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 experienceAt least 4 years' experience in a laboratory setting, preferably in pharma3-5 years' experience in quality control systemsGood written communication skillsUnderstanding of GMPs and regulatory guidelines as they relate to the pharmaceutical products preferredAccess, Excel, Word and Power Point skillsIf you are interested in pursuing this opportunity, please respond back and include the following :
MS WORD Resumerequired compensation.Contact information.AvailabilityUpon receipt, one of our managers will contact you to discuss the position in full detail.
JASON DENMARK
Recruiting Manager
INTERMEDIA GROUP, INC.
EMAIL : jdenmark@intermediagroup.com
LINKEDIN : https : / / www.linkedin.com / in / jasondenmark
VISIT OUR FULL LIST OF OPEN POSITIONS :
https : / / intermediagroup.catsone.com / careers
Salary : $77,600 - $105,000
