Quality Control Chemist II - The Staffing Resource Group, Inc
Clearwater, FL 33760
About the Job
Quality Control Chemist II
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.
Position Overview:
In this role, you perform QC analytical activities in a highly regulated GMP environment. Activities include but are not limited to analytical method development, method validation, raw material testing, in process, release, and stability testing. Draft protocols, reports and procedures for analytical test methods and validation. The QC Chemist II will be required to write or revise SOPs, analytical procedures, and analysis reports, at the discretion of quality control supervisory staff.
Responsibilities:
- Title: Quality Control Chemist II
- Location: Clearwater, FL
- Industry: Pharmaceutical (GMP environment)
- Salary: Up to $27/hr. depending on experience
- Employment Type: Direct Hire
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.
Position Overview:
In this role, you perform QC analytical activities in a highly regulated GMP environment. Activities include but are not limited to analytical method development, method validation, raw material testing, in process, release, and stability testing. Draft protocols, reports and procedures for analytical test methods and validation. The QC Chemist II will be required to write or revise SOPs, analytical procedures, and analysis reports, at the discretion of quality control supervisory staff.
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
- 2 years experience in a cGMP pharmaceutical or related environment
- BS/BA Degree with a scientific discipline
- Experience with wet chemistry, HPLC, GC, Dissolution
- Must be able to speak clearly, read, write and understand the English language.
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.
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Source : The Staffing Resource Group, Inc
