Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities is located 5 miles from the Baltimore Washington International (BWI) airport and 13 miles from our Baltimore location. The campus is close to Washington, DC’s I-270 Technology Corridor, top universities, and government agencies.
The Harmans/BWI-1 EMA and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse.
The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage warehousing.
Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including AAV and other viral vector-based therapies and vaccines.
We have an opportunity for an Engineer I, MS&T to join our team and support GMP manufacturing operations as a project leader for the transfer and startup of clinical drug substance and drug product. You will help translate client and Process Development information into cGMP processes. This role requires hands-on work in a cleanroom and collaboration in a fast-paced, cross-functional environment. The Engineer I, MS&T will report to the Manager, MS&T.
Shift: Monday – Friday, 8am - 5pm
Location: Harmans, MD - BWI
100% Onsite
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Partner with GMP manufacturing and Process Development teams as MS&T project lead and subject matter expert in areas such as cell culture, purification, and fill & finish processes.
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Serve as team leader for process and product investigations and author investigation reports.
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Lead MS&T tech transfer projects from Catalent Process Development and external clients into GMP manufacturing.
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Author tech transfer documents, Master Production Records, and Standard Operating Procedures to support GMP manufacturing projects.
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Work closely with Program Management to ensure MS&T project milestones are achieved, attending meetings as required.
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Collect and trend process data for client and internal review.
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Assist with training GMP Manufacturing staff on client processes.
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Evaluate and recommend equipment and disposable systems for client projects.
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Perform facility fit assessments, process modeling, and Continued Process Verification statistical analysis.
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Other duties as assigned.
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Bachelor of Science in Chemical Engineering, Chemistry, Biology, Life Sciences, or related field with 2+ years of experience in the pharmaceutical or biotechnology industry, or Master of Science in these fields with 1+ years of experience.
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Knowledge and expertise in protein and virus manufacturing in a cGMP environment.
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Experience in one or more manufacturing areas: cell and/or microbial culture, protein purification, and fill/finish.
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On-site presence required, as the role involves time on the manufacturing floor and cross-functional collaboration.
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Experience with process modeling software such as SuperPro, JMP, MatLab, or Aspen is a plus.
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Experience in a Contract Manufacturing Organization environment or similar client-focused work setting is a plus.
The anticipated salary range for this position in MD is $80,000 – $90,000 Plus Bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
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Defined career path and annual performance review and feedback process.
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Diverse, inclusive culture.
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Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
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Competitive paid time off plus 8 paid holidays.
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Community engagement and green initiatives.
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Medical, dental, and vision benefits effective day one of employment.
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Tuition reimbursement.
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.
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