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Analytical Quality Control Chemist II

Clearwater, FL

Posted: 02/14/2021 Job Number: JN -022021-12525

Job Description

Analytical Quality Control Chemist II

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 federal contracting 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: Analytical Quality Control Chemist II
  • Location: Clearwater, FL
  • Industry: Pharmaceutical (GMP environment)
  • Salary: Up to $28/hr.
  • Employment Type: Contract with the possibility to go permanent
Client Overview
A dynamic pharmaceutical technology company that empowers its employees with responsibility and offers a supportive and highly progressive work environment. This company is a contractor development manufacturing organization environment that is fast-paced and mainly focuses on oral solid dosage.


Overview:
Provides support for the general operation of the laboratory such as preparation of laboratory solutions, conducting basic chemical biological reactions, preparations and tests.

Responsibilities:
  • Works independently on execution of procedures and methods.
  • Assists scientists and other laboratory personnel in design and interpretation of experiments or project (goal).
  • Performs routine as well as more complex assays and preparations.
  • Troubleshoots equipment, laboratory protocols and preparations
  • Accurately records and reviews laboratory data generated from established methods and procedures
  • Treats data with a level of integrity and ethics
  • Maintains laboratory supplies of day to date materials and chemicals
  • Conscientious with safety procedures and knowledgeable of hazardous waste procedures
  • Performs other related duties as assigned by management

Qualifications
  • Minimum 5 years experience in a cGMP pharmaceutical or related environment
  • BS Degree with a scientific discipline
  • Experience with wet chemistry, HPLC, GC, Dissolution
  • Raw material, in-process and finished product testing
  • Stability testing is a plus
  • Must be able to speak clearly, read, write and understand the English language.
EOE/ADA

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