QC Chemist

Tampa, FL

Posted: 08/12/2019 Job Number: JN -082019-11038
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: Tampa, FL
Industry: Pharmaceutical
Hours: Monday-Friday, 8am-5pm
Salary: $22.00/hr-$32.00/hr depending on skillset
Employment Type: Contract up to 6 months

Environment: This client is one the world s leading suppliers to the pharmaceutical, biotech and specialty ingredients markets. We create products that support a healthier lifestyle and enhance ones quality of life. Isn t this a company you want to work for?


Work cross functionally within the department to provide routine testing to support the successful completion of various projects.

Essential Functions:
  • Independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines.
  • Work with word processing, spreadsheets and data analysis
  • Handle math calculations, i.e., be able to calculate percentages, free acid/base equivalents from a salt, work with equations necessary for method validations work, etc.
  • Gain ability to do routine analysis of data and begin to review others work
  • Document all work in a laboratory notebook following cGMP guidelines
  • Follow company written policies and procedures, including all appropriate SOPs
  • Develop a proficiency in how to operate the instrumentation and work with Empower software
  • Ability to work on multiple projects and meet all project deadlines
  • Maintain a clean and safe laboratory work environment
  • Develop an understanding of compliance regulations
  • Compare data to specifications
  • Develop an understanding of Out of Tolerance and Out of Specification situations
  • Write and review documents including SOPs, deviation reports, change controls and test methods
Requirements:
  • Minimum 1-3 years of cGMP experience within pharmaceuticals or related industry
  • Experience with HPLC, GC and dissolution testing highly desired
  • Experience with wet chemistry, UV/IR/AA
  • Stability testing, Empower is a plus
  • Minimum AA/AS degree (Bachelor s degree preferred) with minimum 1-3 years of relevant experience
  • Maintain a positive, professional and confidential relationship with internal and external clients
  • Demonstrate good oral and written skills
  • Eager to learn, works independetly and as team player
EOE/ADA
Search words: QC, quality control, Chemist, Scientist, pharmaceuticals, HPLC, GC, Dissolution, stability testing, Empower, lab assistant, UV/IR/AA, wet chemisty
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