Quality Control Senior Associate Scientist I

Position Summary Quality Control Senior Associate Scientist I responsibilities include ensuring compliance with site SXPs, corporate policies, and EHS requirements while executing assigned tasks according to established procedures. The role is 100% on‑site at Catalent’s Kansas City (KCM) facility and operates on a Tuesday through Saturday schedule (8:00am–4:30pm). Responsibilities Execute testing procedures for raw materials, stability, and drug products, including HPLC, GC, Karl Fischer, particle size, ICP‑MS, FT‑IR, and dissolution. Develop and execute laboratory work plans and schedules with input from supervisors or senior team members. Maintain high‑quality documentation in accordance with regulatory guidance and site SOPs, using notebooks, forms, and other required tools. Perform procedures or methods of moderate and advanced complexity with accuracy and completeness, reviewing own work for quality. Identify and remediate minor quality or compliance gaps during lab work with minimal guidance. Develop or validate methods of moderate and advanced complexity as needed. Draft technical documents such as methods, specifications, and certificates of analysis with little to no guidance from a supervisor. Participate in or draft events related to deviations and investigations. Review routine laboratory documentation and perform peer reviews. Train others on procedures and lab techniques and assist with efficiency and compliance improvement projects. Perform all other duties as assigned. Qualifications Bachelor’s degree in a related life science or physical science field with a minimum of 2 years of related work experience, or Master’s degree with 1 year preferred. Experience with HPLC is required (Empower experience preferred); prior GMP experience is strongly desired. Ability to process, maintain, interpret, and analyze data with a basic understanding of instrument operation and troubleshooting across multiple techniques. Strong written and verbal communication skills, with the ability to proactively identify and communicate barriers to management and resolve challenges with minimal guidance. Physical Requirements & Work Environment Ability to stand, walk, or sit for extended periods; occasional lifting, pushing, and pulling up to 40lbs; frequent physical movements such as kneeling and reaching in a controlled warehouse environment with rare exposure to varying conditions (temperature, noise, humidity, hazards, vibration). Benefits 152 hours of PTO + 8 paid holidays Generous 401(k) match Medical, dental, and vision benefits effective day one of employment Tuition Reimbursement EEO Statement 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, please submit your request via email, including the job number, title, and location to View email address on click.appcast.io. #J-18808-Ljbffr Catalent Pharma Solutions