Should have knowledge of Water System, HVAC, Tabletting machinery and instruments.
Will be responsible for the up-keep of the production facility and the equipment/instruments.
Should be well versed on all the quality systems.
Should have knowledge on the requirements of GMP for Solid Dosage Form, especially for products which are exported to the Regulated Markets. (US, Europe, etc)
Ensure that all GMP Document entries are made contemporaneously & will be responsible for the data integrity in the department.
Should be able to handle deviations, change controls, CAPAs related to Production.
Should have skills to handle investigations and arrive at root causes.
Should be able to carry out Qualifications & Validations of the new equipment & existing equipment along with preparation of documents for the same.
Should be able to execute tech transfer of products.
Should be able to handle investigations relating to Market Complaints.
Will be responsible for the training of Workmen, Supervisors, Officers, Executives & Managers in the Production Department.
Support site QA & corporate QA in the assessment of monthly reviews.
Salary: INR 4,75,000 - 9,75,000 P.A.
Industry: Pharma / Biotech / Clinical Research
Employment Type: Permanent Job, Full Time