Senior Chemist
Company Name:
Placement Services USA, Inc.
Supervises Two Chemists and the Microbiology Department Chemist
Independently write SOPs and change control forms for operation of lab instruments.
Responsible for general SOP preparation and revision.
Independently develop methods for justification and validation according to FDA (USP), & EP requirements.
Responsible for the security of the controlled substance raw materials and product
With little to no supervision responsible for validation and calibration of FT / IR spectrophotometer (Jasco 4100)
Independently perform various analytical tests on stability samples
Review of method development and method verification and write the protocol
Review of method validation of new project
Review of method verification of compandial product as well as the raw material
Responsible for reviewing contract laboratories results, reports and raw data;
Responsible for Raw materials and Packaging materials receiving to release procedure.
Responsible of all Raw materials and Packaging materials Specification preparation and revision as per current USP / NF.
Responsible of all wet analysis related instruments Standard Operational Procedure preparation as per general chapters of USP / NF and manufacturers operational procedure.
Responsible for testing and handling of working standard/reference standard
Maintain, troubleshoot & calibrate various analytical instruments (Malvern Analyzer; HPLC; GC; FT-IR; UV-VIS; Auto titrator; KF titrator and Mass Spectroscopy)
Solicit and negotiates quotes with contract testing labs Business Development teams for raw material and finished product testing.
Negotiates quotes with the laboratory chemicals and reagent suppliers.
U.S. Master of Business Administration degree in International Business and 6 months experience as a Chemist or in the related occupation(s) of Officer Quality Control or Production Chemist. Experience to include, experience in developing methods for justification and validation according to FDA (USP), & EP requirements and maintaining troubleshoot & calibrate various analytical instruments (Malvern Analyzer; HPLC; GC; FT-IR; UV-VIS; Auto titrator; KF titrator and Mass Spectroscopy).
OR
Bachelors degree in Pharmacy (or its foreign equivalent) and 5 years experience as a Chemist or in the related occupation(s) of Officer Quality Control or Production Chemist. Experience to include, experience in developing methods for justification and validation according to FDA (USP), & EP requirements and maintaining troubleshoot & calibrate various analytical instruments (Malvern Analyzer; HPLC; GC; FT-IR; UV-VIS; Auto titrator; KF titrator and Mass Spectroscopy).
Please send us your resume via email at with reference #503042 in the subject line. Do not copy and paste your resume in the body email. Please attach it as a Word document. Thank you.Estimated Salary: $20 to $28 per hour based on qualifications.
Placement Services USA, Inc.
Supervises Two Chemists and the Microbiology Department Chemist
Independently write SOPs and change control forms for operation of lab instruments.
Responsible for general SOP preparation and revision.
Independently develop methods for justification and validation according to FDA (USP), & EP requirements.
Responsible for the security of the controlled substance raw materials and product
With little to no supervision responsible for validation and calibration of FT / IR spectrophotometer (Jasco 4100)
Independently perform various analytical tests on stability samples
Review of method development and method verification and write the protocol
Review of method validation of new project
Review of method verification of compandial product as well as the raw material
Responsible for reviewing contract laboratories results, reports and raw data;
Responsible for Raw materials and Packaging materials receiving to release procedure.
Responsible of all Raw materials and Packaging materials Specification preparation and revision as per current USP / NF.
Responsible of all wet analysis related instruments Standard Operational Procedure preparation as per general chapters of USP / NF and manufacturers operational procedure.
Responsible for testing and handling of working standard/reference standard
Maintain, troubleshoot & calibrate various analytical instruments (Malvern Analyzer; HPLC; GC; FT-IR; UV-VIS; Auto titrator; KF titrator and Mass Spectroscopy)
Solicit and negotiates quotes with contract testing labs Business Development teams for raw material and finished product testing.
Negotiates quotes with the laboratory chemicals and reagent suppliers.
U.S. Master of Business Administration degree in International Business and 6 months experience as a Chemist or in the related occupation(s) of Officer Quality Control or Production Chemist. Experience to include, experience in developing methods for justification and validation according to FDA (USP), & EP requirements and maintaining troubleshoot & calibrate various analytical instruments (Malvern Analyzer; HPLC; GC; FT-IR; UV-VIS; Auto titrator; KF titrator and Mass Spectroscopy).
OR
Bachelors degree in Pharmacy (or its foreign equivalent) and 5 years experience as a Chemist or in the related occupation(s) of Officer Quality Control or Production Chemist. Experience to include, experience in developing methods for justification and validation according to FDA (USP), & EP requirements and maintaining troubleshoot & calibrate various analytical instruments (Malvern Analyzer; HPLC; GC; FT-IR; UV-VIS; Auto titrator; KF titrator and Mass Spectroscopy).
Please send us your resume via email at with reference #503042 in the subject line. Do not copy and paste your resume in the body email. Please attach it as a Word document. Thank you.Estimated Salary: $20 to $28 per hour based on qualifications.
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