Senior Process Engineer

About Site 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. Position Summary We have an opportunity for a Senior Process Engineer to join our team supporting the introduction of new biopharmaceutical products at our development and manufacturing sites. This role focuses on liquid formulations produced under single-use systems in a cleanroom environment. The position involves onboarding new process equipment, coordinating commissioning and qualification, and ensuring validated equipment status. It is a full-time, hands-on engineering role within a growing CDMO, offering the chance to make a meaningful impact in a dynamic environment. Shift: Monday-Friday 8am-5pm Location: Harmans, MD - BWI 100% Onsite The Role Provide hands-on support as a bioprocess equipment subject matter expert and manufacturing support engineer. Support manufacturing floor operations by troubleshooting bioreactors, fermenters, chromatography skids, centrifuges, fillers, isolators, incubators, and utility systems. Collaborate with operators, mechanics, MS&T, and Quality to minimize downtime and resolve equipment issues. Execute preventive maintenance programs and close maintenance work orders within the CMMS system. Coordinate repairs with vendors and maintenance technicians, managing spare parts and reliability improvements. Lead installation of new equipment and support commissioning and qualification activities (IQ/OQ). Contribute to facility expansions and technology transfers, working with Validation and Automation teams on SCADA integration. Prepare and review GMP documentation including change controls, deviations, CAPAs, SOP revisions, and engineering reports. Perform root cause investigations and risk assessments using tools such as FMEA, Fishbone, and 5-Why. Train operators, mechanics, and engineers, and support regulatory inspections as the equipment SME. Manage contractors and vendors and present engineering updates to leadership and project teams. The Candidate Minimum Requirements Bachelor’s degree in Engineering required; Chemical or Mechanical Engineering preferred. Equivalent combination of education, certifications, and relevant experience may be considered. 5–10 years of engineering or maintenance experience in a GMP-regulated biopharmaceutical or biotechnology manufacturing environment. Experience supporting bioprocess equipment, manufacturing operations, and facility systems. Experience with aseptic processing and fill/finish operations. Experience working within cGMP and regulated pharmaceutical environments. Able to navigate site mechanical spaces, including stairs, ladders, and low overhead areas as needed for project support. May require occasional work in tight or awkward spaces, such as behind equipment or within cleanroom utility chases. Ability to visually inspect equipment, read instruments, and review documentation with clarity and accuracy (corrected vision acceptable). Ability to sit at a desk or computer for periods of time to prepare documentation, reports, and data analyses. Must be able to lift and carry up to 40 pounds occasionally. Manual dexterity sufficient to operate tools, instruments, laptops, and measurement equipment. Use of personal protective equipment (PPE) including lab coats, gloves, safety goggles, and, when required, respiratory protection. Preferred Skills & Background Biopharmaceutical manufacturing (strongly preferred). CDMO experience (Catalent, Lonza, Thermo Fisher, Fujifilm Diosynth, AGC Biologics, Resilience, WuXi, etc.). Sterile injectable or aseptic manufacturing environments. Experience in biologics, cell culture, fermentation, and fill/finish operations. Experience in medical device, vaccine, or biotechnology manufacturing. Experience in adjacent regulated industries with strong process equipment background may be considered. Pay The anticipated salary range for this position in MD is $120,000 – $140,000 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. 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. Competitive paid