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Catalent

Global contract drug formulation, manufacturing, packaging

Manager – Molecular & Cellular Biology

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

About the Job

Requirements

  • A bachelor's degree in a relevant scientific discipline and at least 5 years of experience with department-specific analytical, molecular, and cellular biology techniques.
  • At least 2 years of people management or laboratory leadership experience, including team supervision, performance management, and staff development.
  • Knowledge of principles, theories, and concepts applicable to a wide range of work in a discipline such as Biology, Chemistry, or Biochemistry, and broad knowledge of principles and concepts in other disciplines.
  • In-depth knowledge of instrumentation, theory, data interpretation, and applications in at least one technical area, with the ability to assess new technologies and their impact on Catalent offerings.
  • Experience in most aspects of drug development and lifecycle support, and the ability to develop strategies and tactics to meet regulatory milestones.
  • Ability to communicate complex technical information to non-technical audiences.
  • Ability to lead difficult discussions with customers and drive them to an acceptable resolution.
  • Physical ability to frequently stand, sit, reach, and walk; occasionally lift up to 40 pounds, push up to 35 pounds, and pull up to 35 pounds; and rarely kneel. The work environment includes occasional exposure to extreme cold, noise, and vibration; frequent exposure to hazards; and rare exposure to extreme heat, humidity, wet conditions, and temperature changes.
  • Demonstrable leadership experience at Catalent, including participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW, may be considered in place of external experience.

Responsibilities

  • Serve as a technical expert supporting Large Molecule/Biologics programs, including mammalian cell culture, sterile technique, cell-based assays, ELISA-based potency and quantitative assays, and molecular biology techniques such as quantitative polymerase chain reaction and polymerase chain reaction.
  • Provide expertise in advanced analytical technologies, including flow cytometry, kinetic binding assessment using biolayer interferometry or surface plasmon resonance, and other scientific platforms required to support client and business objectives.
  • Lead and oversee method development, feasibility assessments, transfers, verifications, qualifications, validations, stability studies, and ad hoc testing within the Molecular and Cellular Biology laboratory.
  • Plan, prioritize, and manage analytical workflows to ensure projects are executed in accordance with client contracts, technical agreements, quality standards, and business goals.
  • Serve as a Technical Lead or backup Technical Lead, providing scientific leadership, technical direction, and project oversight for Molecular and Cellular Biology programs.
  • Ensure laboratory compliance by managing computer system validation activities, maintaining qualified instrument and equipment status, and enforcing current Good Manufacturing Practice requirements.
  • Drive data integrity and quality by reviewing analytical results, verifying peer data, and ensuring adherence to standard operating procedures, client requirements, Good Manufacturing Practice standards, and safety regulations.
  • Manage project timelines, budgets, resource allocation, and revenue forecasting while supporting proposal development, project costing, and business growth initiatives.
  • Lead, develop, and mentor laboratory personnel through performance management, training coordination, employee engagement, succession planning, and fostering a culture of continuous learning.
  • Promote a culture of quality, safety, ethics, and innovation by supporting cross-functional collaboration, implementing new technologies, supporting business development activities, and enhancing biopharmaceutical service offerings.
  • Perform other duties as assigned.

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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