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Quality Control Supervisor buy in US, Free Classifieds Ads

Company Name:
Nexgen Pharma
Bachelors or higher degree in Chemistry or related discipline. 10 + years experience in an analytical chemistry laboratory.
5 + years experience in GLP or GMP (preferred) environment. 5 + years experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC and dissolution apparatus. Demonstrated ability to act in a Lead capacity and provide direction to others. Ability to build relationships at all levels of the organization. Strong communication and demonstrated listening skills. Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision.
Strong attention to detail.
Supervise the daily activities of the QC laboratory by establishing testing priorities and schedules and assignments of staff. Provide daily direction, guidance and feedback to staff based work priorities and schedules. Assure appropriate review of analytical results commensurate with Nexgen review policy. Supervise laboratory investigations. Maintain equipment calibration schedule and ensure that all required calibrations and maintenance are completed in a timely fashion. Author standard operating procedures and assist with revision process of current procedures. Ensure laboratory compliance with applicable regulations. Assist with procedural, cGMP, and safety training of laboratory staff
Act as communication liason for laboratory with other facility departments. Serve as backup for laboratory manager in his/her absence. Ensure timely and accurate method transfers from method development group. Perform analytical testing of raw materials, in-process samples, and finished products using analytical laboratory instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC and dissolution apparatus as necessary. Assist with preparations for internal and external laboratory audits and inspections.
Other related duties as required.
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