Risk Management, and/or ...

Lifepoint Health

Director, Quality

Madison, WI · On-site

Direct the hospital-wide CQPI operations, including record reviews for quality indicators and reporting findings to leadership, Medical Executive Committee, Board of Managers, and other committees.

Lifepoint Health

Director, Quality

Madison, WI · On-site

Direct the hospital-wide CQPI operations, including record reviews for quality indicators and reporting findings to leadership, Medical Executive Committee, Board of Managers, and other committees.

Itron, Inc

Director Quality

West Union, SC

Itron is seeking a Director, Global Manufacturing Quality ... Reporting to the Vice President of Global Quality, this executive will lead operational execution ...

Dover Corporation

Director, Quality

Austin, TX

The Director of Quality, Mfg. & Supply Chain will report to the VP of Operations for North America. This position will be based from our Austin-Texas headquarters and will require some national ...

Globus Medical

Director, Quality

Audubon, PA · On-site

Position Summary: The Director of Quality provides strategic leadership and oversight of the ... International Operations Quality * Oversee quality system compliance at all international ...

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How much do director quality operations jobs pay per year?

As of Jun 20, 2026, the average yearly pay for director quality operations in the United States is $107,680.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $135,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director of Quality Operations, and why are they important?

To thrive as a Director of Quality Operations, you need expertise in quality management systems, regulatory compliance, and process improvement, often supported by a relevant degree and extensive experience in quality assurance. Familiarity with tools such as Six Sigma, ISO standards, and quality management software is typically required, along with certifications like ASQ Certified Manager of Quality/Organizational Excellence (CMQ/OE). Strong leadership, strategic thinking, and effective communication are vital soft skills for driving cross-functional initiatives and fostering a culture of continuous improvement. These skills ensure that organizational processes meet regulatory standards, reduce risk, and support business objectives.

Is a director of operations higher than a general manager?

A Director of Quality Operations is typically a higher-level leadership role than a General Manager, overseeing multiple departments or business units and setting strategic goals. While a General Manager manages daily operations within a specific area, the director often has broader responsibilities and reports to executive leadership. The hierarchy can vary by organization, but generally, the director position is senior to a general manager.

What jobs pay 500,000 a year in the US?

High-level executive roles such as Chief Executive Officers, Chief Financial Officers, and other C-suite positions often have annual compensation exceeding $500,000, especially in large corporations. Additionally, specialized roles like certain surgeons, investment bankers, and successful entrepreneurs can reach or surpass this income level, often requiring advanced skills, extensive experience, and significant responsibility.

What are the main challenges a Director of Quality Operations typically faces when coordinating cross-functional teams?

Directors of Quality Operations often encounter the challenge of aligning diverse teams—such as manufacturing, regulatory, and R&D—toward shared quality goals. Balancing differing priorities, managing communication across departments, and ensuring consistent adherence to quality standards can be complex. Effective leaders in this role foster collaboration, establish clear processes, and proactively address potential bottlenecks to drive continuous improvement and compliance. Developing strong interpersonal relationships and maintaining transparency are crucial to successfully navigating these challenges.

What does a Director of Quality Operations do?

A Director of Quality Operations oversees the quality assurance and control processes within an organization, ensuring that products or services meet established standards. They develop and implement quality management systems, lead compliance initiatives, and coordinate cross-functional teams to improve operational efficiency. This role often involves monitoring regulatory requirements, managing audits, and driving continuous improvement projects. The Director of Quality Operations plays a key leadership role in maintaining customer satisfaction and supporting business objectives.

What jobs make around $100,000 a year?

For a Director of Quality Operations, annual salaries around $100,000 are common, especially with experience, certifications, and leadership responsibilities. Other roles in management, engineering, IT, and healthcare also often reach or exceed this salary level, depending on industry and location.

How much does a QA director make in the US?

A Quality Assurance (QA) Director in the US typically earns between $100,000 and $160,000 annually, depending on experience, industry, and location. Senior roles with extensive experience and certifications can earn higher salaries, often exceeding $180,000. Compensation may also include bonuses and benefits related to leadership and quality management skills.
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Director Quality Operations jobs near you
Infographic showing various Director Quality Operations job openings in the United States as of June 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $107,680 per year, or $51.8 per hour.

