
Scientist III, Quality Control
- Danbury, CT
- $80,000-120,000 per year
- Permanent
- Full-time
- 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 5+ years related experience or an equivalent combination of training and experience
- At least 5+ years' experience in a laboratory setting, preferably in pharma
- 5+ years' experience in quality control systems
- EMPOWER experience is required
- Good written communication skills
- Understanding of GMPs and regulatory guidelines as they relate to the pharmaceutical products preferred
- Good interpersonal skills
- Access, Excel, Word and Power Point skills