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The Quality Assurance Associate will provide quality support to a Clinical Storage and Distribution facility in Singapore in line with PIC/S Good Manufacturing Practice and Good Distribution Practice. Responsibilities include material review and release, support on Quality matters, CAPA evaluation, Change Control review, validation document approval, batch record review, audit coordination, and more.

The Project Manager at Catalent Pharma Solutions is responsible for leading and managing activities for assigned projects, ensuring timely communication with customers, tracking project progress, and resolving any issues that may arise. The candidate must have exceptional customer service skills, a scientific or engineering background, and experience in the Pharma or Manufacturing industry. Proficiency in MS Project, organizational skills, and the ability to work under pressure are also required.

Catalent is recruiting for a Scientist 2 to conduct analysis for QC Release, Stability, and in-process Validation. Responsibilities include performing Finished Product QC release testing, generating test plans, writing stability reports, interpreting planning tools, identifying laboratory deviations, maintaining laboratory areas, and ensuring compliance with GMP and EH&S.

The Enterprise Data Integrations Specialist at Catalent is responsible for overseeing data integrations between internal and external systems, ensuring optimal performance and value for the company and its customers. Key responsibilities include data discovery, sourcing strategy, maintaining integration standards, and onboarding new data sources. The role requires experience in cloud-to-cloud and on-prem-to-cloud data integration projects, knowledge of Azure Data Factory and Informatica IICS, and expertise in data integration practices and tools.

Operator III, Formulation responsible for measuring and formulating drug products, performing sterile filtration, and cleaning equipment. Full-time role with rotating shifts. Candidates require high school/GED, 3 years of pharmaceutical manufacturing experience, and GMP experience.

The Scientist I - Quality Control position at Catalent Biologics involves routine testing of in-process samples, raw materials, finished goods, and stability samples. Responsibilities include analyzing and interpreting results, data entry/review, equipment maintenance, and adherence to cGMP standards. The candidate must have a degree in Biology, Biotechnology, or Chemistry with varying levels of industry experience or education. Strong emphasis on maintaining Quality Control equipment and knowledge of ELISA, HPLC, and Empower Software.