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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 9 years of professional experience in pharmaceutical analytical chemistry.
  • A bachelor's degree in a science-related field, such as Biology, Chemistry, or Pharmaceutical Sciences, with 8 years of professional experience in pharmaceutical analytical chemistry.
  • A master's degree in a science-related field with 6 years of professional experience in pharmaceutical analytical chemistry.
  • A PhD in a science-related field with 4 years of relevant experience in pharmaceutical analytical chemistry.
  • Experience in a Catalent analytical laboratory independently managing client interactions and projects, and mentoring and training junior analysts, may substitute for 3 years of professional experience.
  • Ability to lift up to 10 pounds unassisted.
  • Ability to perform most of the workday while sitting.
  • Ability to work with some exposure to hazardous chemicals and other active chemical ingredients.

Responsibilities

  • Supervise and support the development and growth of chemists and scientists in good manufacturing practice documentation, understanding client project scope, and laboratory technical skills through on-the-job training, mentoring, and guidance.
  • Resolve conflicts within the group relating to performance or workload and ensure proper resource allocation within and across teams.
  • Schedule analytical work and review analytical data packets and analysis reports, as appropriate.
  • Develop and manage the performance of direct reports, including training, coaching, and mentoring.
  • Lead the development of a quality and safety climate within teams by identifying and monitoring quality and safety standards.
  • Ensure work is performed and documented according to approved standard operating procedures, generally in compliance with current good manufacturing practices and within agreed schedules.
  • Maintain proficiency in process and data review within the respective scientific field of operation, troubleshoot instrument-, method-, and technique-related issues as appropriate to job responsibilities.
  • Initiate and perform investigations for out-of-specification and out-of-trend results and deviations from standard operating procedures; ensure timely, comprehensive investigations in compliance with internal procedures and root cause analysis techniques.
  • Identify and recommend opportunities to improve efficiency, customer service, and teamwork within the analytical group, and monitor key performance indicators.
  • 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.

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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