Catalent

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Catalent Inc. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Pharmaceutical Manufacturing Operator Position Summary Work Schedule: Monday – Thursday, 1:30PM – 12:00AM 100% onsite Start your career where science meets purpose. At Catalent , we don’t just make medicine—we help people live better, longer lives. As a Pharmaceutical Manufacturing Operator , you’ll be part of a team that transforms scientific breakthroughs into life-saving treatments. This is more than a job. It’s a career launchpad in a growing industry...

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. The Boston-area facility is Catalent’s global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The...

General Manager-Inhalation Site- Chelsea, MA Position Summary Reporting to the VP Operations, Respiratory, Ophthalmic & Analytical the General Manager has overall responsibility for the safe and efficient operation of the Chelsea, MA (Greater Boston) site. The Chelsea, MA facility is Catalent’s global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. The Role Manage safety, quality, service, and cost associated with an entire production facility and ensure compliance with Health, Safety and Environmental policies and regulations. Drive improvements within the site to achieve performance objectives Build talent and capabilities across the site to ensure the current and future health of the site Direct the development, growth and ongoing profitability of the site....

Position Summary: Work Schedule: Monday – Friday, 6:30AM – 3:00PM 100% onsite Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions—from science and engineering to operations and logistics. The Pharmaceutical Packaging Technician II is responsible for running various types of production equipment in primary and/or secondary packaging. The Role: Inspect drug products, components, and labels for accuracy and quality Follow safety, quality, and compliance standards during packaging operations Execute batch records for clinical and commercial packaging Report any issues or deviations promptly Maintain accurate documentation in line with SOPs and cGMP All other duties as assigned...

Position Summary Spring/Summer Internship 2026 This position is 100% on-site in Winchester, Kentucky. Catalent’s Winchester location is the flagship US manufacturing location for large scale oral dose forms, with integrated analytical and development services. With 28 years of expertise in product development, technology transfers and commercial manufacturing, and roots in industry-leading Glatt technology. The Product Development (PD) Intern is responsible for supporting the product development team, both during the execution of development projects, writing development protocols and reports, performing physical testing and assisting in manufacturing execution. The Product Development Intern communicates and interacts with product development and other department team members to ensure assigned tasks are completed in a timely manner. The Role Gather and summarize data from executed batch record Collecting PD-related physical testing data from manufactured...

Position Summary: Work Schedule: Monday – Friday, 8AM – 4:30PM 100% onsite (Kansas City) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our large molecule analytical team has over 25 years of experience providing broad-based and orthogonal analytical CMC services for stand-alone and integrated biologics projects. We provide support for drug substance, drug product, and intermediates for both innovator and biosimilar/biobetter products. Catalent Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II in Commercial Testing who will primarily be responsible for testing samples and reporting data under Good Manufacturing Practice (cGMP) regulatory guidance for Large Molecules/Biologics product development, release and related stability studies. The Role: Execute laboratory testing using the following...

Position Summary Shift: Monday-Friday 8am-5pm 100% on-site 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’s Kansas City facility is home to our Oral & Specialty Drug Delivery,...

Position Summary: Work Schedule: Monday – Friday, core hours 8am-5pm 100% on-site (Madison, WI) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics. The Materials Management department is responsible for warehouse management, inventory control, work order management, incoming receipts, and domestic and international shipments of all items for Madison. This department follows approved materials SOPs for the Madison site. The Materials Management Team supports other departments in all materials needs, including staging materials for manufacturing. The Specialist I - Materials...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Catalent Inc. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Associate Scientist II - Biochemical Analysis Position Summary Work Schedule: Monday - Friday, 8AM - 4:30PM 100% onsite (Kansas City) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our large molecule analytical team has over 25 years of experience providing broad-based and orthogonal analytical CMC services for...

Associate Director, Quality Assurance Position Summary: 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. This is a full-time salaried position, onsite out of Philadelphia, PA. The Associate...