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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 I
Clearwater, FL
Posted: 02/14/2021
2021-02-14
2021-03-28
Job Number: JN -022021-12524
Job Description
Analytical Quality Control Chemist I
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
EOE/ADA
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 I
- Location: Clearwater, FL
- Industry: Pharmaceutical (GMP environment)
- Salary: Up to $24/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:
- Expected to follow routine procedures and protocols under close supervision
- Documents findings in written form per SOP
- Requires close to moderate supervision on a day to day basis. May have demonstrated ability to act independently as situations allow
- Demonstrates some problem solving and troubleshooting ability related to routine procedures
- Works effectively as part of a research team. Demonstrates a cooperate attitude
- Normally receives general instructions on routine work, detailed instructions on new assignments
- Performs tasks accurately, conscientiously and reliably
- Able to communicate clearly to colleagues and clients in both written and verbal form
- Performs other related duties as assigned by management
Qualifications
- Minimum 1-3 years experience in a cGMP pharmaceutical or related environment
- BS Degree with a scientific discipline
- Experience with wet chemistry, HPLC, GC, Dissolution
- Stability testing is a plus
- Must be able to speak clearly, read, write and understand the English language.
EOE/ADA
