Quality Control Scientist (Pharma) - Danbury, Connecticut (relo) $77,600 to $105,000

• Provides general support to maintain quality control systems within the company. 
• Ensures that performance and products conform to established company and regulatory standards. 
• Analyzes finished formulations, raw materials, in process materials, or stability samples by HPLC/GC, in support of the company’s quality program. 
• Interprets and evaluates the analyses in terms of accuracy and precision and recommends corrective action where necessary.
• Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation. 

• Conduct routine and non-routine HPLC/GC analysis of raw materials, in process, and finished formulations according to standard operating procedures.
• Perform chemical analyses of product to ensure stability.
• Compile data for documentation of test procedures that may include microbiological and/or chemical assays, stability program testing and formulation studies.
• Calibrate and maintain lab equipment.
• Participate in the preparation of investigations, summaries and reports.
• May assist in developing testing methods.
• Review data obtained for compliance to specifications and report abnormalities.
• Revise and update standard operating procedures as needed. 
• May perform special projects on analytical and instrument problem solving. 
• Applies knowledge of good manufacturing practices, good laboratory practices and good record keeping practices on a daily basis.
• Follows written test methods and protocols. 
• Process data, report data and prepare tables and graphs for the completed testing.  Identify problems, e.g. out of trend data.  Professional interactions are primarily within the QC organization.
• Responsible for observing all Company, Health, Safety and Environmental guidelines.

• BS Degree in a scientific discipline with 2 to 4 years' experience or MS or MBA 1 to 3 years or related experience or an equivalent combination of training and experience
• At least 4 years' experience in a laboratory setting, preferably in pharma
• 3-5 years’ experience in quality control systems
• Good written communication skills
• Understanding of GMPs and regulatory guidelines as they relate to the pharmaceutical products preferred
• Access, Excel, Word and Power Point skills

• MS WORD Resume
• required compensation.
• Contact information.
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Salary : $77,600 - $105,000