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qms manager

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  • chandigarh, chandigarh
  • posted 14 october 2025
this job offer closes 13 december 2025

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this job offer closes 13 december 2025

summary

  • chandigarh, chandigarh
  • a client of randstad india
  • permanent
posted 14 october 2025
  • reference number
    JPC - 107172

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randstad professional

randstad professional

we bring diverse and pre qualified professional talent and businesses together to connect the right people with the right roles. by building specialized teams, we help individuals flourish in their careers and businesses succeed.

job details
Dear JobSeekers, We have an opportunity for PV Auditing & QMS Manager with a leading CRO. Mode of Working: HybridLocation: ChandigarhExperience: 5-6 years in PV and/or GCP and Quality Assurance Job description 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, specially planning for audits using 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 jhelam.s@randstad.in  

experience

7 ...
Dear JobSeekers, We have an opportunity for PV Auditing & QMS Manager with a leading CRO. Mode of Working: HybridLocation: ChandigarhExperience: 5-6 years in PV and/or GCP and Quality Assurance Job description 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, specially planning for audits using 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 jhelam.s@randstad.in  

experience

7