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Senior Scientist - Downstream Process Development, mRNA

Catalent -
Madison, WI

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Job Details

Full-time

Benefits

Paid holidays
Health insurance
Dental insurance
Tuition reimbursement
Paid time off
Vision insurance
401(k) matching
Benefits from day one

Qualifications

Biochemical laboratory techniques
Chemical separation processes
Laboratory sample purification
Bioprocessing

Full Job Description

Senior Scientist - Downstream Process Development, mRNA

Position Summary:

Work Schedule: M-F 8am-5pm
100% on-site

Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients. Leveraging our growing differentiated technology portfolio, world class manufacturing capability, and other integrated services across the Catalent network, Catalent Biologics is positioned to drive significant growth for Catalent.

Catalent Pharma Solutions in Madison, WI is hiring a Senior Scientist - Downstream Process Development, mRNA. The Process Development Senior Scientist, mRNA will lead and support the development, optimization, and process characterization of manufacturing processes for mRNA-based therapeutics and vaccines, spanning early-phase clinical through commercial programs. This role requires hands-on expertise in mRNA process development, including in vitro transcription (IVT), purification, and analytical characterization. The scientist will bring deep mRNA technical expertise and demonstrate continuous learning and adaptability, recognizing that supporting multiple modalities, including protein biologics, may be required to meet evolving client and business needs.

The Role:

Design and optimize IVT reactions, enzymatic processing, and purification workflows
Develop scale-down models and execute DOE studies for process characterization and process development
Author process development reports, validation protocols, and risk assessments (FMEA, CPP identification)
Define a control strategy for mRNA DS (CPPs, CQAs, IPCs, acceptance criteria, sampling plans) and defending it through late phase / commercial readiness
Apply Quality by Design (QbD) principles and statistical tools for process characterization and PPQ readiness
Ensure compliance with FDA, EMA, and ICH guidelines for process validation and lifecycle management
Establish and maintain SOPs for mRNA synthesis and purification to ensure reproducibility and compliance
Collaborate with analytical teams for method development and validation of mRNA drug substance. Experience authoring or reviewing method validation/qualification strategy and understanding suitability for intended use (development vs GMP release) preferred
Ability to support downstream process development for monoclonal antibodies and other protein modalities preferred.
Participate in tech transfer activities to GMP manufacturing sites for both mRNA and protein programs.
Process scale chromatography and filtration (chromatography, tangential flow, normal flow) experience
Operating, maintaining, and troubleshooting chromatography workstations and process skids preferably in an industrial setting
Process scale up and technology transfer
Knowledge and experience working in a cGMP environment
Good documentation practices (GDP)
Aseptic technique experience
Experience writing standard operating procedures, batch records, and reports
Experience mentoring junior staff regarding laboratory procedures and scientific projects
Other duties as assigned.

The Candidate:

Bachelor's degree in a STEM discipline and 8-15 years related experience, OR
Master's degree in a STEM discipline and 5-10 years related experience, OR
Doctorate Degree in a STEM discipline and 2–4 years related experience
Process scale chromatography and filtration (viral, chromatography, tangential flow,
normal flow) experience
Operating, maintaining, and troubleshooting chromatography workstations and process
skids preferably in an industrial setting
Viral clearance validation, process scale up, and technology transfer
Knowledge and experience working in a cGMP environment
Good documentation practices (GDP)
Aseptic technique experience
Experience writing standard operating procedures, batch records, and reports
Experience mentoring junior staff regarding laboratory procedures and scientific project

Why you should join Catalent:

Defined career path and annual performance review and feedback process
Diverse, inclusive culture
Positive working environment focusing on continually improving processes to remain innovative
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
152 hours of PTO + 8 paid holidays
Generous 401K match
Medical, dental and vision benefits effective day one of employment
Tuition Reimbursement - Let us help you finish your degree or start a new degree!

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.

Apply Now

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