Technician - Biomanufacturing, Downstream/mRNA

About the role

Perform basic Downstream purification and mRNA production activities, such as in-vitro transcription (IVT) reactions, chromatography, tangential flow filtration (TFF), viral filtration, and column packing and qualification Accurately follows manufacturing Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) and with a focus on "right first time" execution Documents all activities in accordance with Good Documentation Practices (GDPs) in BPRs, Forms, and other quality documentation Recognizes deviations from the intended procedure and raises awareness through the Rapid Response process Proactively identifies safety, quality, and efficiency improvements; Actively participates in the Catalent Way (Continuous Improvement Culture) May lead "Just Do It" (JDI) Continuous Improvement (CI) activities and engage in implementation of CI projects May coach more junior team members on basic execution activities and act as an "onboarding buddy" to facilitate bringing new team members quickly up to speed on culture and basic workplace expectations Performs general cleanroom housekeeping, including room and equipment cleaning, disposal of waste, and maintenance of 5S standards Other duties as assigned The Candidate: Must have High School Diploma or equivalent plus at least two (2) years of relevant experience. We will also accept a Bachelors or Associates Degree in a scientific, engineering, or biomanufacturing discipline without any formal experience GMP manufacturing experience preferred Ability to use Microsoft Word and Excel, and other Office systems GMP manufacturing experience preferred Preferred experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, Chromatography software Physical requirements: This position requires frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities for the position. Working conditions will be Heating Ventilation and Air Conditioned controlled. Ability to operate within a clean room environment as needed. Why you should join Catalent: Defined career path and annual performance review and feedback process Diverse, inclusive culture 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 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 DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due