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Catalent, Inc.

Quality Control Analyst II - Analytical

12 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

Quality Control Analyst responsible for executing QC testing and analytical activities supporting product development, release, and stability. Conducts chemical and physical analyses, compiles data, participates in investigations, and reviews data for compliance. Operates analytical instrumentation, monitors equipment, and assists in SOP construction and updating. Bachelor's degree in Physical or Chemical Sciences with 2+ years of experience in a GMP environment required.

Catalent, Inc.

Process Engineer

12 Hours Ago

Chelsea, MA, USA

13,715 Employees

1-3 Years of Experience

Apply

13,715 Employees

1-3 Years of Experience

Biotech • Pharmaceutical

The Process Engineer at Catalent Pharma Solutions in Chelsea, MA is responsible for assisting in the design and implementation of manufacturing processes, instrumentation, and equipment for clinical and commercial manufacturing. They also participate in technology transfer, process optimization, and process validation activities.

Catalent, Inc.

Senior Scientist, QC

12 Hours Ago

Bloomington, MN, USA

13,715 Employees

5-7 Years of Experience

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13,715 Employees

5-7 Years of Experience

Biotech • Pharmaceutical

The Senior Scientist, QC is responsible for executing and documenting cGMP Quality Control testing, operating quality control equipment, assisting with technical document preparation, and performing lab housekeeping, while ensuring compliance with GMP standards and conducting microbial control evaluations.

Catalent, Inc.

Scientist, QC Analytical

12 Hours Ago

Harmans, MD, USA

13,715 Employees

1-3 Years of Experience

Apply

13,715 Employees

1-3 Years of Experience

Biotech • Pharmaceutical

The Scientist, QC Analytical at Catalent is responsible for supporting analytical testing in GMP manufacturing for clinical and commercial clients. They perform various assays, document testing procedures, generate internal and external documents, provide analytical support, and ensure instrumentation care and maintenance. The role requires a Master's in Life Sciences and 0-2 years of experience in a cGMP QC laboratory.

Catalent, Inc.

Supervisor, QC Analytical

12 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

Supervisor, QC Analytical responsible for leading analytical testing, investigations, and key deliverables for the Quality Control (QC) group. Must demonstrate expert technical knowledge, mentor direct reports, drive compliance, and maintain a strong cGMP understanding. Oversees assays such as ELISA, DNA/RNA extraction, gel electrophoresis, qPCR, RT-PCR, HPLC, and Capillary Electrophoresis. Builds effective teams, drives engagement, and ensures quality results.

Catalent, Inc.

Cost Accountant

12 Hours Ago

Philadelphia, PA, USA

13,715 Employees

1-3 Years of Experience

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13,715 Employees

1-3 Years of Experience

Biotech • Pharmaceutical

The Cost Accountant at Catalent is responsible for analyzing inventory, standard costing, and manufacturing performance. Duties include monthly closing assistance, financial reporting, account reconciliations, and supporting the Oral & Specialty Delivery business unit with reporting and analysis.

Catalent, Inc.

Account Executive, Wellness

12 Hours Ago

Field, KY, USA

13,715 Employees

3-5 Years of Experience

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13,715 Employees

3-5 Years of Experience

Biotech • Pharmaceutical

The Account Executive, Wellness is responsible for growing Catalent’s Consumer Healthcare business in the US and Canada by managing customer relationships, developing account plans, and driving new business through sales funnel development. This is a field-based, remote role with travel required. The role involves internal coordination, opportunity management, customer interaction, and market analysis.

Catalent, Inc.

Engineer III, MS&T

12 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 Manufacturing Sciences & Technology (MS&T) Engineer III at Catalent Gene Therapy supports the technical transfer and startup of clinical drug manufacturing operations. Responsibilities include serving as a subject matter expert for biologic processes, authoring tech transfer documents, training manufacturing staff, and leading investigations. Requires 4-8 years experience with expertise in protein and virus manufacturing in a cGMP environment.

Catalent, Inc.

Senior Process Engineer

12 Hours Ago

Bloomington, MN, USA

13,715 Employees

5-7 Years of Experience

Apply

13,715 Employees

5-7 Years of Experience

Biotech • Pharmaceutical

The Senior Process Engineer will oversee and optimize manufacturing processes for sterile biologic drug products, assisting in troubleshooting and identifying improvements. The role involves managing project budgets and schedules and serving as a Subject Matter Expert on validated systems to enhance product quality and efficiency.

Catalent, Inc.

Process Engineer, MS&T

12 Hours Ago

Princeton, NJ, USA

13,715 Employees

5-7 Years of Experience

Apply

13,715 Employees

5-7 Years of Experience

Biotech • Pharmaceutical

The Process Engineer at Catalent Pharma Solutions in Princeton, NJ provides technical support to manufacturing processes in a GMP environment, troubleshoots process and equipment issues, and drives continuous improvements to the manufacturing process. Responsibilities include leading process improvement projects, participating in tech transfers, and ensuring quality compliance.