Manager, Quality Control
Catalent Pharma SolutionsNew Jersey, United States
Posted May 11, 2026
130000 - 160000 USD
Full Time
About the Company
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. For more information, visit www.catalent.com. Catalyst + Talent. Our name combines these ideas. From drug and biologic development services to delivery technologies to supply solutions, we are the catalyst for your success. We have the deepest expertise, the broadest offerings, and the most innovative technologies to help you get more molecules to market faster, enhance product performance, and provide superior, reliable manufacturing and packaging results. more products. better treatments. reliably supplied.⢠Your talents, ideas, and passion are essential to our mission: to develop, manufacture, and supply products that help people live better, healthier lives. Join us! Catalent hires people with a passion to make a difference to the health of millions of people globally. Your expertise, coupled with Catalentâs advanced technologies and collaboration with thousands of innovative pharmaceutical, biotech, and healthcare companies, will help bring life-enhancing products to life. Grow with us. Be challenged. Make a personal impact.
Job Description
The Manager, Quality Control is responsible for organizing and supervising daily Quality Control activities to ensure testing schedules are executed as planned.
Requirements
- Coordinate the QC lab activities to meet production goals, quality and cost objectives.
- Provide support to analyst in troubleshooting QC testing methods and instruments.
- Supervise daily QC activities and ensure schedule is followed.
- Perform analytical, microbiological and raw material dossier review.
- Review all QC forms and logbooks used for daily operations.
- Assist in OOS investigations.
- Assist in instrument qualifications.
- Lead training of QC analyst.
- Execute Method Validation, IPC, CFP, Microbiological and Raw Material Test.
- Author and revise QC lab documents such as SOP, Specifications, Protocols and Reports.
- Set and ensure a regular follow up of the individual SMART objectives in collaboration with the members of his/her team.
- Implement/ Execute the company strategy and organizes the activities within his/her team.
- Measure the performance of his/her team.
- Share relevant information and communicates with his/her team.
- Develop each team member's autonomy and expertise, through training and any other development opportunity mainly.
- Other duties are assigned.
Benefits
- 152 hours of paid time off annually + 8 paid holidays.
- Medical, dental, vision and 401K benefits effective day one of employment.
- Tuition Reimbursement.
