Analytical Bench Chemist
- Contractor
- Full-Time
- Charles City, IA
- Splintpharma
- Prefferd visa: OPT, CPT, F1, H4, Have H1 Visa, Need H1 Visa, EAD
- Posted 1 year ago – Accepting applications
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Offerd Salary $ 30 - $ 45
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Required Position 2-4 hires
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Experience 0-3 Years Required
Client: Cambrex Pharmaceuticals
Analytical Bench Chemist LOA: 12 months (plus 1 year extension, after initial 12 months), Charles City, IA
Bulk API Manufacturing
Consultant will be required but not limited to the following:
Perform a wide variety of analytical chemical analyses for release of raw materials, intermediates and small molecule API drug substance with a proven ability in general wet chemistry and chromatography (HPLC, UPLC, GC)
Perform instrument maintenance and troubleshoot equipment as needed
Perform method development including instrument parameters, new instruments and method improvement studies
Adhere to all EPA, FDA, cGMP and DEA regulations and internal SOPs as they relate to the operation of the Quality Control lab and general operation of the chemical production facility.
Responsible for coverage of all job duties typical for analytical method development and validation
Experience with Wet Chemistry, Chromatography (HPLC, UPLC, GC) -MUST, cGMP Regulation knowledge – PREFERRED
Experience in small molecule environment, Extensive knowledge of analytical instrumentation - PREFERRED
Very busy, Growing fast.
Client: Cambrex Pharmaceuticals
Analytical Bench Chemist LOA: 12 months (plus 1 year extension, after initial 12 months), Charles City, IA
Bulk API Manufacturing
Consultant will be required but not limited to the following:
Perform a wide variety of analytical chemical analyses for release of raw materials, intermediates and small molecule API drug substance with a proven ability in general wet chemistry and chromatography (HPLC, UPLC, GC)
Perform instrument maintenance and troubleshoot equipment as needed
Perform method development including instrument parameters, new instruments and method improvement studies
Adhere to all EPA, FDA, cGMP and DEA regulations and internal SOPs as they relate to the operation of the Quality Control lab and general operation of the chemical production facility.
Responsible for coverage of all job duties typical for analytical method development and validation
Experience with Wet Chemistry, Chromatography (HPLC, UPLC, GC) -MUST, cGMP Regulation knowledge – PREFERRED
Experience in small molecule environment, Extensive knowledge of analytical instrumentation - PREFERRED
Very busy, Growing fast.