Senior Scientist, QC Analytical

Senior Scientist, QC Analytical 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 Scientist, QC Analytical to join our team. In this role, you will support analytical testing to ensure GMP manufacturing for clinical and commercial clients. You will apply your technical knowledge, regulatory understanding, and commitment to scientific excellence to deliver high-quality results. This position reports to the Sr. Manager, Quality and offers the chance to work in a dynamic, fast-paced environment. Shift: Monday – Friday, 8am-5pm Location: Harmans, MD - BWI 100% Onsite The Role Perform and support a broad range of analytical and molecular biology assays, including ELISA, qPCR, ddPCR, HPLC, capillary electrophoresis, DNA/RNA extraction, and related quality control testing. Troubleshoot laboratory, testing, and instrumentation issues, elevate concerns as needed, and recommend solutions to support batch release, stability, and special testing programs. Serve as a subject matter expert for key analytical techniques, providing technical guidance to auditors, vendors, and cross-functional teams. Mentor, train, and develop laboratory staff while promoting technical excellence and adherence to quality standards. Lead and support continuous improvement initiatives to enhance laboratory efficiency, compliance, and operational performance. Create, revise, and maintain technical documentation, including assay protocols, SOPs, summary reports, and other GMP-controlled records. Review laboratory work, approve data packages, and ensure accurate data interpretation and reporting in accordance with quality requirements. Manage and support change controls (CRs), CAPAs, deviations, OOS investigations, and issue resolution activities to ensure product quality and compliance. Monitor laboratory equipment performance, including maintenance, troubleshooting, alarm response, and coordination of corrective actions. Communicate quality-impacting issues to management and maintain flexibility to support unique production campaigns, including off-hours and weekend operations when required. Other duties as assigned The Candidate Minimum Requirements Bachelor’s degree in a Life Sciences discipline with 4–6 years of experience in a cGMP QC laboratory, or Master’s degree in a Life Sciences discipline with at least 2 years of experience in a cGMP QC laboratory Knowledge and expertise in QC analytical methods used for protein chemistry and molecular biology Experience in the biologic, pharmaceutical, or medical device industry performing hands‑on QC work with strong familiarity of GMP practices Experience in writing Standard Operating Procedures (SOPs) Broad experience with biochemistry and related documentation Proficient in applying basic scientific and regulatory principles to solve operational and quality tasks Experience with Microsoft Excel and Microsoft Word Strong attention to detail and organizational skills Ability to succeed in a team‑oriented environment under dynamic conditions Ability to work a set shift with occasional overtime as required Preferred Skills & Background Experience with techniques such as ELISA, qPCR, ddPCR, HPLC, and Capillary Electrophoresis Pay The anticipated hourly rate for this position in MD is $50.48 – $57.69 Plus Bonus. The final hourly rate 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 time off plus 8 paid holidays Community engagement and green initiatives Medical, dental, and vision benefits effective day one of employment 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. 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 View email address on click.appcast.io. 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. #J-18808-Ljbffr Catalent Pharma Solutions