Chemist II; Quality Control

Position Summary The Chemist II is responsible for performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Technical Support) and documenting results in accordance with SOPs. The role includes analysis and disposition of commercial materials, stability, validation, investigation, and environmental samples as assigned. Job Type Full‑time Responsibilities Follow all laboratory SOPs concerning safety, chemical handling and storage, gowning, equipment use, cGMP, GDP, data integrity, DEA requirements, etc. Perform laboratory chemical analysis on raw materials, in‑process materials, and finished products using ICP‑OES/MS, UV‑Vis, Fluorescence, GC, HPLC/UPLC, titration, and other wet chemistry techniques. Execute assay testing, content uniformity testing, impurities analysis, method transfers, cleaning validation testing, and process/interpret data at a moderate level with minimal to no errors. Maintain a clean and organized laboratory working environment. Dispose of used/expired/excess chemicals, solutions, solvents, etc. in dedicated waste receptacles. Report well‑written, accurate and timely results. Review data, calculations, notebooks, and reports. Assist in laboratory investigations and process validation testing and protocol/report review as assigned. Maintain and troubleshoot laboratory equipment at a moderate level. Suggest improvements to existing testing methods when possible. Assist with routine metrology functions (instrument cleaning, preventive maintenance, calibration, verification). Monitor and assist with maintaining proper inventory levels of laboratory supplies. Assist with sample receiving, chemical inventory, document filing, housekeeping, etc. Ensure compliance with all safety policies and promote a safe work environment. Other responsibilities as assigned by Management. Requirements Education & Experience Bachelor’s degree in a science‑related field. Between 4–8 years of laboratory experience preferred. Skills, Knowledge, and Abilities Knowledge of laboratory chemistry and cGMPs. Proficiency in Microsoft Word, Excel, graph/chart creation, and databases. Proficiency with HPLC/UPLC, ICP, dissolution, IR, UV/VIS, and wet chemistry testing. Experience with analytical laboratory software. Ability to multitask and meet tight deadlines. Excellent organizational skills with attention to detail. Effective presentation of results. Capability to perform moderate‑level testing and troubleshoot moderate method issues with some guidance. Ability to independently troubleshoot moderate instrument issues and handle complex instrument issues under supervision. Physical Demands Required to sit and stand for long periods. Frequently reach with arms/hands up to 2 feet. Good hand‑eye coordination. Occasional walking and kneeling. Must lift and/or move up to 50 pounds. Requires close, distance, peripheral, color vision and ability to adjust focus. Requires use of arms, hands, and fingers for handling objects, tools, and controls. Includes stooping, kneeling, crouching, standing, bending, sitting, speaking, hearing, and climbing stairs. Work Environment Laboratory and production facilities with proximity to heavy machinery and pharmaceutical powders. May move between production sites/areas; regular travel required. Employee hours/schedule may change based on business needs and management discretion. Required presence in the laboratory for daily testing and collaboration with department leadership and peers. Supervisory Responsibilities None Personal Protective Equipment or Attire Required for Position Gowning as required by GMPs and/or SOPs. Pay Range $75,000 – $89,999 per year #J-18808-Ljbffr Contract Pharmacal Corp