Key Responsibilities
Laboratory Execution: Independently perform downstream purification experiments, including automated chromatography (ÄKTA platforms), filtration, clarification, column packing, and tangential flow filtration (TFF/UF/DF).
Process Development & Optimization: Lead the design, optimization, and characterization of downstream purification operations (including chromatography, depth filtration, and UF/DF) for monoclonal antibodies (mAbs) and bispecific constructs across the full product lifecycle.
Technical Leadership & Client Interaction: Serve as technical lead for client development or transfer projects, effectively communicating project status, technical rationales, and experimental results internally and externally.
Documentation & GMP Compliance: Author, review, and maintain GMP-compliant technical documents—including protocols, SOPs, test reports, and batch production records (BPRs)—in accordance with Good Documentation Practices (GDP).
Data Analysis & Mentorship: Critically analyze complex experimental data using sound scientific judgment, while helping train, coach, and mentor junior team members on laboratory procedures.
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 relevant academic experience.
Hands-on experience with process-scale chromatography and filtration (chromatography, tangential flow filtration, normal flow filtration).
Experience operating, maintaining, and troubleshooting chromatography workstations and process skids (e.g., ÄKTA platforms).
Demonstrated knowledge of protein purification principles, methods, scale-up concepts, and modes of chromatography.
Strong working knowledge of Good Documentation Practices (GDP), aseptic techniques, and technical document authoring (protocols, SOPs, batch records, reports).
Ability to independently design, execute, analyze, and troubleshoot complex laboratory experiments under accelerated timelines.
Proficiency with Microsoft Office applications (Excel, Word) and laboratory or manufacturing software systems.
Preferred Qualifications
Experience in early-stage biologics process development, clone/candidate screening, method adaptation, or process optimization.
Direct experience with technology transfer into cGMP manufacturing, scale-up parameters, viral clearance validation, or process characterization.
Experience in a cGMP-regulated biopharmaceutical, biotechnology, or CDMO environment.
Experience using quality systems for tracking deviations, investigations, and change controls.
Demonstrated experience mentoring and training junior scientific staff.
Excellent client-facing and communication skills, with experience leading technical project discussions and client updates.
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
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.
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