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About Anchor Technical Services:
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Full service technical staffing firm specializing in the following:
IT
Engineering
Scientific
Communications
Click here to go to the Anchor Technical Services website.
For details about Anchor Technical Services, click here.
About the Opportunity/Requirements:
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As the Chemist II/QC Analyst, you must provide expertise in the development and revision of laboratory procedures. Be able to perform chemical analysis of developmental products (Pharmaceutical Analysis), raw materials, in-process and finished products using multiple complex test methodologies. Be available as a resource for all lab related activities. Participating in the development and execution of test method qualification protocols is necessary.
• Provide expertise for the writing and revising of laboratory procedures.
• Apply intermediate to advanced skills in various scientific techniques, principles, problem solving, organization of work and cost savings.
• Analyze pharmaceutical dosage forms using HPLC dissolution testing, spectroscopy, and wet chemistry techniques.
• Provide intermediate to advanced level of analytical support for raw materials, in-process, pharmaceutical analysis and finished product testing (release and stability) for conformance to specifications/acceptance criteria.
• Perform data generation/interpretation.
• Perform method development/validation.
• Comply with company Procedural Guidelines, laboratory procedures, and safety procedures.
• Participate on Project/Product Management teams
• Provide guidance and training to laboratory employees.
• Contribute to a team-oriented, continuous improvement quality process.
• Perform routine laboratory maintenance tasks including the organization and cleaning of work areas, checking for expired reagents, standards, solutions, chemicals and hazardous waste.
Education and Experience:
• BS degree in Chemistry or closely related field, with the equivalent of 4+ years experience in a pharmaceutical laboratory setting.
• MS degree in Chemistry or closely related field, with the equivalent of 2+ years experience in a pharmaceutical laboratory setting.
• Intermediate knowledge in the use and theory of analytical laboratory instrumentation.
• Knowledge of HPLC and dissolution testing are desirable; method development and validation experience a plus.
• Demonstrated understanding of laboratory interactions and cGMP/quality control requirements.
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