Director of Quality

Director Of Quality Malvern Pa

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

Catalent Micron Technologies Malvern facility specializes in particle size reduction technologies and integrated analytical services for the pharmaceutical industry. It is equipped with advanced systems to handle highly potent and cytotoxic compounds, and provide leading analytical services associated with particle size engineering and material characterization testing from early-stage development to commercialization.

As a member of the senior management team, ensure an effective pharmaceutical quality management system is in place. The quality director will provide leadership and daily management of the site quality assurance and analytical laboratory departments. The quality director will also be responsible for providing support to both the malvern site business unit (BU) operations, as well as to the corporate quality function.

Catalent is committed to a patient first culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.

The Role :

• To ensure the quality function complies with health, safety and environmental requirements and employees adhere to the "standards of business conduct."
• To determine, establish and maintain comprehensive systems that establish documents and monitor gmp quality and ISO standards and that meet Catalent, regulatory and customer requirements.
• To ensure that the Malvern site complies with all applicable laws relative to good manufacturing practice and ensure that all regulatory licenses are maintained and renew in line with different countries' requirements as appropriate for the business.
• Manage the team against the site and quality strategy objectives.
• To develop a quality culture on site, such that the quality team provides leadership and coaching to ensure gmp best practices are embedded throughout the site.
• To continually review the operation of the quality function on site, and deliver a program of continual improvement.
• To manage the quality budget, ensuring well defined resource modelling.
• To act as a primary contact for senior quality professionals within our customer organizations to ensure compliance and customer service standards are met.
• Other duties as assigned.

The Candidate :

Why You Should Join Catalent :

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.