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Catalent, Inc.

CI Manager

13 Hours Ago

Greendale, IN, USA

13,715 Employees

5-7 Years of Experience

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13,715 Employees

5-7 Years of Experience

Biotech • Pharmaceutical

The CI Manager at Catalent in Greendale, Indiana is responsible for driving continuous improvement and operational excellence through lean manufacturing methodologies and leading CI initiatives in a manufacturing environment. Key responsibilities include driving productivity gains, implementing Lean manufacturing concepts, analyzing data for action plans, developing metrics, and leading Kaizen events. The ideal candidate has a BS/BA in a technical or business major, 5+ years of CI leadership experience, and strong analytical and communication skills.

Catalent, Inc.

Product Development Engineer II

13 Hours Ago

Chelsea, MA, USA

13,715 Employees

1-3 Years of Experience

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13,715 Employees

1-3 Years of Experience

Biotech • Pharmaceutical

The Product Development Engineer II at Catalent will be responsible for supporting product and process development, conducting experiments on pharmaceutical manufacturing equipment, leading technology transfers, performing data analysis, and providing training for manufacturing operations. They will ensure adherence to safety and quality standards throughout the development process.

Catalent, Inc.

Manager, QA Analytical

13 Hours Ago

Harmans, MD, USA

13,715 Employees

7+ Years of Experience

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13,715 Employees

7+ Years of Experience

Biotech • Pharmaceutical

The Manager, QA Analytical oversees QA operations in QC Analytical. Responsibilities include staff training on cGMP procedures, quality review of documentation and analytical methods, interfacing with clients and teams, managing investigations and deviations, and supporting audits and compliance measures in pharmaceutical manufacturing.

Catalent, Inc.

Human Resources Generalist (HRBP)

13 Hours Ago

Harmans, MD, USA

13,715 Employees

5-7 Years of Experience

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13,715 Employees

5-7 Years of Experience

Biotech • Pharmaceutical

The Human Resources Generalist provides HR support in areas such as employee relations, recruitment, performance management, and compliance. They develop training programs, manage employee documentation, and assist with benefits administration and employee engagement initiatives, while also ensuring adherence to company policies and legal regulations.

Catalent, Inc.

Supervisor, QA OTF Support

13 Hours Ago

Harmans, MD, USA

13,715 Employees

5-7 Years of Experience

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13,715 Employees

5-7 Years of Experience

Biotech • Pharmaceutical

The Supervisor, QA OTF Support is responsible for overseeing the QA on the Floor program in a cGMP manufacturing facility. Responsibilities include training staff on cGMP operations, ensuring compliance with manufacturing procedures, providing leadership in quality processes, and driving improvements in quality initiatives. The role requires active presence on the shop floor and collaboration with manufacturing teams to resolve quality issues and enhance operational efficiency.

Catalent, Inc.

Senior Scientist, Analytical Research & Development

13 Hours Ago

St. Petersburg, FL, USA

13,715 Employees

7+ Years of Experience

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13,715 Employees

7+ Years of Experience

Biotech • Pharmaceutical

The Senior Scientist in Analytical Research & Development will develop and validate test methods for drug substances and products, lead analytical method transfer activities, analyze various materials, and ensure compliance with regulatory standards. Responsibilities also include training personnel and conducting laboratory investigations.

Catalent, Inc.

Senior Specialist, QA Analytical

13 Hours Ago

Harmans, MD, USA

13,715 Employees

5-7 Years of Experience

Apply

13,715 Employees

5-7 Years of Experience

Biotech • Pharmaceutical

The Senior Specialist, QA Analytical ensures compliance and quality oversight in the development and manufacturing of biopharmaceuticals. Responsibilities include maintaining quality systems, performing document reviews, supporting client audits, and continuous improvement initiatives.

Catalent, Inc.

Automation Engineer III

13 Hours Ago

Chelsea, MA, USA

13,715 Employees

3-5 Years of Experience

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13,715 Employees

3-5 Years of Experience

Biotech • Pharmaceutical

The Automation Engineer III leads the design and implementation of automation systems for pharmaceutical manufacturing, ensuring compliance with GMP standards. Responsibilities include providing engineering expertise, documenting modifications, troubleshooting control systems, and training users on system functionality. This role involves technical support during the lifecycle of automation systems.

Catalent, Inc.

Development Scientist II

13 Hours Ago

Greenville, NC, USA

13,715 Employees

3-5 Years of Experience

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13,715 Employees

3-5 Years of Experience

Biotech • Pharmaceutical

The Development Scientist II is responsible for pharmaceutical development and clinical manufacturing project activities, including formulation and process development, GMP compliance, budget planning, customer interaction, and documentation writing. The role involves assisting with batch manufacturing and problem-solving in formulation processes while ensuring accuracy and compliance with guidelines.

Catalent, Inc.

Principal Engineer, Continuous Improvement

13 Hours Ago

Harmans, MD, USA

13,715 Employees

7+ Years of Experience

Apply

13,715 Employees

7+ Years of Experience

Biotech • Pharmaceutical

The Principal Continuous Improvement Engineer will lead CI initiatives at a manufacturing facility for gene therapies. Responsibilities include identifying improvement opportunities, facilitating problem-solving, coaching project leaders, and promoting a Continuous Improvement culture. This is a full-time on-site position at the Harmans/BWI campus, focusing on quality, compliance, and patient safety.