Home Head/VP/CEO/President/GM GM - Quality Control | Intas Pharmaceuticals | Ahmedabad

GM – Quality Control | Intas Pharmaceuticals | Ahmedabad

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Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon.

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With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors. A variety of initiatives in Research and Development, patents and ANDA filing, NDDS, quality manufacturing support, along with approvals by regulatory authorities of many countries has made Intas a global healthcare provider. Pioneering efforts in providing medications for both chronic and acute medical conditions have truly led Intas to live up to its corporate line Expressions for a Healthy Life.

Position: GM Quality Control

Location: Ahmedabad, Gujarat, India

Job Description:

  • To ensure accurate, reliable, efficient, and timely testing of Finished product, In-process /Process Validation sample, Raw materials, and release / reject of the same.
  • To establish measures for product quality and provide data to management.
  • To provide a safe work environment in Quality Control and support EHS policy of the company
  • To ensure accurate document preparation/review procedures being carried out related to Finished product, In-process, Process Validation products, Raw materials as per the regulatory norms.
  • To ensure Current Good Laboratory Compliance and ensure all SOPs related to Quality Control Laboratory are prepared and reviewed/implemented properly.
  • To ensure the proper functioning of all instruments. To reduce instrument idle time and breakdown.

  • To ensure the timely qualification of instruments, preventive maintenance, Annual Maintenance / Calibration of Instruments (INHOUSE or Outside)
  • To ensure the inventory of various Columns, Consumables & Spares, Reference/Working /Impurity Standards
  • To investigate/review OOS, OOT, and Incidents and to take remedial measures wherever required.
  • To ensure a review of validation/qualification protocol and reports.
  • To ensure Training to laboratory staff with respect to analytical technique/Quality control procedures/regulatory requirements.
  • Any other work allotted by the superior.
  • To ensure the Release of Raw material in SAP. Review and signing of Certificate Of Analysis generated in Quality Control.
  • To represent the department in case of regulatory audits, vendor audits, etc.

Qualification: B.Sc/B.Pharma, MS/M.Sc/M.Pharma

Experience: 20-25 Years

Salary: Negotiable

Contact Details:

careers@intaspharma.com, ashishn_mehta@intaspharma.com

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