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The Staffing Resource Group, Inc
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http://www.srg-us.com
http://www.srg-us.com
Analytical Quality Control Chemist II
Clearwater, FL
Posted: 02/14/2021
2021-02-14
2021-03-30
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.
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:
Qualifications
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
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.
