Position Description

Analytical Chemist (Pharmaceutical/ Tuas/ 1-year contract)
Job Code 16320
Division GMP TECHNOLOGIES (S) PTE LTD (EA Licence:11C3793)
Job Placement Location Singapore
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Responsibilities

  • Supervise, develop, and motivate laboratory analyst to help realize their maximum potential so as to contribute towards achieving the objectives of the department.  Provide technical training on laboratory instrumentation to laboratory analysts.
  • Ensure that all data supporting the resolution of process and method issues have sufficient accuracy to allow for the correct actions to be taken to address the issue.
  • Contribute to the formulation and development of the plans for the implementation of new testing technologies and methods.
  • Ensure a safe working environment for the laboratory through participating or issuing safety risk assessment for product specific methods, or techniques or material and performing 6S inspection.
  • Assist Laboratory Operation Manager in supporting laboratory budget management and Analytical Laboratory resource planning.
  • Involve in the approving change that may have an impact on product quality, validation and/or cGMP compliance.  This may require assessment of testing requirement, co-ordinate testing of samples and comment on change documentation and ensure closure of change.  Upon completion, review and ensure closure of changes.
  • Draft, compile, review and update appropriate laboratory documents such as testing protocol, procedures and guidelines relating to GMP and operational framework of the laboratory.
  • Lead or participate in investigation arising from laboratory investigation, incidents and accurately assess the impact of the failure so as to make appropriate recommendations remedial actions for follow-up.

 

 

Requirements

  • At least a degree in chemistry.
  • At least 1-4 years’ experience in an analytical environment, preferably in the pharmaceutical industry.
  • GMP and GLP knowledge
  • Knowledge of laboratory instrumentation (ie HPLC, GC)
  • LIMS and corporate ERP system knowledge
  • Regulatory requirements for method validation.

 

To find out more about this opportunity, please contact Lionel Liew at lionel.liew@gmprecruit.com.

GMP Technologies (S) Pte Ltd   |   EA Licence: 11C3793 |   EA Personnel: Lionel Liew   |   Registration No: R1330693

 

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