Pharmacovigilance

Hyrix; Mumbai; Presencial; INR 550.000 - 900.000; Jornada completa

Descripción de la vacante

Hyrix is seeking experienced professionals in Pharmacovigilance and Medical Device Complaint Management for a Mumbai-based role working from office in US night shifts.

Positions are SPE/ SME levels with 1–5 years of experience, offering compensation between 5.5 LPA and 9 LPA per year. The role emphasizes process discipline, quality compliance and cross-functional collaboration in a fast-paced environment.

Formación

• Strong organizational, coordination and stakeholder management skills.
• Excellent verbal and written communication abilities.
• Analytical mindset with focus on process and operational excellence.
• Detail-oriented with ability to follow SOPs and policies.
• Knowledge of Clinical Research & Pharmacovigilance processes.

Responsabilidades

• Review complaint cases for accuracy and compliance.
• Ensure adherence to SOPs, work instructions and policies.
• Track and communicate compliance metrics.
• Handle data review for special scenarios and escalations.
• Coordinate with internal and external stakeholders for issue resolution.
• Provide training and support to team members.
• Support commercial systems aligned with strategic initiatives.

Conocimientos

Organizational skills

Verbal communication

Written communication

Analytical mindset

Attention to detail

Stakeholder management

Pharmacovigilance

Medical Device

Descripción del empleo

Hiring Alert | SPE / SME – Pharmacovigilance & Medical Device Complaint Management

We are looking for experienced professionals in Pharmacovigilance and Medical Device Complaint Management for a leading organization.

Pharmacovigilance & Medical Device Complaint Management

• Location: Mumbai
• Work Mode: Work from Office
• Shift: Night Shift (US Shift)
• Experience: 1 to 5 Years
• Level: SPE-5.5Lpa / SME-9Lpa
• Candidates with Pharmacovigilance experience can also be considered if Medical Device Complaint Management experience is limited.

Essential Skills

• Strong organizational and team coordination skills
• Good verbal & written communication
• Analytical mindset with operational excellence approach
• Process-driven with strong attention to detail
• Team player with stakeholder management skills
• Knowledge of Clinical Research & Pharmacovigilance process

Key Responsibilities

• Review complaint cases for accuracy, consistency & compliance
• Ensure adherence to SOPs, work instructions & policies
• Track and communicate compliance metrics
• Handle case data review for special scenarios
• Coordinate with internal & external stakeholders for issue resolution
• Escalate critical issues/problems to management
• Provide training and support to team members
• Support commercial systems aligned with strategic initiatives

Preferred Candidate Profile

• Experience in Pharmacovigilance / Medical Device Complaint Management
• Strong quality & compliance understanding
• Comfortable working in US Night Shift
• Ability to work in fast-paced environments