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Description

Manage, coordinate and supervise human, technical and material resources to provide fast and accurate information of analytical results performed to raw materials, intermediate and finished goods, verify that specifications are met, through the application of GMP for its subsequent approval and complying with SAMASS requirements.

Required Education level

•Pharmacobiologist Chemist.

•Degree in Chemistry.

Minimum years of experience

1 year of experience:

•Personnel Management.

•Management of lab equipment.

•Laboratory analyses.

Knowledge in:

•Microsoft Office.

•Good Manufacturing Practices (GMPs)

•Good Laboratory Practices (GPLs).

Key Individual Accountabilities

1.Assure compliance and collaborate with the improvement of the Quality System and SAMASS for the approval of internal and external audits.

2.Assure the correct analysis of raw materials, intermediate and finished goods, within the established time, through daily and weekly reviews.

3.Control the process of chemical and microbiological analysis for an easy detection of deficiencies, to determine with certainty the conformity or nonconformity of the analyzed samples.

4.Keep the laboratory equipment in optimal conditions for use.

5.Provide information and get feedback from internal entities related to laboratory activities.

6.Comply and enforce the established Quality Policies and Procedures.

7.Verify that personnel keep their work area in appropriate conditions and implement specific corrective actions.

8.Daily verify the reports of  raw material, intermediate and finished goods of Synthesis and Fermentation plants.

9.Daily compare the results written in analyst’s Journals with the equipment reports and the system records.

10.Daily review of journals, logbooks and quality records.

11.Confirm the validation of analytical methods.

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