QC Associate Scientist

St. Petersburg, FL

Posted: 01/18/2021 Job Number: JN -012021-12406

Job Description

QC Chemist:

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
  • Title: QC Chemist
  • Location: St. Petersburg, FL
  • Industry: Pharmaceutical
  • Hours: Monday-Friday; 8:00 am 5:00 pm
  • Salary: $20.00-$24.00 hour paid weekly with benefits options
  • Employment Type: Contract to Hire
Environment: This client manufactures thousands of pharmaceutical, biologic, consumer health and beauty products utilizing superior and innovative drug delivery technologies to improve their value to patients and consumers. Our customer believes in a Patient First culture putting patients at the center of their work to ensure the safety, reliable supply and optimal performance of our products. Isn t this the type of company you want to work for?

Job Scope:
  • Testing and analysis of pre-capsulation, stability, finished products, in-process materials, fill moisture, raw materials, and cleaning verification and validation samples according to the assigned specifications, methods and protocols
  • Performs analysis of finished products, validation samples, in-process materials and raw materials, moisture testing, Gas, Water and manufacturing environmental sampling and testing according to the effective Specifications, protocols, Methods and Compendial monograms
  • Cultivate and identify bacteria or other microorganisms isolated on selective and non-selective media
  • Maintains cultures according to ATCC and departmental Standard Operating Procedures
  • Performs identification of microorganisms using techniques such as API, Gram Stain
  • Prepares reagents, standards, Medias needed for analysis
  • May be required to work with potent and teratogenic compounds
  • Responsible for login of samples (routine and non-routine) into GLIMS database and logbooks
  • Required to perform basic statistics to support analytical testing
  • Helps receive, label and store receipts of solvents and analytical reagents
  • Logs results into GLIMS database
  • Verifies co-workers calculations in notebooks/logbooks and verifies results in reports and/or appropriate systems to check for accuracy and integrity of data.
  • Shares responsibility for the routine calibration of analytical equipment such as, but not limited to balances, pH meters, KF analyzers
  • Disposes of hazardous waste according to environmental regulations and company/departmental procedures
  • Files and maintains laboratory records following Good Manufacturing Practices and as directed through applicable SOPs
Skills Needed:
  • Bachelor s Degree in Chemistry
  • 3 5 years background in pharmaceutical separation science and in-depth experience with HPLC, GC, and CE
  • Must have industry experience in a GMP lab

QC chemist, GMP, FDA, Pharma, HPLC, Lab, GC, Validation

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