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Sun Pharma Hiring Freshers & Experienced For Pharmacovigilance & BioAnalytical Roles

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Sun Pharma is the world’s fourth-largest specialty generic pharmaceutical company and India’s top pharmaceutical company. With a global presence in over 100 countries, Sun Pharma is committed to delivering high-quality, affordable medicines. The company focuses on innovation, R&D, and maintaining the highest compliance standards in pharmacovigilance and bioanalytical research.


1. Job Opening: Executive โ€“ R&D Quality (GPvP-QA) โ€“ Pharmacovigilance Auditor

Job Location: Gurgaon

Key Responsibilities:

  • Develop and execute aย global Pharmacovigilance (PV) auditing programย for CROs, vendors, affiliates, and partners.
  • Conduct audits (as lead/co-auditor) to ensure compliance withย GVP modules, ICH-GCP, and regulatory guidelines.
  • Reviewย Pharmacovigilance SOPsย for compliance with global policies.
  • Maintainย CAPA trackerย and ensure timely closure of corrective actions.
  • Assist inย risk assessment of business partnersย and vendor qualification.
  • Reviewย Periodic Safety Update Reports (PSURs) and Pharmacovigilance System Master Files (PSMFs).
  • Updateย audit master schedulesย and manage theย Internal Audit Observation Database (IAOD).

Desired Candidate Profile:

  • M.Pharmย withย 2-3 years of experience in PV-QA or Pharmacovigilance operations.
  • Strong knowledge ofย GVP modules, ICH-GCP, and global PV regulations.
  • Excellentย communication and auditing skills.

Keywords: Pharmacovigilance Quality Assurance, PV Auditing, GVP, R&D Quality, RQA, CAPA Management


2. Job Opening: Executive – Innovative Projects (Bioanalytical Operations)

Job Location: Tandalja (R&D)

Key Responsibilities:

  • Performย bioanalytical sample processingย for drug and metabolite analysis.
  • Ensure compliance withย USFDA, ANVISA, and ICH guidelines.
  • Operate and maintainย LC-MS/MS instruments.
  • Develop and validateย bioanalytical methodsย for biological samples.
  • Maintainย GLP complianceย in documentation and lab safety.
  • Prepareย SOPs, protocols, and study reports.
  • Conductย literature surveysย for method development and validation.

Desired Candidate Profile:

  • 0-1 year of experienceย inย bioanalytical research.
  • Strong knowledge ofย LC-MS/MS, regulatory guidelines (USFDA, ICH).
  • Understanding ofย GLP principlesย and lab safety.

Keywords: Bioanalytical Research, LC-MS/MS, Method Validation, GLP, USFDA Compliance


How to Apply?

Interested candidates can apply through Sun Pharmaโ€™s careers portal or send their updated resumes to the HR department.

๐Ÿ“Œย For Gurgaon (PV-QA) Role:ย Apply Here
๐Ÿ“Œย For Tandalja (Bioanalytical) Role:ย Apply Here

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