Scientist 1, Analytical Development

Scientist 1, Analytical Development Position Summary Work Schedule: Monday-Friday, core hours 8am-4:30pm 100% on-site (San Diego) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Catalent’s San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic. This facility offers an array of services that support oral and injectable dosage forms that include preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego location is the home of our Catalent Spray Drying technologies with downstream roller compaction capabilities to support the needs of our client’s most challenging compounds. The Scientist 1 in our Analytical Development group will independently plan and execute simple laboratory experiments and clearly communicate the status of projects to cross‑functional team members, management, and clients. This individual will support the qualification of analytical test methods for Active Pharmaceutical Ingredients (API), intermediates, and final drug products using a variety of chromatography techniques (H/UPLC, GC), physical characterization techniques (TGA, DSC, PXRD, GVS, SEM) and dissolution/water content methods. You will be a key member of a multi-site mission to deliver unparalleled service to our clients and quality drug products to the patients. The Role Perform and train others on a variety of analytical techniques including analytical balances, pH meters, HPLC/UPLC, UV/Vis spectroscopy, GC, USP dissolution testing apparatus, moisture analysis by Karl Fischer, disintegration, Pion µdiss, DSC, TGA, PSD, PXRD, SEM, hardness, and friability testing. Develop cleaning verification methods and execution of excipient compatibility and forced degradation studies, under supervision. Troubleshoot and optimize analytical methods for characterization of drug products and intermediates. Perform qualification studies to determine if methods are suitable for transfer to Quality Control. Simple experimental design and execution will be performed independently. Complex design may need supervisor assistance. Data interpretation should be conducted with limited guidance. Identify key factors from data and understand their importance. Clear and accurate record keeping in laboratory notebooks and some secondary review of other colleagues’ work for scientific accuracy and compliance. Increase client interaction. Individuals may lead discussions with clients on technical topics relating to their project. Individuals should have a good general foundation of scientific principles, chemistry concepts, and be proficient in core analytical scientific techniques, GMPs and technical writing. Other duties as assigned. The Candidate Bachelor’s degree of Science required plus a minimum of one (1) year of analytical development experience. We will also accept a Master’s of Science without any formal industry experience, but highly preferred to have two (2) years of experience in analytical development. The individual must have demonstrated proficiency in the qualification of analytical test methods for API, intermediates, and final drug products, particularly HPLC and UPLC stability‑indicating assays, GC, dissolution methods, and water content methods. The individual should also have experience in physical characterization techniques such as TGA, DSC, PXRD, GVS, and SEM. The individual will be responsible for developing product‑specific cleaning methods to support use of GMP manufacturing equipment. Physical Requirements: Individual needs to be accessible to lab and office staff and able to use required office equipment. Specific vision requirements include reading of written documents and use of computer monitor screen frequently. Pay The anticipated salary range for this role in California is $78,000 to $85,000 annually. 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. Why you should join Catalent Amazing employee activities: Movie Day, Monthly Birthday Celebrations, Friday Bagel Breakfast, On‑site Fitness Center with machines, Sponsored Sports Teams, and several other company-sponsored events that encourage positive employee comradery, which contributes to effectively building positive employee relationships, overall creating a positive work environment. Environmentally friendly green initiatives with on-site practices as well as regularly participating in Beach Clean‑up activities for community engagement. Defined career path and annual performance review and feedback process. Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives. Several Employee Resource Groups focusing on Diversity and Inclusion. Competitive salary with bonus potential. Generous 401K match and Paid Time Off accrual. Medical, dental and vision benefits effective day one of employment. 152 hours of PTO + 10 paid holidays. Positive and fast‑paced working environment focusing on continually improving processes to remain innovative and dynamic. Tuition Reimbursement – Let us help you finish your degree or earn a new one! WellHub program to promote overall physical wellness. Perkspot – offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories. 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, confirming your request for an accommodation and including 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. #J-18808-Ljbffr Catalent Pharma Solutions