Senior Associate Scientist I
About The Position
The Senior Associate Scientist I performs work that is varied and that may be somewhat difficult in character but usually involves limited responsibility. Some evaluation, originality or ingenuity is required. Follows established protocols and work plans. May be assisted by laboratory technicians/assistants. Comply with divisional and site Environmental Health and Safety requirements. Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions—from science and engineering to operations and logistics.
Requirements
- Bachelor's degree in related life science or physical science field with a minimum of 2 years of related work experience required OR Master’s degree in a related life or physical science required; no prior work experience required, though relevant educational laboratory experience is preferred.
- Hands‑on experience operating HPLC and Karl Fischer (KF) required.
- Proactively identify and address work‑related issues at both the individual and team level.
- 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 internal and external customers, combined with excellent organization, time‑management, and multitasking abilities.
Nice To Haves
- experience with GC, LC‑MS, disintegration, friability, and TGA testing preferred.
Responsibilities
- Execute laboratory work plans/schedules developed with input from a supervisor or senior team member.
- Sample types include in-process, release or stability.
- Techniques include HPLC, GC, Karl Fischer, Disintegration, Friability, Hardness, and appearance.
- Under direction, may perform method development, validation, and transfer activities.
- Maintain accurate and high-quality laboratory documentation in accordance with regulatory guidance and Site SOPs.
- May draft technical documents such as methods or certificate of analysis.
- Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance.
- Assists in execution of efficiency improvement projects with guidance.
- Trains others on laboratory techniques.
- All other duties as assigned.
Benefits
- 152 hours of PTO + 8 paid holidays
- Generous 401K match
- Medical, dental and vision benefits effective day one of employment
- Tuition Reimbursement
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
