Apcer Life Sciences Ahmedabad Vacancy | Pharmacovigilance Jobs

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About Apcer Life Sciences:

Apcer Life Sciences is a company that provides services to pharmaceutical and biotech companies around the world. They focus on patient safety and ensuring that medications are effective and safe. Here’s a breakdown of their key areas:

  • Drug Safety/Pharmacovigilance: They help manage the risks associated with medications throughout their lifecycle. This includes collecting and reporting adverse events.
  • Medical Information and Writing: Apcer Life Sciences can create medical documents and answer questions from healthcare professionals about medications.
  • Regulatory Services: They help companies navigate the regulations required to get drugs approved and marketed around the world.
  • Quality Assurance and Risk Management: Apcer Life Sciences helps ensure that all their services are delivered according to high quality standards and that potential risks are identified and managed.

They seem to have a global presence with offices in Ahmedabad, Delhi and potentially other locations. Their website lists their commitment to patient safety as a core value.

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About Apcer Life Sciences Ahmedabad Vacancy:

Hi Folks!

We are hiring for a Manager – Quality & Compliance (PV QA) based out at the Ahmedabad location.
Interested candidates with relevant experience can share their CVs on suraj.kumar@apcerls.com

Job Role:
1. Participate in the risk assessments and preparation of a risk-based audit plan for auditing internal processes, vendors and customers.
2. Prepare and/or review audit plan, audit agenda, document request log, audit report and audit responses as assigned.
3. Conduct internal audits within APCER according to the Audit Plan.
4. Conduct external audits including the audit of vendors, clients and/or client’s business partners and service providers.
5. Participate and support in external/client audits and regulatory inspections to be hosted by APCER.
6. CAPA management (Tracking, review and management) of audit and inspection CAPAs. Follow-up as required for compliance to CAPA timelines.
Providing PSMF data/update for Annex G requests.
7. QA and Department specific report Preparation.


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