Pharmacovigilence Quality Assurance Lead

Location
Industry
Contract Type
Permanent
Published
Contact
Nandini Tyagi
Reference
29-2-15414
Academic title
Job description

Job description for the position of Pharmacovigilance (PV)/GCP QA Lead

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

  • Handling client audits and regulatory inspections
  • 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 internal and vendor 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

Note: This is only an indicative list, not an exhaustive list of responsibilities. Additional

activities may need to be performed.

Qualifications and skills:

  • Degree in any of the Life Sciences disciplines (Pharmacy, Microbiology, Biochemistry,

Biotechnology etc.)

  • Experience of ~10 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)

Job Description

Page 1

  • Auditing experience, specially planning for internal and vendor audits using risk-based approach
  • Experience in handling client/partner audits, and regulatory inspections
  • 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
Requirements

Experience of ~10 years in Pharmacovigilence and/or GCP and Quality Assurance

Other notes
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