Job Description
Principal Activities:
- Be able to articulate work related issues clearly and effectively to management and peers
- Performs accurate routine testing utilizing instrumental methods of analysis (HPLC, GC, FTIR, UV, ICP-MS) with emphasis on chromatography to meet departmental objectives
- Updates and routes SOPs, MOAs, Specifications through Documentum as delegated by supervisor for USP compliance
- Provides technical support for method validation, verification, transfers, evaluations
- Performs troubleshooting of instrumentation by applying problem solving skills and sourcing out literature or vendors, if necessary
- Provides guidance to Associate Scientist personnel on topics such as GMP, safety, antineoplastic and new employee training
- Maintains accurate records of all work performed with respect to a given project. Documents testing in compliance with GDP
- Manages work and time based on departmental priorities using own judgement and objective reasoning
- Performs peer review of data to ensure compliance and accuracy
Requirements: - Possess a BS degree in Chemistry or Biology, or equivalent physical science
- Typically, 1-4 years of related experience in pharmaceutical industry and a familiarity with cGMP and FDA regulations
- Must have hands-on experience and knowledge of chromatographic methods and related chromatography data systems (i.e. Empower)
- Must be proficient in Microsoft Office
- Some method development experience and extensive troubleshooting knowledge is highly desirable
- Must be flexible with continually changing projects and priorities
Pay ranges between $28-34/hr based on experience
Job Tags
Contract work, Flexible hours,