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Catalent

Global contract drug formulation, manufacturing, packaging

Development Scientist 2

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeGreenville, NC, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in Pharmacy, Chemistry, Biology, or a related field and eight or more years of pharmaceutical development experience focused on solids formulation; or a master's degree in Pharmacy, Pharmaceutics, Industry Pharmacy, or a related field and six or more years of pharmaceutical development experience; or a Ph.D. in Pharmacy, Pharmaceutics, Industry Pharmacy, or a related field and four or more years of pharmaceutical development experience.
  • Some exposure to hazardous chemicals and other active chemical ingredients.
  • The capacity to handle and manipulate objects using hands and arms.
  • The ability to occasionally lift items in excess of 50 pounds.
  • The ability to wear a respirator, contingent on completing a medical evaluation with satisfactory results.

Responsibilities

  • Serve as a primary point of contact with clients regarding pharmaceutical development and clinical manufacturing project activities.
  • Support supervision, process development, clinical trial batch manufacturing, packaging, and documentation activities.
  • Manage formulation and process development for several ongoing projects, including project management and customer contact.
  • Maintain GMP compliance in formulation and process development.
  • Assist with planning and operating within a budget for the pharmaceutical area.
  • Work directly with customers and potential customers to agree on development approaches and scope of work.
  • Assist the manufacturing group with batch manufacture and packaging and labeling, including set-up and cleaning.
  • Lead efforts to solve formulation and process problems.
  • Write batch records, SOPs, IQ/OQ/PQ documents, development and technical reports, and CMC sections for regulatory submissions as directed.
  • Ensure work is accurate, precise, properly documented, and performed within GMP guidelines when appropriate.

About the Company

Catalent

Global contract drug formulation, manufacturing, packaging

Catalent provides end-to-end contract development and manufacturing services for pharmaceutical, biotechnology, and consumer health products. Its offerings cover drug formulation, large-scale manufacturing, clinical supply, and packaging under long-term partnerships, coordinating through a connected supply chain to move products from development to market. It differentiates itself with a broad, integrated service platform and long-standing customer relationships that help clients accelerate development and ensure reliable supply. The company aims to help clients bring products to market efficiently while balancing quality, cost, and sustainability across the product lifecycle.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Franklin Township, NJ
Founded
1996

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