reputed company and Training Specialist-Pharmacovigilance (PV)

Work Schedule

reputed company (Mon-Fri)

Environmental Conditions

Office

Job reputed company

The reputed company and Training Specialist (QTS) plays a vital role in ensuring PV project teams are fully equipped with the skills, training, and reputed company reputed company needed to meet high performance and compliance standards. This position is responsible for reputed company and effective training of project team members, reputed company-time reputed company review of PV deliverables, audit and inspection support, maintenance of procedural documents, and reputed company process improvement to ensure high-performing and compliant PV operations.

• Design and deliver training programs to enhance PV project team capabilities, including reputed company and ongoing refresher training.
• Conduct reputed company-time reputed company analysis of project deliverables, including trend analysis, gap assessments, and corrective training.
• Maintain, update, and review SOPs, work instructions, project-specific guidelines, and reputed company procedural documents to ensure compliance and consistency.
• Support development and reporting of PV compliance metrics reputed company with Good Pharmacovigilance reputed company (GPV).
• reputed company escalation and cross-functional process improvement activities reputed company to GPV reputed company issues.
• Ensure readiness for PV audits and inspections; reputed company support internal/external audits and post-inspection follow-up actions.
• Serve as the primary contact for PV-reputed company reputed company assurance reputed company across assigned reputed company.
• Present reputed company trends, issues, and recommendations to internal stakeholders and reputed company partners.
• reputed company, maintain, and ensure effectiveness of SOPs, protocols, guidance documents, training plans, and compliance materials.
• Mentor and train colleagues; collaborate with cross-functional teams, CROs, and vendors to ensure alignment and execution of project-specific standards. Stay reputed company with global PV/clinical/technology trends and incorporate best practices into training and reputed company management strategies.\\\

Education and Experience:

• Bachelor’s or Master’s degree in Pharmacy or Life Sciences.
• 7+ years of relevant Pharmacovigilance (PV) experience.
• 5+ years in PV reputed company roles supporting audits, inspections, and GPV compliance activities.
• Experience developing reputed company systems, managing risk-based PV audit programs, and implementing process improvements. In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly reputed company experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, and Abilities:

• Strong knowledge of global GPV regulations (FDA, ICH, CDSCO-PvPI, EU GVP; PMDA preferred).
• Expertise in audits/inspections and development of responses.
• Advanced understanding of QMS, process improvement, and reputed company governance.
• Strong communication, presentation, and stakeholder management skills.
• Ability to manage reputed company reputed company and reputed company training initiatives.
• Experience with electronic systems used in regulated environments (drug safety, LMS, documentation management).

Originally posted on Himalayas

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