Job DescriptionPosition Overview: Catalent hires people with a passion to make a difference to the health of millions of people globally. Your expertise, coupled with Catalent's advanced technologies and collaboration with thousands of innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. Interested in learning more about life at Catalent? Start hereJob TitleLead Quality Control Technician - Critical Reagents/AliquotingCatalent Gene Therapy is looking to hire a Lead Quality Control Technician to support our growing team in Baltimore, MD (BioPark).The Lead QC Technician will maintain inventory of reference standards & critical reagents as well as receive reference standards and critical reagent materials. Primary contact for multiple departments for inquiries regarding status of aliquoting requests.The Lead QC Tech must demonstrate technical knowledge,be familiar with basic scientific/regulatory principles, possess initiative, and maintain a strong commitment to scientific excellence.Catalent Cell & Gene Therapy is a premier development and manufacturing organization supporting the pharmaceutical and biotechnology industries. Catalent focuses on bringing client drug compounds from discovery to the clinic with services that include analytical development, pre-formulation testing, formulation development, GMP manufacturing and stability storage and testing.The Role Manage the entry and tracking of reference standards and critical reagents associated to lots including the preparation of labels and label vials for samples & coordinate and execute sample transfer to various departments.Lab duties including reconstitution and aliquoting of samples requiring strong pipetting and aseptic technique.Receive and send shipments for samples, reference standards and critical reagents.Reconstitution and aliquoting of reagents.Works closely with Manufacturing for scheduling of samples submission to the QC lab. May also interact with Project Managers on sample coordination.Assist in preparing of samples for shipment to contract laboratories.Assist with QC reagent preparation.Perform laboratory cleaning as part of routine work.The Candidate BS or AS in a Life Sciences discipline preferred and a minimum of 2 years of relevant experience working in a cGMP environment.Strong pipetting and aseptic technique.Experience with MS Excel and Word for tracking of testing.Experience working in a Phase III / Commercial Manufacturing setting preferred.Have the knowledge and ability to apply basic scientific and regulatory principles to solve operational and other routine quality tasks.Strong attention to detail and strong organizational skills along with strong written and verbal communication skills.Familiarity with Good Manufacturing Practices (cGMP's).Flexibility with hours/scheduling due to business need.Catalent's Standard Leadership Competencies Leads with Integrity and RespectDelivers ResultsDemonstrates Business AcumenFosters Collaboration and TeamworkChampions ChangeEngages and InspiresCoaches and DevelopsPosition BenefitsJoin a high growth and fast paced organization with a people focused cultureGlobal exposure, defined career path and annual performance review and feedback processCompetitive Medical, Dental, Vision and 401KCatalent 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.Catalent is committed to the health and safety of its employees, visitors and the customersand patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.personal initiative. dynamic pace. meaningful work.Visit www.catalent.com/careers to explore career opportunities.Catalent is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation or gender identity. 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 US 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.