Director, Quality

Catalent Pharma Solutions; Princeton (NJ); On-site; USD 190,000 - 230,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

Tuition reimbursement

PTO and holidays

Career growth opportunities

Job summary

Catalent Pharma Solutions in Princeton, NJ is seeking a Director of Quality to set strategic direction for quality, ensure staffing, and maintain the Quality Management System to meet regulatory and customer requirements. You will lead site metrics, management reviews, and oversee QA/QC with responsibility for batch disposition, while collaborating with customers to resolve quality concerns.

The role requires extensive cGMP/ICH knowledge, strong leadership, and a track record of guiding large

Qualifications

• Bachelor’s degree in chemistry, engineering, natural sciences, or related field.
• 10–12 years of pharmaceutical industry experience, including leadership roles.
• Extensive knowledge of Quality Assurance and Quality Control.
• Strong knowledge of cGMP, ICH, and global quality regulations.
• Proven leadership of large, multi-level or multi-shift organizations.
• Ability to manage multiple priorities and deliver results on time.
• Ability to solve problems and work independently with minimal supervision.
• Strong written, verbal, presentation, and organizational skills.
• Demonstrable leadership experience at Catalent may be considered in place of external experience.

Responsibilities

• Lead the site Quality function and Quality Management System to ensure compliance with regulatory, corporate, and customer requirements.
• Develop quality strategy, staffing plans, site quality metrics, and management reviews while fostering a patient-first culture.
• Oversee Quality Assurance and Quality Control and act as the site’s most responsible person for batch disposition.
• Partner with customers and internal teams to resolve quality issues and serve as a member of the Site Leadership Team.
• Maintain regulatory and customer compliance across the site.
• Manage audits, inspections, and remediation activities successfully.
• Establish and track site quality metrics and Quality Unit objectives.
• Develop and execute the site Quality Plan and Quality Unit objectives.
• Maintain and improve the Quality Management System.
• Lead, develop, and manage Quality Assurance and Quality Control teams.
• Serve as primary contact for customers and regulatory agencies.
• Review and approve materials, products, batch records, and quality documentation.
• Manage audits, supplier oversight, training programs, and departmental budget.

Skills

Quality Assurance

Quality Control

cGMP knowledge

ICH knowledge

Leadership

Regulatory audits

Batch disposition

Education

Bachelor's degree in chemistry or related field

Job description

About Site

Our U.S. commercial cell therapy manufacturing facility is located in Princeton, NJ, and is part of Catalent’s cell therapy network including our European Center of Excellence for cell therapy in Gosselies, Belgium.

Position Summary

We have an opportunity for a Director, Quality to join our team. In this role, you will set the strategic direction for quality, ensure proper staffing, and maintain the Quality Management System to meet regulatory, corporate, and customer requirements. You will lead site metrics, management reviews, and foster a Patient First culture. This position oversees Quality Assurance and Quality Control and serves as the most responsible person for batch disposition. You will also provide project guidance and work with customers to resolve quality concerns.

Location

Princeton, NJ
100% Onsite

The Role

• Lead the site Quality function and Quality Management System to ensure compliance with regulatory, corporate, and customer requirements.

• Develop quality strategy, staffing plans, site quality metrics, and management reviews while fostering a patient-first culture.

• Oversee Quality Assurance and Quality Control and act as the site’s most responsible person for batch disposition.

• Partner with customers and internal teams to resolve quality issues and serve as a member of the Site Leadership Team.

• Maintain regulatory and customer compliance across the site.

• Manage audits, inspections, and remediation activities successfully.

• Establish and track site quality metrics and Quality Unit objectives.

• Develop and execute the site Quality Plan and Quality Unit objectives.

• Maintain and improve the Quality Management System.

• Lead, develop, and manage Quality Assurance and Quality Control teams.

• Serve as primary contact for customers and regulatory agencies.

• Review and approve materials, products, batch records, and quality documentation.

• Manage audits, supplier oversight, training programs, and departmental budget.

The Candidate

Minimum Requirements

• Bachelor’s degree in chemistry, engineering, natural sciences, or related field.

• 10–12 years of pharmaceutical industry experience, including leadership roles.

• Extensive knowledge of Quality Assurance and Quality Control.

• Strong knowledge of current Good Manufacturing Practices (cGMP), International Council for Harmonisation (ICH), and global quality regulations.

• Proven leadership of large, multi-level or multi-shift organizations.

• Ability to manage multiple priorities and deliver results on time.

• Ability to solve problems and work independently with minimal supervision.

• Strong written, verbal, presentation, and organizational skills.

• Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent‑sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.

Preferred Skills & Background

• Experience with sterile drug product manufacturing.

• Experience with drug substance manufacturing.

• Experience with Cell Therapy.

• Experience leading manufacturing site operations.

• Ability to work effectively in a start-up environment.

• Comfortable making decisions in ambiguous situations.

• Experience interacting with regulatory agencies and customers.

• Experience managing regulatory and customer audits.

• Experience with quality systems, validation, and supplier oversight.

• Ability to drive quality-related projects through completion.

Pay

The anticipated salary range for this position in NJ is $190,000 – $230,000 Plus Bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.

Why You Should Join Catalent

• Defined career path and annual performance review and feedback process.

• Diverse, inclusive culture.

• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.

• Competitive paid time off plus 8 paid holidays.

• Community engagement and green initiatives.

• Medical, dental, and vision benefits effective day one of employment.

• Tuition Reimbursement.

Catalent offers rewarding opportunities to further your career!

Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

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