
Gcp/pv Auditor
3 days ago
**Summary**:
- Manage cost effective GxP Compliance and/or Audit activities, operations and systems to ensure compliance of business areas with the Novartis Quality Manual and Policies and all relevant GxP, legal and regulatory requirements, and through internal audits, KPIs (Key Performance Indicators) and KQIs (Key Quality Indicators) -Performs preparation and management of external and corporate audits and Health Authority inspections.
**About the Role**:
GCP/PV Senior Auditor
Location - Mumbai #LI Hybrid
About the Role:
Lead, support, and report independent GCP/PV audits according to the Novartis Quality Systems and the current GCP/PV regulations to assess compliance with applicable regulations, standards, and guidance documents. Review and approve corrective action plans in support of the audit observations. Ensure alignment with the company's strategic direction and assist in driving the implementation of the applicable actions. Provide consultation to NVS business units through risk-based assessments. Act as SME for assigned areas of responsibility.
Key Responsibilities:
- Support the strategic development of an effective global risk-based audit strategy
- Provide technical guidance and training on audit activities. Maintain current knowledge of regulations, standards, and guidance documents.
- Ensure appropriate escalation to responsible management in case of critical audit findings and support immediate follow-up measures according to the Novartis requirements on Management Escalations and other relevant procedures. Ensure adequate definition and recording of mitigation plans when applicable.
- Assess the adequacy of responses (CAPA plans) to audit findings in cooperation with Follow-up Responsible Person (FURP) and Quality Responsible Person (QARP)
Essential Requirements:
- 10+ years of proven experience in GCP/GPvP/clinical/industry/health authority experience or equivalent.
- 5+ years of GCP/PV auditing experience preferred and willingness to travel up to 60% of the time.
- Ability to lead and objectively evaluate compliance issues. Ability to address a variety of tasks within the same timeframe while maintaining oversight; maintain a moderate degree of independence with respect to decision-making and problem-solving
- Experience with Health Authority inspections and interactions preferred. Good quality and compliance leadership and facilitation skills.
- Excellent verbal and written communication, organizational, and interpersonal skills. Excellent computer skills including Excel, MS Office etc.
Desirable Requirements:
- Graduate in natural/biological sciences or equivalent, or an equivalent mix of education and experience
Division
Operations
Business Unit
Pharmaceuticals
Location
India
Site
Mumbai (Head Office)
Company / Legal Entity
IN10 (FCRS = IN010) Novartis Healthcare Private Limited
Functional Area
Quality
Job Type
Full time
Employment Type
Regular
Shift Work
No
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
-
Senior GCP/PV Auditor
1 week ago
Mumbai, Maharashtra, India Sandoz Full timeJob Description- Support the strategic development of an effective global risk-based audit strategy and program; collect, collate, and incorporate input into audit strategy and plan.- Lead, plan, conduct, document, and follow-up of global quality regulatory compliance audits and assessments of GCP/GPvP according to the requirements specified in the...
-
Global Audit Strategist
7 days ago
Mumbai, Maharashtra, India beBeeAudit Full time ₹ 17,50,000 - ₹ 21,80,000Job OpportunityThe Senior GCP/PV Auditor will play a key role in developing and implementing a global risk-based audit strategy.Key ResponsibilitiesLead the planning, execution, documentation, and follow-up of global quality regulatory compliance audits and assessments of GCP/GPvP.Provide expert guidance and training to other auditors on audit-related...
-
Global Compliance Assurance Leader
1 week ago
Mumbai, Maharashtra, India beBeeAuditor Full timeSenior GCP/PV Auditor Job DescriptionThis is a senior-level position responsible for leading and conducting global quality regulatory compliance audits and assessments of GCP/GPvP.The ideal candidate will have extensive knowledge of applicable GCP, PV, and GxP regulations, guidelines, policies, and procedures. They will also have excellent leadership and...
-
Senior Compliance Auditor
1 week ago
Mumbai, Maharashtra, India beBeeAuditor Full timeJob SummaryThis is a critical leadership role that requires exceptional experience in GCP/PV auditing, regulatory compliance, and quality management. The ideal candidate will have a strong track record of leading global audits, conducting thorough risk assessments, and providing technical guidance to team members.About the RoleLead the development of a...
-
Mumbai, Maharashtra, India beBeeAudit Full time ₹ 1,08,00,000 - ₹ 1,44,00,000As a senior quality assurance professional, you will play a key role in shaping the company's audit strategy and ensuring compliance with global regulatory standards. Your expertise will be invaluable in conducting audits, providing technical guidance, and mentoring junior auditors.Audit StrategyDevelop an effective risk-based audit strategy and program to...
-
Team Member
1 week ago
Mumbai, Maharashtra, India Sun Pharma Laboratories Ltd Full time**Title**:Team Member - Clinical Research**: - Date: Feb 17, 2025 - Location: Sun House - Corporate Office - Company: Sun Pharma Laboratories Ltd **YOUR TASKS AND RESPONSIBILITIES**: **CRO Managed Studies**: - Manage Contract Research Organization (CRO) for effective execution of interventional, non-interventional and epidemiological studies - Identify...
-
Clinical Research Associate
1 week ago
Mumbai, Maharashtra, India Sun Pharma Laboratories Ltd Full time**In-House Managed Studies** - Site feasibility, potential investigator identification and development of study budgets for each study - Finalization of investigators, sites and execution of CDA and study related contracts - Plan and conduct Investigator’s Meeting if needed - Preparation and submission of study documents for EC permission for respective...
-
Clinical Research Associate
1 week ago
Mumbai, Maharashtra, India Sun Pharma Laboratories Ltd Full time**Title**:Clinical Research Associate**: - Date: Sep 3, 2024- Location: Sun House - Corporate Office- Company: Sun Pharma Laboratories Ltd**In-House Managed Studies** - Site feasibility, potential investigator identification and development of study budgets for each study - Finalization of investigators, sites and execution of CDA and study related...
-
Officer - PV- Medical writer
2 days ago
Mumbai, Maharashtra, India Unichem Laboratories Full time US$ 90,000 - US$ 1,20,000 per yearRESPONSIBILITIESResponsible for management of scheduled and unscheduled aggregate reports including Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Addendum to Clinical Overviews (ACOs), United States Periodic Adverse Drug Experience Reports (PADERs), Risk Management Plan (RMP), Health Hazard Evaluation...
-
Hwc Pv
4 days ago
Mumbai, India WTW Full time**About WTW**: Our distinct, connected perspective across talent, assets and ideas unlocks potential for our clients. While many just look at mitigating the downside, we see how a unified approach to people and risk is a path to growth. Powered by market analytics and behavioral insight, our integrated teams reveal hidden value within the critical...