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Quality Control Manager buy in US, Free Classifieds Ads

Company Name:
Nexgen Pharma
REQUIREMENTS:
B.S. in Chemistry or related discipline, or equivalent combination for education and experience.10 + years experience in an analytical chemistry laboratory. 5 + years experience in GLP or GMP (preferred) environment with a strong commitment to the highest quality standards. 5+ years experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC, MS and dissolution apparatus. 5 + years supervisory and/or management experience with minimum staff of 10 + employees. Strong communication skills, both written and verbal. Experience with software-controlled LIMS systems.
Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision. Demonstrate positive qualities of effective leadership, daily staff engagement and conflict resolution. Strong attention to detail.
JOB DUTIES:
Direct the daily activities of the Quality Control laboratory (analytical and microbiological) based on company priorities and objectives to ensure incoming raw materials, retest materials, and in-process and finished nutraceutical and pharmaceutical products are tested in a cGMP compliant manner within production timelines. Prepare and administer annual laboratory budget. Ensure laboratory compliance with cGMPs and prepare laboratory for internal and external audits and inspections. Accountable for laboratory staff, including direct management of laboratory supervisor and other exempt personnel.
Ensures training, timely feedback, regular and annual reviews are provided and appropriate merit increases are recommended for non-exempt and exempt personnel. Actively participate in production, quality unit, and management meetings. Serve as scientific liaison to other facilities and departments and scientific/quality control member of Material Review Board. Author standard operating procedures, analytical test methods, protocols (equipment qualifications, method validation, stability, etc.), and corresponding reports. Review and approve laboratory investigations, corrective and preventive actions, change requests, and deviations as necessary. Ensure proper handling, storage, usage, and disposal of laboratory chemicals and equipment with all applicable state and federal laws. Assist with review of completed raw material and product specification forms for material and product release from QC. Other related duties as required.
Please submit your cover letter and resume to:
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