qms manager

1 day ago


Chandigarh, Chandigarh, India Randstad MENA Full time ₹ 12,00,000 - ₹ 36,00,000 per year
Job Description

Job details: This job offer closes 13 December 2025

Summary

Location: Chandigarh, Chandigarh
Company: A client of Randstad India
Employment Type: Permanent
Posted on: 14 October 2025
Reference Number: JPC

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Job Details

Dear Job Seekers,

We have an opportunity for PV Auditing & QMS Manager with a leading CRO.

Mode of Working: Hybrid
Location: Chandigarh
Experience: 5-6 years in PV and/or GCP and Quality Assurance

** for the position of Pharmacovigilance (PV) / GCP Auditing & QMS Manager:**

Performing QA activities (listed below) independently and/or in liaison with the Quality Head:

  • Management of quality issues/events/deviations and CAPAs
  • Performing RCAs and/or providing guidance to the staff in performing RCAs
  • Developing CAPA plans and/or providing guidance to the staff in developing and implementing CAPAs
  • Planning audits using a risk-based assessment and maintaining the audit planner in accordance with applicable GVP and GCP requirements
  • Preparing audit schedules and performing internal audits and audits of vendors
  • Maintaining/managing controlled documents such as SOPs, templates etc.
  • Liaising with Project Leads/Functional Heads for ensuring implementation of applicable KPIs/metrics
  • Reviewing the quality and compliance data of various projects; performing trend analyses and interpretation of analyses
  • Computer system validation activities
Qualifications and Skills:
  • Degree in any of the Life Sciences disciplines (Pharmacy, Microbiology, Biochemistry, Biotechnology etc.)
  • Experience of 5-6 years in PV and/or GCP and Quality Assurance
  • High level of proficiency in English, particularly written English
  • Auditing certification (e.g. ISO lead auditor/assessor certification)
  • Auditing experience, especially planning for audits using a risk-based approach
  • Experience in performing RCAs and development of CAPAs
  • Working knowledge of drug safety/GCP/regulatory requirements
  • Strong written and verbal communication skills
  • Detail oriented
  • Passion for delivering high quality work
  • Ability to manage multiple and varied tasks effectively
  • High level of flexibility and ability to prioritize work
  • Ability to perform under stringent timelines
  • Ability to work independently or as a team member
  • Excellent problem-solving skills and decision-making skills
  • Ability to understand, interpret, analyse and present data
  • Computer proficiency: proficiency in the use of MS Office suite (Word/Excel/ Power Point)
  • Ability and willingness to travel, as needed

Interested candidates can share CVs at



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