Gcp/Pv Auditor Specialist

Job Summary: We are seeking a highly motivated and detail-oriented Gcp/Pv Auditor - Compliance Specialist to join our team at Novartis Farmacéutica, S.A. As a Gcp/Pv Auditor - Compliance Specialist, you will be responsible for planning, leading, conducting, documenting, reporting, and following up on GCP/PV audits according to Novartis procedures and...

Job SummaryIn this role, you will lead and support independent GCP/PV audits, ensuring compliance with Novartis Quality Systems and Standards, Good Clinical Practice (GCP)/Good Pharmacovigilance Practice (GPvP), and current GCP/PV regulations. You will provide quality guidance and assist in identifying and implementing quality assurance training needs for...

About the RoleIn this role, you will lead, support, and report independent GCP/PV audits and approve follow-up corrective and preventive activities according to Novartis Quality Systems and Standards, Good Clinical Practice (GCP)/Good Pharmacovigilance Practice (GPvP), and current GCP/PV regulations.You will provide GCP/PV-related quality guidance and assist...

We are seeking a highly skilled Gcp/Pv Senior Auditor to join our team at Novartis. As a key member of our Global Auditing team, you will be responsible for managing cost-effective GxP Compliance and/or Audit activities, operations, and systems to ensure compliance with the Novartis Quality Manual and Policies and all relevant GxP, legal, and regulatory...

This role with Novartis focuses on leading and supporting GCP/PV audits to ensure compliance with quality systems and standards. You will provide guidance on GCP/PV related quality issues and assist in identifying and implementing quality assurance training needs.Key Responsibilities:Plan, lead, conduct, document, report, and follow-up of GCP/PV audits...

About the JobWe are seeking a highly skilled Global Quality Assurance Expert to join our team as a GCP/PV Auditor. In this role, you will lead and support independent audits, ensuring compliance with Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GPvP) regulations.

About the RoleIn this role, you will lead and support independent GCP/PV audits, ensuring compliance with Novartis Quality Systems and Standards, Good Clinical Practice (GCP)/Good Pharmacovigilance Practice (GPvP), and current GCP/PV regulations.You will provide GCP/PV related quality guidance and assist in identifying and implementing quality assurance...

Discover a rewarding opportunity to shape the future of healthcare with Novartis as a Senior Compliance Auditor. About the RoleThis position comes with a flexible location and we are ready to hire this role in the city of preference (within Spain) of the successful candidate.In this exciting role, you will lead and support independent GCP/PV audits and...

About the Role:The position of GCP/PV Auditor is available at ES06 (FCRS = ES006) Novartis Farmacéutica, S.A. The successful candidate will be responsible for conducting audits and assessments to ensure compliance with regulatory requirements.

Job SummaryWe are seeking a highly skilled Senior Auditor to join our team at Novartis. As a Senior Auditor, you will be responsible for managing 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...

Company Overview: Es06 (Fcrs = Es006) Novartis Farmacéutica, S.A. is a renowned pharmaceutical company committed to reimagining medicine and improving people's lives.Job Title: Global Quality Assurance AuditorEstimated Salary: $85,000 - $110,000 per annum, depending on location and experience.Job Description:In this exciting role as a Global Quality...

Job Title: GCP AuditorLocation: Global Innovative Clinical Dept.Functions:Plan, lead, execute, report on, follow up and/or oversee audits held by both the GSMQA and by external auditors.Guarantee the execution of and compliance with any Quality Assurance Program established for the clinical studies.Host and coordinate any external audits/inspections...

About the RoleAt Innovative Medicines, we are seeking a highly skilled Quality Compliance and Risk Manager (GCP/PV) to join our team. As a key member of our organization, you will play a critical role in ensuring the highest quality standards in our research and development processes.Key ResponsibilitiesSupport the development and implementation of risk...

Job Summary:We are seeking a highly motivated and experienced individual to join our team as a GCP/PV Auditor. The successful candidate will have a thorough understanding of GCP, GPvP, and GxP regulations and guidelines.Key Responsibilities:Plan, lead, conduct, document, report, and follow-up of GCP/PV audits according to the requirements specified in the...

About QualifyzeQualifyze is a leading company in supply chain compliance management in the Life Sciences industry, trusted by over 1,200 pharmaceutical and healthcare companies globally. Our digital suite of solutions connects manufacturers, suppliers, and a global network of more than 250 auditors and quality experts. With a track record of over 3,000...

About QualifyzeQualifyze is a leading company in supply chain compliance management in the Life Sciences industry, trusted by over 1,200 pharmaceutical and healthcare companies globally.Our digital suite of solutions connects manufacturers, suppliers, and a global network of more than 250 auditors and quality experts.With a track record of over 3,000 audits...

About the RoleWe are seeking a highly skilled Senior Quality Assurance Specialist to join our team at Qualifyze, a leading company in supply chain compliance management in the Life Sciences industry. This role is critical in ensuring that our auditing processes, particularly in Pharmacovigilance (PV), align with applicable GxP standards and...

About the RoleWe are seeking a highly skilled Quality Assurance Specialist to join our team at Qualifyze. As a key member of our Quality Team, you will play a crucial role in ensuring that our auditing processes meet the highest quality standards, particularly in the area of Pharmacovigilance (PV).Key ResponsibilitiesEnsure that our services meet all...

About QualifyzeWe are a leading company in supply chain compliance management in the Life Sciences industry, trusted by over 1,200 pharmaceutical and healthcare companies globally.Our digital suite of solutions connects manufacturers, suppliers, and a global network of more than 250 auditors and quality experts.With a track record of over 3,000 audits across...

About the RoleThe Senior PV Associate Analytics role at Galderma offers a competitive compensation package with an estimated salary of $120,000 annually.