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Director Quality Operations Jobs (NOW HIRING)

SaniSure LLC

Director of Quality Operations

Camarillo, CA · On-site

$170K - $190K/yr

Job Summary The Director, Quality Operations is responsible for management and continuous improvement of Plant Quality Systems including customer and internal corrective/preventive actions and ...

Jj

Quality Operations Manager

Cornelia, GA · On-site

Planning, coordinating, and directing quality assurance programs designed to ensure continuous production of products consistent with established standards * Serving as the Quality Operations Site ...

Nurix

Senior Manager, Quality Operations

Brisbane, CA · On-site

Senior Manager, Quality Operations Nurix Therapeutics is a clinical-stage biopharmaceutical company ... Reporting to the Senior Director, Quality, the Senior Manager will execute essential quality ...

STERIS Corporation

Director, Quality

Mentor, OH · On-site

Position Summary The Director, Quality is responsible for leading multiple manufacturing/service ... Assures that local sites maintain and improve operational and quality systems to remain in a state ...

Steris Corporation

Director, Quality

Mentor, OH · On-site

Position Summary The Director, Quality is responsible for leading multiple manufacturing/service ... Assures that local sites maintain and improve operational and quality systems to remain in a state ...

Endo International

Sr. Director, Quality

Hobart, NY · On-site

The Sr. Director leads and mentors quality assurance and quality control teams, oversees daily quality operations, and serves as a key partner to site leadership by providing guidance on quality and ...

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Director Quality Operations information

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$34K

$107.7K

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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, Quality Operations and Quality Control

Veranova L P

Devens, MA • On-site

Full-time

Medical, Retirement, PTO

Posted 3 days ago

Job description

Director, Quality Operations and Quality Control

Discover Veranova

At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference. Every role at Veranova plays a part in delivering an exceptional customer experience through ownership and integrity.

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.

Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.

Role Overview

The Director, Quality Operations and Quality Control leads the Quality Operations function and Quality Control test labs for the Veranova sites located in Devens, MA and North Andover, MA. In collaboration with site Leadership, it is the responsibility of this role to ensure the day to day Quality Assurance aspects of manufacturing, testing, reporting, issue resolution and batch disposition of active pharmaceutical ingredients, intermediates meet the compliance requirements applicable to drug substance manufacturing of pharmaceutical products.

This position is fully onsite first shift at our Devens, MA facility.

Responsibilities
  • Aids in the creation of the Quality Operations (QO) and Quality Control (QC) strategy and implementation of the strategy at the site; Creates QC/QA workload planning, contributes to site budgeting, headcount and resource loading based on required skill sets and available assets
  • Assures the standards and QO oversight of batch production monitoring, quality control and release requirements are executed to ensure batch compliance with GMPs and regulatory filings. Including stopping manufacture or distribution of a product if necessary.
  • Leads or advises on root cause analysis performed to investigate manufacturing deviations, critical events, customer complaints, audit findings related to production or trends in quality metrics; Ensures compliance with QMS during production and testing including investigations, CAPA and Change Management.
  • Support implementation and execution of LIMS, TrackWise improvements and other E-systems projects.
  • In collaboration with Regulatory Affiars and QC, manage stability programs to support commercial products as well as new submissions, according to the ICH guidelines and zone requirements; Develop, improve, and revise Standard Operating Procedures testing monographs; Monitors documentation practices to assess data integrity during the production, testing, review of products for clinical or commercial use; Actively engages or leads teams in product or process/product technology transfers and method transfers across sites.
  • In collaboration with site VP/GM, presents Quality Performance metrics to Executive leadership during quarterly management review meetings; Engages with site teams to review Quality Performance metrics and recommend actions for continuous improvement; Participate in Site leadership team to execute overall business priorities; Manages, coaches and develops site Quality team members for the purpose of both professional development and succession planning
  • Engages with peer across regions to coordinate/harmonize product monitoring and disposition requirements as well as evaluate investigation trends and audit findings within and across sites to facilitates team discussion on proper global CAPA.
  • Assures proper execution of process, product and method validation through review, guidance and approval of protocols and final reports verifying compliance with regulatory expectations; Oversees the QC laboratory and interacts with production floor operations which require safety training and proper use of PPE applicable to the facility and operation.
  • Engages and leads discussions with customers as needed to resolve complaint issues, audit observations, or quality agreement terms; Leads the sites during Regulatory Agency Inspections and customer audits. Assists with DEA compliance requests as needed.
  • Responsible for the Quality execution which requires intermittent travel within the region and periodically across sites for engagement with peers, site functional leaders, customers and strategy meetings.
  • Carries out any other duties within the employee’s skills and abilities whenever reasonably

Qualifications:

  • BS or equivalent in Chemistry or related Science
  • 15+ years experience within GMP Quality Assurance and Quality Control in an FDA/EMA regulated industry; 10+ years directly managing performance and development of staff members
  • 7+ years experience with batch production, control and disposition processes and QC Laboratory testing
  • Expert knowledge in Root Cause Analysis, Investigations, CAPA and CAPA Effectiveness; Familiarity with Veeva, Master Control, LIMS and ERP systems; Experience within Drug substance manufacturing; Working knowledge of US & EU GMP, ICH Q7 and Part 11 compliance
  • Expert knowledge in process validation, production equipment qualification, environmental controls, and change management; Experience with customer complaint investigations
  • Knowledge of basic microbiology and contamination control as they apply to drug substance manufacturing, specifically bioconjugation operations
  • Ability to Plan, Organize, Prioritize and Monitor workload across multiple sites and customer projects; Familiarity with risk management principles and capable of decision making based on risk management; Ability to independently interact with customers, vendors, and regulatory inspectorates
  • Familiarity with project management and ability to lead improvement projects across multiple sites
  • Strong experience with Microsoft Office applications, including Word, Excel and PowerPoint

Salary Range: $190,000-$210,000 annual base salary.

The salary range for this role is $190,000–$210,000. This range represents a good‑faith estimate of the compensation we expect to offer for this position at the time of posting. Actual compensation will be based on factors such as relevant experience, skills, qualifications, and internal equity. In exceptional cases, compensation may exceed the stated range.

All full-time employees are eligible to participate in our annual incentive bonus program. Bonus targets vary by career level and are based on individual and company performance.

Our Commitment:

  • Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
  • Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.
  • Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.
  • Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don’t meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.

How to Apply:

At Veranova, we are on a mission to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit www.veranova.com to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise.

We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed.

Additional Information:

Applicants for this role must be authorized to work in the United States without further employer sponsorship.

Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.

All your information will be kept confidential according to EEO guidelines.

Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.

All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

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