Hiring.Camp

Manager, Molecular & Cellular Biology

Catalent

·

Yesterday

Location
USA-Kansas City, United States of America
Workplace
Onsite
Type
Full-time
Seniority
Manager
Experience
5+ years
Closing date
Today
Source
Workday

Description

Manager, Molecular & Cellular Biology



About Site

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.



Position Summary

We have an opportunity for a Manager, Molecular & Cellular Biology to join our team. In this role, you will lead sub-teams of scientists and group leaders, serving as a technical expert and ensuring compliance with cGMP standards. You will manage analytical activities for Biopharma product development, support client interactions, and oversee HR responsibilities. This position offers the chance to work on advanced technologies and contribute to the success of large molecule and biologics programs.



Shift: Monday – Friday 8am – 4:30pm
Location: Kansas City, MO
100% Onsite



The role:

  • 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 qPCR and PCR.
  • Provide expertise in advanced analytical technologies, including flow cytometry, kinetic binding assessment (BLI/SPR), 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 cGMP requirements.
  • Drive data integrity and quality by reviewing analytical results, verifying peer data, and ensuring adherence to SOPs, client requirements, GMP 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.
  • Champion a culture of quality, safety, ethics, and innovation by promoting cross-functional collaboration, implementing new technologies, supporting business development activities, and enhancing biopharmaceutical service offerings.
  • Other duties as assigned


The candidate:

  • Bachelor’s degree in a relevant scientific discipline with a minimum of 5 years of experience in department-specific analytical, molecular, and cellular biology techniques.
  • Minimum of 2 years of people management or laboratory leadership experience, including team supervision, performance management, and staff development.
  • Applies knowledge of the principles, theories, and concepts applicable to a wide range of work in a discipline (e.g., Biology, Chemistry, Biochemistry) and broad knowledge of principles and concepts in other disciplines.
  • In-depth knowledge in instrumentation, theory, data interpretation and applications in at least one technical area. Can assess new technologies and their impact on Catalent offerings
  • Experienced in most aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones
  • Excellent written and verbal communications skills with internal and external customers, colleagues, and supervisor.
  • Ability to communicate complex technical information to non-technical audiences
  • Able to lead difficult discussions with customers and drive the to an acceptable resolution
  • Physical requirements include frequent standing, sitting, and reaching; constant walking; occasional lifting up to 40 lbs., pushing up to 35 lbs., and pulling up to 35 lbs.; and rare kneeling. Work is performed in an environment with 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 but not limited to participation in Catalent‑sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.


Why you should join Catalent:

  • Competitive medical benefits and 401K
  • 152 hours PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes

Catalent offers rewarding opportunities to further your career!  Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. 


personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.


Catalent is an Equal Opportunity Employer, including disability and veterans.


If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [email protected]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

    

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.


Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [email protected] for us to investigate with local authorities.


California Job Seekers can find our California Job Applicant Notice HERE.


Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.

 

Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.

Skills

Clinical TrialsGMPCompliance

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