Catalent Pharma Solutions Inc

Scientist - Cell Line Development

Catalent Pharma Solutions Inc$88K — $105K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's in STEM with 6+ years experience, Master's with 3+ years, or PhD with 0-2 years experience.
  • Hands-on mammalian cell culture and aseptic techniques.
  • Independent execution and documentation of complex lab experiments.
  • Strong technical writing and data integrity understanding.
  • Demonstrated problem-solving skills and clear communication of technical findings.
  • Proficiency in Microsoft Office and lab data systems.

Responsibilities

  • Perform bench-scale cell culture work and seed train scale-up.
  • Execute cell pool creation, productivity testing, and clonal selection.
  • Conduct stability testing post-Master Cell Bank creation and coordinate with upstream teams.
  • Analyze data using statistical software and maintain documentation in line with SOPs.
  • Author and review technical documents like study protocols and reports.
  • Act as a technical resource, communicating progress to teams and clients.
  • Support lab operations, equipment maintenance, and organization.

Benefits

  • Key role in a leading global CDMO.
  • Day-one medical, dental, and vision coverage.
  • 401(k) with company match.
  • Tuition reimbursement and professional development opportunities.
  • Generous paid time off and holiday schedule.
  • Collaborative culture focused on improving global patient outcomes.
Full Job Description

Scientist – Cell Line Development

Catalent is seeking a Scientist - Cell Line Development to support the creation, selection, and evaluation of high-producing mammalian cell lines using our proprietary GPEx® suite of technologies and transfection platforms.

This role contributes to projects across multiple development stages, from initial vector insertion through clonal selection and research cell banking for client and internal programs. The successful candidate will combine strong laboratory bench expertise with cell culture techniques, data analysis, and technical client communication to deliver high-quality cell lines for biologic therapies.

Location: 100% Onsite at our facility in Madison, Wisconsin

Shift: Monday – Friday, First Shift

Key Responsibilities:

  • Perform bench-scale cell culture work, including cell bank vial thaws, transfection, seed train scale-up, and cell line expansion within biosafety cabinets.
  • Execute cell pool creation, fed-batch productivity testing, clonal selection, and research cell bank creation stored in liquid nitrogen.
  • Conduct stability testing post-Master Cell Bank (MCB) creation and coordinate hand-offs with Upstream Process Development (US PD) for bioreactor evaluation.
  • Analyze experimental data using statistical software (DoE) and maintain detailed Batch Production Records (BPRs) and laboratory documentation in accordance with SOPs.
  • Author and review technical documents, including study protocols, batch records, test reports, and standard operating procedures.
  • Serve as a technical resource for internal teams and external clients by communicating project progress, utilizing standard templates to present data, and supporting technical project execution.
  • Support essential laboratory operations, equipment maintenance and cleaning, lab stocking, and 5S organization.
  • Other responsibilities as needed.

Required Qualifications:

  • Bachelor's degree in a STEM discipline with a minimum of 6 years relevant experience, Master's degree with a minimum of 3 years relevant experience, or PhD with 0–2 years relevant experience.

  • Hands-on experience with mammalian cell culture, aseptic techniques, biosafety cabinet operations, and routine cell culture maintenance.

  • Ability to independently execute, analyze, and document complex laboratory experiments in a fast-paced environment.

  • Strong technical writing skills and understanding of documentation practices, data integrity requirements, and protocol/report authoring.

  • Demonstrated problem-solving skills with the ability to interpret biological data, identify process improvements, and communicate technical findings clearly.

  • Proficiency with Microsoft Office applications and standard lab data systems.

Preferred Qualifications:

  • Direct experience with transfections, cell bank creation, or cell line development workflows.

  • Experience transitioning from upstream manufacturing or biomanufacturing roles into cell line development.

  • Working knowledge of statistical analysis tools, including Design of Experiments (DOE) and JMP.

  • Familiarity with high-throughput platforms (such as Beacon or Ambr systems) or bench-scale bioreactors.

  • Previous client-facing communication or technical presentation experience.

Why you should join Catalent:

  • Opportunity to play a key role in driving growth within a global CDMO leader.

  • Competitive compensation package, including incentive opportunity.

  • Day-one medical, dental, and vision coverage.

  • 401(k) with company match.

  • Tuition reimbursement and professional development opportunities.

  • Generous paid time off and holiday schedule (152 hours + 8 holidays.)

  • Collaborative, mission-driven culture focused on improving patient outcomes worldwide.

About Catalent Pharma Solutions Inc

Catalent Pharma Solutions Inc is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene therapies, and consumer health products. The company operates in four segments: Softgel and Oral Technologies, Biologics, Oral and Specialty Delivery, and Clinical Supply Services. Catalent Pharma Solutions serves customers in various industries, including pharmaceuticals, biotechnology, and consumer health. The company was founded in 2007 and is headquartered in Somerset, New Jersey.
Learn more about Catalent Pharma Solutions Inc
Size
14,000 employees
Industry
Founded
2007

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