Intas Pharmaceuticals Ltd Walk-In 6th August 2022 for QA,IPQA (OSD & Injectable)/Process & Cleaning Validation

 Intas Pharmaceuticals Ltd Walk In Interview 2022 B.Pharm/M.Pharm for QA,IPQA: (OSD & Injectable)/Process & Cleaning Validation At Ahmedabad. Intas Pharmaceuticals Ltd Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.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.

Vacancy details:

  • Post Name: QA,IPQA: (OSD & Injectable)/Process & Cleaning Validation
  • Qualification: B.Pharm/M.Pharm   

Job Description: Intas Pharmaceuticals Ltd Hiring For QA,IPQA: (OSD & Injectable)/Process & Cleaning Validation !

Important Details :

  • Location: Ahmedabad
  • Date:6th August 2022
  • Time: 9.30 AM – 1.00 PM
  • Venue:-Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210
  • Selection Process: The selection will be on the basis of Interview.

Job description.

Roles and Responsibilities

In-process activities, line clearance

Preparation & Review of master BMR & BPR.

  • Process & Cleaning Validation (OSD & Injectable)

To prepare, review and execute Process Validation Protocols & Reports for Solid Oral and Injectable formulations.

To prepare, review and execute Packaging Validation protocols & reports for Solid Oral and Injectable formulations.

Preparation, Execution and Compilation of Process & Cleaning validation

  • Qualification: (Injectable)

To prepare qualification protocol of IQ, OQ, & PQ of equipment.

To execute validation exercise and compile data of qualification of equipment with respect to IQ, OQ & PQ.

Validation of utilities like; PSG (pure system), compressed air, water system etc.

To execute temperature mapping in the equipment / cold room/stability chambers & areas.

To schedule and execute re-qualification of equipment as and when applicable, close the CRF action plan after qualification activity

  • QMS CRF & Market Complaints

Should have knowledge on Change Control, Deviation, complaint Investigation, CAPA, Risk Assessment and trending of CRF, deviation and investigation.

Desired Candidate Profile

Candidate having relevant experience in QA i.e. IPQA, Validation-(PV & CV), Qualification, QMS and Doc Cell

Minimum 1 year of experience is required & Fresher need not to apply

Candidates having relevant experience in pharmaceuticals industry should only apply

Ready to work in rotational shifts

About Company:

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world. It has been growing at about 25.5% CAGR over the last 5 years and crossed the $1.9 billion mark in the past financial year. The company has set up a network of subsidiaries, under the name Accord Healthcare in EU, US, Canada, SA, Australia, APAC as well as CIS & MENA regions. Intas is present in 85+ countries, with more than 69% of its revenue coming from global business.

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