The Analytical Chemist role will include the following responsibilities:
Carry out responsibilities in accordance with the Safety, Health and Welfare at Work Act 2005 and to implement appropriate safety procedures in the Laboratory.
Responsible for performing sample preparation and analysis procedures, stability & validation testing, completing all documentation, review results, troubleshooting any problems and all other laboratory related duties as assigned and required.
Identification and delivery of improvements in efficiencies within the analytical laboratory through the implementation of new laboratory systems, processes and reporting tools.
Interpretation of data output to determine conformance with product specifications and peer review of data to determine conformance with product specifications.
Strong instrumentation experience such that analysis is performed with minimal error and based upon GMP/procedural knowledge, ability to recognize laboratory technique or instrumental events that could impact the integrity of the test data.
Responsible for support of validation activities e.g. process qualification, instrument qualifications, method transfer / validation etc.
Requirements:
Degree in Analytical Chemistry or relevant Science degree.
Relevant experience in a laboratory /quality environment within the Pharmaceutical Industry.
Experience using a Laboratory Information Management System and Chromatography Data System is essential.
Excellent IT Skills.
Experience implementing Lean, 6d or 5S type systems would be an advantage.
Strong team player with ability to lead and influence.
Strong Implementer with a proven track recor
Ability to work on own initiative and with little supervision..
Package:
Contract rate - Negotiable based on eJob Description
The Analytical Chemist role will include the following responsibilities:
Carry out responsibilities in accordance with the Safety, Health and Welfare at Work Act 2005 and to implement appropriate safety procedures in the Laboratory.
Responsible for performing sample preparation and analysis procedures, stability & validation testing, completing all documentation, review results, troubleshooting any problems and all other laboratory related duties as assigned and required.
Identification and delivery of improvements in efficiencies within the analytical laboratory through the implementation of new laboratory systems, processes and reporting tools.
Interpretation of data output to determine conformance with product specifications and peer review of data to determine conformance with product specifications.
Strong instrumentation experience such that analysis is performed with minimal error and based upon GMP/procedural knowledge, ability to recognize laboratory technique or instrumental events that could impact the integrity of the test data.
Responsible for support of validation activities e.g. process qualification, instrument qualifications, method transfer / validation etc.
Requirements:
Degree in Analytical Chemistry or relevant Science degree.
Relevant experience in a laboratory /quality environment within the Pharmaceutical Industry.
Experience using a Laboratory Information Management System and Chromatography Data System is essential.
Excellent IT Skills.
Experience implementing Lean, 6d or 5S type systems would be an advantage.
Strong team player with ability to lead and influence.
Strong Implementer with a proven track recor
Ability to work on own initiative and with little supervision..
Package:
Contract rate - Negotiable based on e
We need : English (Good)
Type: Permanent
Payment: package
Category: Pharmaceutical