Website Review & Compliance Report Specialist – Macleods Pharmaceutical Ltd | Mumbai

Jobs On The Way; Mumbai; On-site; INR 600,000 - 800,000; Full time

Job summary

Macleods Pharmaceutical Ltd in Andheri, Mumbai invites applications for the role of Website Review and Compliance Report Specialist. The position targets M.Pharm graduates with hands-on pharmacovigilance and global regulatory compliance experience seeking growth in a leading pharmaceutical company.

You will monitor regulatory websites worldwide, identify safety updates, draft SOPs, and maintain regulatory reports.

Qualifications

• 1–2 years of experience in pharmacovigilance or regulatory compliance.
• Strong knowledge of global regulations (GVP, MHRA, EU Regulations, USFDA).
• Excellent written and verbal communication skills.
• Strong interpersonal and teamwork abilities.

Responsibilities

• Daily review of regulatory and health authority websites across multiple countries.
• Identify safety-related updates and communicate them to stakeholders.
• Prepare and update SOPs, guidelines, and internal documentation.
• Coordinate with QPPV and LRPs teams.
• Draft and maintain compliance and regulatory reports.
• Organize and participate in meetings with QPPV and cross-functional teams.

Skills

Pharmacovigilance

Regulatory compliance

Global regulations

Communication skills

Education

M.Pharm

Job description

Macleods Pharmaceutical Ltd is inviting applications for the position of Website Review and Compliance Report Specialist at its Andheri, Mumbai location. This role is ideal for M.Pharm graduates with hands-on experience in pharmacovigilance and global regulatory compliance who are looking to grow with a leading pharmaceutical organization.

About the Role

As a Website Review and Compliance Report Specialist, you will play a critical role in monitoring global regulatory websites, identifying safety-related updates, and ensuring timely communication with internal and external stakeholders. You will also contribute to SOP management and compliance documentation aligned with global pharmacovigilance standards.

Key Responsibilities

• Daily review of regulatory and health authority websites across multiple countries
• Identify safety-related updates and communicate them to relevant stakeholders
• Prepare and update SOPs, guidelines, and internal documentation
• Coordinate with QPPV and LRP teams
• Draft and maintain compliance and regulatory reports
• Organize and participate in meetings with QPPV and cross-functional teams

Eligibility Criteria

• Experience: 1-2 years in Pharmacovigilance / Regulatory Compliance
• Strong knowledge of global regulations including:
  • GVP
  • MHRA
  • EU Regulations
  • USFDA
• Excellent written and verbal communication skills
• Strong interpersonal and teamwork abilities

Desired Skills

• Sound understanding of Pharmacovigilance processes:
  • PSMF
  • ICSR
  • PSUR
  • RMP
• Strong time management and organizational skills
• Ability to manage multiple compliance activities simultaneously