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Analytical Quality Control Chemist III

Clearwater, FL

Posted: 02/14/2021 Job Number: JN -022021-12526

Job Description

Analytical Quality Control Chemist III

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 III
  • Location: Clearwater, FL
  • Industry: Pharmaceutical (GMP environment)
  • Salary: Up to $32/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:
  • Designs, executes, and interprets complex procedures and protocols within a project or goal, subject to approval of supervisor.
  • Trains and directs lower level personnel.
  • Writes SOP s and protocols.
  • Reduces literature references to practices
  • Works independently on execution of complex procedures and methods
  • Demonstrates ability to accurately record and review laboratory documentation generated from developmental as well as established procedures.
  • Influences purchase of laboratory supplies as well as capital equipment.
  • Suggests alterations to procedures and protocols and studies. Compliant with safety and hazardous waste procedures.
  • Participates in moderate to extensive problem solving which requires original thought. Prepares reports with interpretation and can interpret the results of complex experiments.
  • Non-routine assignments. Designs experiments when requested. Handles major portion of project activity with supervision.
  • Performs routine as well as more complex assays and preparations.
  • Troubleshoots equipment, laboratory protocols and procedures.
  • Participates in audits for regulatory requirements.
  • Treats data with a high level of integrity and ethics.
  • Conscientious with safety procedures and knowledgeable of hazardous waste procedures.
  • Performs other related duties as assigned by management.

Qualifications
  • Minimum 8 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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