OPEN JOB: Quality Control Scientist (Pharma) LOCATION: Danbury, Connecticut ****Working Hours: 12:30pm to 9pm, Tuesday to Saturday. Additional stipend earned for working Evening Shift and Saturdays. SALARY: $77,600 to $105,000 BENEFITS - Full RELOCATION ASSISTANCE AVAILABLE INDUSTRY: Pharmaceutical JOB CATEGORY: Manufacturing - Quality - 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.
Essential duties - 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.
REQUIRED: - 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
If you are interested in pursuing this opportunity, please respond back and include the following:
- MS WORD Resume
- required compensation.
- Contact information.
- Availability
Upon receipt, one of our managers will contact you to discuss the position in full detail.
JASON DENMARK Recruiting Manager INTERMEDIA GROUP, INC. EMAIL: ...@intermediagroup.com LINKEDIN: VISIT OUR FULL LIST OF OPEN POSITIONS: