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Catalent

Global contract drug formulation, manufacturing, packaging

Laboratory Team Leader

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeGreenville, NC, USANo salary listed

About the Job

Requirements

  • An associate degree in Biotechnology, Chemistry, or an equivalent science degree, with nine years of professional experience in pharmaceutical analytical chemistry.
  • A BS or BA degree in a science-related field, such as Biology, Chemistry, or Pharmaceutical Sciences, with eight years of professional experience in pharmaceutical analytical chemistry.
  • A master's degree in a science-related field, with six years of professional experience in pharmaceutical analytical chemistry.
  • A PhD in a science-related field, with four years of relevant experience in pharmaceutical analytical chemistry.
  • At least one year of experience with people leadership and client-facing project management is strongly preferred.
  • Ability to lift 10–50 pounds unassisted.
  • Ability to spend most of the workday standing, walking, lifting, pulling, and pushing.
  • Ability to bend, squat, crawl, climb, and reach.
  • Ability to work with some exposure to hazardous chemicals and other active chemical ingredients.
  • Ability to communicate effectively using speech, vision, and hearing.

Responsibilities

  • Lead laboratory personnel in daily activities, providing coaching and feedback to team members.
  • Provide laboratory support for internal business units and external client pre-commercial and commercial processes and projects.
  • Lead analytical teams in method development, validation, and testing for oral solid dosage forms.
  • Ensure high-quality data generation, regulatory compliance, and efficient project execution across commercial and pre-commercial manufacturing and packaging operations.
  • Supervise, guide, and oversee learning and development needs for a team of approximately three to six scientists and other laboratory personnel at various levels.
  • Manage the development and performance of direct reports, including training, coaching, and mentoring.
  • Lead development of a climate of quality and safety within teams by identifying and monitoring quality and safety standards.
  • Ensure work is performed and documented according to approved standard operating procedures, in general compliance with current Good Manufacturing Practices, and on schedule.
  • Maintain proficiency in process and data review within the respective scientific field of operation and troubleshoot instrument-, method-, and technique-related issues.
  • Manage projects and serve as the analytical representative for internal and external clients, including commercial and pre-commercial clients and, as required, contract manufacturing organizations.
  • Author and review analytical procedures, validation documents, and portions of regulatory submissions for site pre-commercial and commercial projects relating to Analytical.

Desired Qualifications

  • At least one year of experience with people leadership and client-facing project management.

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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