Associate QC Scientist Position Summary Shift: Monday-Friday 12am-8:30am 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life‑cycle supply. With time‑tested experience in development sciences, delivery technologies, and multi‑modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life‑enhancing and life‑saving treatments for patients annually. This Associate QC Scientist is responsible for Environmental Monitoring sampling, analyzing, and aseptic monitoring and microbiological testing to support Phase I/II GMP manufacturing. Works in a fast‑paced environmental supporting the quality control department of a CMO for manufacturing of biologic bulk drug substance, sterile finished drug product, and fill/finish. The role Perform Environmental Monitoring in Cleanrooms, including sampling of viable surfaces, viable air and non‑viable particulates in a Phase III/Commercial GMP Manufacturing facility. Conduct routine sampling and testing of Clean Utilities such as USP water (WFI) and clean steam along with conducting bioburden testing on prepared buffers/solutions, equipment cleaning samples, in‑process and release drug product samples. Isolate and sub‑culture microorganisms for identification. Provide input on SOP revisions and may assist in the creation and editing of protocols. Work closely with manufacturing and QA to coordinate routine EM, changeover EM, and monitoring to support client campaigns, effectively communicating results through discussion and documentation. Perform Aseptic Process Simulations (media fills) and fill/finish monitoring which includes continuous monitoring of air quality, personnel aseptic technique, and environment integrity. Compile and trend Environmental Monitoring data for reporting purposes. The candidate B.S. or A.S. in a Life Sciences discipline and 0‑4 years of relevant experience working in cGMP cleanrooms. Experience working in cGMP Quality Control – Good Manufacturing Practices (cGMP’s). Flexibility in following unique campaign requirements that may include off‑hour and weekend work. Experience with Microsoft Excel and Microsoft Word; strong exposure and attention to detail in revising SOPs and analyzing data. Have knowledge and ability to apply basic scientific and regulatory principles to solve operational and routine quality tasks. Ability to produce results in a fast‑paced environment to meet client deadlines under minimal supervision. The anticipated salary range for this position in Maryland is $58,240 - $80,080 plus an annual bonus target. 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, industry, skill set, education, and business needs. Why you should join Catalent Competitive medical benefits and 401K 152 hours PTO + 8 paid holidays Dynamic, fast‑paced work environment Opportunity to work on continuous improvement processes 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, including the job number, title, and location to . 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. 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 for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE. #J-18808-Ljbffr