**Associate, Interior Materials Support** **Summary:** _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 (https://biologics.catalent.com/our-locations/north-america/baltimore-usa/) _. 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._ The purpose of the **IMSA** role is to coordinate the flow of materials inside the manufacturing clean space. This role was created to assist the manufacturing team with locating needed materials, schedule with the warehouse when materials are required, and troubleshoot material replacements by Item Request Forms (IRFs). Additionally, the IMSA will maintain the 999 material and chemical inventories. **This is a full-time on-site position,** **7am-7pm 2-2-3 rotation** **Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.** **The Role:** + Follow a defined process for checking manufacturing inventory locations and order replenishments from the supply chain team. + Coordinate timing with the supply chain team to receive materials upon transfer from warehouse to manufacturing. + Verify handoff with warehouse and confirm that all items are correct on the associated work order and escalate discrepancies to supply chain team. + Physically and electronically (via Inventory Transfer in JDE) transfer materials from staging to designated location on the manufacturing floor. + Maintain First Expired, First Out (FEFO) practices through use of flow directions during replenishment. + Perform routine FEFO maintenance by evaluating current inventory and alerting Manufacturing Team of upcoming expiry dates. + Assist MFG team in resolving material discrepancies including expediting urgent requests. + Assist with cycle counting of inventor in mfg locations. + Audit the min/max quantities in all Kanban locations. + Serve as a resource in manufacturing suites, supporting MFG by delivering materials and limiting movement in/out of cleanrooms. + Perform inventory adjustments, lookups, inquiries, general problem resolution, and troubleshooting in company ERP system. + Assist the manufacturing team in returning unused or extra materials issued to the work order, allowing them to be returned to stock or inventory for future use. **The Candidate:** + High School Diploma with a minimum of 2-4 years GMP Manufacturing experience, OR + Associate’s Degree in a scientific, engineering or biotechnology discipline with a minimum of 1-2 years related experience; coursework with biotechnology focus highly desirable OR + Bachelor’s Degree (BS/BA) from an accredited college or university with an emphasis in a scientific or engineering discipline and some relevant work experience + Basic knowledge of current Good Manufacturing Practices (cGMP’s). Working knowledge of all relevant safety procedures within the company. General understanding of most areas in Manufacturing and supporting functional groups. + Familiar with or experience with cGMP Biotech or Pharmaceutical operations preferred + Must be team-oriented (proactively builds healthy working relationships between peers, their department and other groups). + Able to fluently communicate in English. Exhibits excellent written and oral communication skills. + Possesses a basic knowledge of non-manufacturing functions such as QC, Regulatory, QA, and/or Materials Management. _The anticipated salary range for this position in Maryland is $38,000 to $55,000 plus shift differential and annual bonus, when eligible. 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._ **Position Benefits:** + Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives + 152 hours of paid time off annually + 8 paid holidays + Competitive salary with yearly bonus potential + Community engagement and green initiatives + Generous 401K match and Paid Time Off accrual + 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. Visit Catalent Careers (https://careers.catalent.com/us/en) 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 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. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE (https://cdn.catalent.com/files/legal/CCPA-Privacy-Notice-at-Collection-for-California-Employees-and-Applicants-English.pdf) .