Senior Scientist Downstream Process Development, mRNA
Job Location:
Madison, OH - USA
Monthly Salary:
Posted on:
Vacancies:
Job Summary
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 andoptimizeIVT reactions enzymatic processing andpurificationworkflows
- Develop scale-down models and execute DOE studies for process characterization andprocess development
- Author process development reports validation protocols and risk assessments (FMEA CPP identification)
- Definea 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 andmaintainSOPs for mRNA synthesisandpurification to ensure reproducibility and compliance
- Collaborate with analytical teams for method development and validation of mRNA 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 modalitiespreferred.
- 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
- Operatingmaintaining and troubleshooting chromatographyworkstationsand 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 staffregardinglaboratory procedures and scientific projects
- Other duties as assigned.
The Candidate:
- Bachelors degree in a STEM discipline and 8-15 years related experience OR
- Masters degree in a STEM discipline and 5-10 years related experience OR
- Doctorate Degree in a STEM discipline and 24 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 7000 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 . 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 for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Required Experience:
Senior IC
About Company
Providing CDMO services, delivery technologies and manufacturing solutions to develop pharmaceuticals, biologics and consumer health products.
