Niveau: Bio-Technical Research Manager

Type d’emploi: Full Time, Permanent

Expérience: 2 - 7 years

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le contenu du travail


1) Responsible for good manufacturing practices to be followed in each and every department of the company.

2) To conduct training on GMPfor employees on regular basis (once in three months) with help from personnel department.

3) To keep track of all SOPbeing maintained in different department.

4) To keep track of any changes being done in SOPat any level and maintain the ’Master Document File’ with him.

5) To help for Internal Auditing and for preparation of any external Audit.

6) To check plant hygienic conditions in reference with ’G.M.P.’ and inform concerned authorities for compliance.

7) To keep records of Non compliances and compliances after follow up for all

Internal and external audit.

8) Audit faced and knowledge of ISO - QMS, EMS, OHSAS, HCAAP, HALAL, URSA etc.



BSc / MSc with min 2 years of experience from Chemical / Pharmaceutical Industry
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Date limite: 20-06-2024

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MÊMES EMPLOIS

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