Director of Quality

Piramal Pharma Limited

Sellersville, PA • On-site

Full-time

Posted yesterday

Job description

Be the First to Apply
Division
Piramal Pharma Solutions
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.
This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.
Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.
For more details, please visit : www.piramalpharmasolutions.com
Job Title
Director of Quality
Job Description
Director of Quality & Regulatory Affairs
Director, Quality & Regulatory Affairs
Job Description
The Director, Quality & Regulatory Affairs will maintain Sellersville Quality procedures and systems to ensure regulatory compliance. The incumbent will be an integral member of the Senior Leadership Team. The Director of Quality Operations is responsible for the quality unit at the site and for oversight of all quality related activities at the site. The site quality head is responsible to ensure that the systems, procedures and practices at the site comply with Piramal policies and the requirements of all major regulatory body agencies (e.g. FDA/Health Canada/EMA, etc).
Key accountabilities:
  • Management and Leadership: Leads the Quality Assurance, Quality Control, Stability and related site quality activities, including commercial and development products.
  • Release or reject API: Maintain decision making authority and maintenance of systems to release or reject API, intermediates, starting materials, raw materials, processing aids, packaging components, and labeling; Oversee system to ensure materials are produced and tested in a manner consistent with the applicable regulatory findings; Ensure that ancillary documentation including cleaning records, environmental monitoring records, calibration records, etc. are appropriately reviewed and approved by QA; Oversee system for preparing Certificates of Analysis, Certificates of Conformance, Summaries of Test Results, BSE/TSE Certification, and Approved Labelling, as required by client
  • Release or reject Batches: Works with the QC team to ensure the availability of materials necessary to meet the site's targeted number of API batch releases.
  • Works with the QA team to ensure the timely completion of investigation, batch record reviews and batch releases to meet the site's monthly targeted batch releases.
  • Inspections and Audits: Assume lead role in regulatory inspections and client audits, prepare responses to audit findings, direct implementation of corrective and preventative actions (CAPAs); lead PPS-Sellersville's internal audit program, schedule audits, prepare reports, direct implementation of CAPAs; lead PPS-Sellersville's external audit program, schedule audits, prepare reports, monitor contractor/supplier implementation of CAPAs; participate in implementation of quality agreements with clients, contractors, and suppliers.
  • Provide clear direction to achieve business goals, creating an environment that fosters team commitment and employee engagement such that revenue and expenditure targets are consistently met.
  • Maintain the perseverance to drive and sustain the changes that occur at the site, while being resilient and flexible, and inspiring and motivating the team.
  • Constantly communicates to the team, is open to opinions and feedback from team members and follows through on commitments.
  • Creates a work environment in which people are able to perform to the best of their abilities.
  • Through various strategic initiatives drive cost control and cost reduction. Responsible for working to develop and comply with the Quality budget.
  • Investigations, Corrective Action/Preventative Action: Review and/or approve deviations, out-of-specification reports, formal investigations, complaint investigations; Corrective Action/Preventative Action (CAPA) program and other reports as necessary.
  • Training: Responsible for the overall employee training and skills assessment for the site. Ensures the site is supported by sufficient adequately experienced, trained and equipped quality management and staff to control and assure the purity, efficacy, quality and strength of product manufactured at the site. Coaches, councils and mentors staff on issues relating to job activities and career development.
  • Records and Reports: Ensure appropriate level of quality assurance review and approval for the following protocols and associated reports: process validation, cleaning validation, analytical method validation, equipment/utilities qualification and stability; prepare reports related to equipment, processing, or testing, as requested by the client; prepare, review, and/or approve Annual Product Reviews.
  • Procedure preparation, review, and approval: Prepare, edit, review, and/or approve Standard Operation Procedures administering the Quality System; Ensure appropriate level of quality assurance review and approval for all master production procedures, specifications, and analytical test methods; ensure appropriate level of quality assurance review and approval for all procedures affecting the quality of intermediates or APIs; evaluate changes that may affect API quality and either approve or reject proposed changes (Change Control).
  • Regulatory Responsibilities: Work with Regulatory Affairs Manager to provide Regulatory and CMC support for clients including the preparation of documents for submission to USFDA, including Drug Master Files and Common Technical Documents; maintaining existing submissions with annual updates; and coordinating the preparation of responses to agency questions regarding these applications. Maintain all necessary regulatory licenses for site to continue operations.

Key competencies:
  • Highly motivated self-starter that can work, and lead, with minimal supervision.
  • Demonstrated ability to identify improvement areas and implement solutions to streamline process, communication, training and consistency.
  • Extensive knowledge of GMP requirements (21CFR Part 211 and/or ICH Q7).
  • Knowledge of Drug Regulatory requirements, specifically as relates to preparation of CMCs, DMFs or CTDs.
  • Knowledge of Lean Manufacturing, Six Sigma and team problem solving.
  • Knowledge of other industry guidance documents (such as ISPE Bulk Pharmaceutical Guide, GAMP 5).
  • Thorough knowledge of, and capability within, various Quality Management Systems.
  • Proven change management and leadership skills.
  • Excellent organizational and planning skills.
  • Strong written, verbal, and interpersonal communication skills.
  • Have the ability to develop, perform, evaluate, and troubleshoot within a scientific discipline.
  • Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines

Qualifications
  • Bachelor's degree in the physical sciences or engineering; advanced scientific degree strongly preferred. Education Preferred MS or Ph.D. in scientific or healthcare discipline or equivalent combination of education and related experience.
  • 15+ years' Pharmaceutical or Biotechnology QA and Regulatory experience, with demonstrated growth in responsibilities and expertise.
  • 7+ years' experience managing all aspects of a Quality department and function.
  • Significant work experience in a CMO and drug development environment.
  • Demonstrated knowledge and experience in supporting a team and Quality practices in a high-growth environment.
  • Detailed knowledge of chemistry and manufacturing controls

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