Post: Executive Quality Assurance
RESPONSIBILITIES
Job Purpose
The Incumbent as a member of the Quality Assurance and Technical services Team is responsible for implementation and execution of allocated QA related systems and processes in accordance with the relevant SOPs.
Job Purpose
The Incumbent as a member of the Quality Assurance and Technical services Team is responsible for implementation and execution of allocated QA related systems and processes in accordance with the relevant SOPs.
POSITION RESPONSIBILITIES
1.Handling of Product / Packaging validations .
2.Handling of cleaning validation program at site.
3.Involve in Qualification activities, by executing IQ, OQ, PQ at site to support different functions.
4.Preparation of annual Validation Schedule & tracking of same through VMP. 5.Conducting Hold time Study of Equipment & Product manufactured at site.
6.Support In process Quality assurance functions.
7.Management of Change control related to validation & Qualification .
8.Tracking of CAPA & commitment
1.Handling of Product / Packaging validations .
2.Handling of cleaning validation program at site.
3.Involve in Qualification activities, by executing IQ, OQ, PQ at site to support different functions.
4.Preparation of annual Validation Schedule & tracking of same through VMP. 5.Conducting Hold time Study of Equipment & Product manufactured at site.
6.Support In process Quality assurance functions.
7.Management of Change control related to validation & Qualification .
8.Tracking of CAPA & commitment
ORGANIZATIONAL RELATIONSHIPS
1.Management Associates All Departments
2.Executive, Asst. Manager, Manager from All Departments
3.Functional Heads
1.Management Associates All Departments
2.Executive, Asst. Manager, Manager from All Departments
3.Functional Heads
Skills / Knowledge / Qualification / Experience
1.B. Pharm. / M. Pharm.
2.1 to 4 years of experience in a pharmaceutical manufacturing facility.
3.Exceptional understanding of GMPs
4.Exposure to regulatory audits - FDA, ISO, WHO, WHO Geneva etc.
1.B. Pharm. / M. Pharm.
2.1 to 4 years of experience in a pharmaceutical manufacturing facility.
3.Exceptional understanding of GMPs
4.Exposure to regulatory audits - FDA, ISO, WHO, WHO Geneva etc.
IN LINE WITH GOOD DEVELOPMENT PLANNING , IT IS RECOMMENDED THAT COLLEAGUES DISCUSS THEIR SUITABILITY AND/OR READINESS FOR A NEW POSITION AND THEIR DIRECT MANAGER PRIOR TO APPLICATION. COLLEAGUES ARE REQUIRED TO INFORM THEIR MANAGER IF INVITED TO INTERVIEW FOR THE POSITION.
Job ID: 1032405
Location: India
Last Date : 14th June, 2016
Location: India
Last Date : 14th June, 2016
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