Analytics Associate Scientist II

Catalent Pharma Solutions•Kansas City, MO

1d•Onsite

About The Position

The Analytics Associate Scientist II 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. The Role: 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. Other duties as assigned.

Requirements

Bachelor's degree in related life science or physical science required.
Hands‑on experience operating HPLC and Karl Fischer (KF) preferred.
Proactively identify and address work‑related issues at both the individual and team level.
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form along with communication skills (written and verbal) with internal and external customers.
Basic understanding of instrument operations and troubleshooting skills in multiple techniques.
Well organized and ability to multitask as well as efficient time management.

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.
Other duties as assigned.