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 a Senior Specialist QA OTF Support to join our team. This role provides Quality Assurance support for GMP manufacturing of master and working cell banks, biological bulk drug substance, and finished drug product for human use. You will ensure compliance by observing manufacturing operations and reviewing documentation on the floor. The position focuses on maintaining quality standards, supporting continuous improvement, and ensuring adherence to regulatory requirements for biological products.
Shift: Monday – Friday, 8am-5pm
Location: Harmans, MD - BWI
100% Onsite
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Provide dedicated QA quality floor oversight of GMP operations for manufacturing of cell banks, bulk drug substance, and final drug product, spending 75% of the day on the floor
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Perform QA on-the-floor activities including room release, observing critical processes, reviewing batch documentation in real time, and resolving issues during manufacturing
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Partner with Manufacturing and other support teams
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Perform Acceptable Quality Limit (AQL) visual inspection of drug product
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Review and approve batch documents for media and buffer preparation solutions
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Generate or revise GMP documentation such as Standard Operating Procedures, Master Batch Record review, and SMPs
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Compile deviations observed on the floor and ensure timely completion
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Perform audits of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and Good Documentation Practices
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Make quality decisions with limited oversight
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Identify and implement continuous improvement initiatives
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Participate in site and corporate quality and process improvement initiatives
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Guide personnel involved in GMP operations on compliance, internal procedures, regulatory requirements, and industry best practices
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Actively participate in training activities and manage individual training plan
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Other duties as assigned
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Master’s degree in a Scientific, Engineering, or Biotech field with 2–4 years of experience in Quality Assurance, Quality Control, or Manufacturing within biologics, biopharmaceuticals, or a regulated industry, OR
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Bachelor’s degree in a Scientific, Engineering, or Biotech field with 4–6 years of experience in Quality Assurance, Quality Control, or Manufacturing within biologics, biopharmaceuticals, or a regulated industry
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Familiarity with Good Manufacturing Practices (GMPs), 21 CFR Parts 210 and 211, biological regulations per 21 CFR Parts 600s, ICH Guidelines, and EU GMPs
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Knowledge and/or exposure to biological manufacturing processes including microbial and cell culture cell banking, fermentation/cell culture, purification, and fill/finish
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Ability to apply basic scientific and regulatory principles to solve operational and routine quality tasks
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Familiarity with electronic systems and ability to develop and produce reports using Microsoft products
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Creative individual with strong analytical, troubleshooting, and decision-making skills
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Ability to quickly learn new manufacturing processes supporting new clients
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Able to work in a team setting and independently under supervision
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Ability to deliver results in a fast-paced environment to meet client deadlines
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Knowledge of LIMS, Master Control, and Trackwise systems preferred
The anticipated salary range for this position in MD is $105,000 – $120,000 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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