Opportunity to work as Pharmacovigilance Deputy Manager at Piramal Pharma- Apply before 20th April 2025

About Piramal Pharma

Piramal Pharma Solutions is a leading Contract Development and Manufacturing Organization (CDMO) providing comprehensive end-to-end development and manufacturing solutions across the drug life cycle. With a globally integrated network of facilities in North America, Europe, and Asia, we offer a wide range of services, including drug discovery, process & pharmaceutical development, clinical trial supplies, and commercial API & finished dosage form manufacturing.

Position: Deputy Manager – Pharmacovigilance

Location: Kurla, Mumbai
Experience: 3-5 years
Qualification: Bachelor’s/Master’s Degree in Pharmacy
Industry: Pharma / Healthcare / Clinical Research
Functional Area: Pharmacovigilance
Application Deadline: 20th April 2025

Roles and Responsibilities

• Prepare and review aggregate safety reports (PADERs, PSURs) for human and veterinary products as per regulatory requirements.

• Draft Risk Management Plans (RMPs).

• Perform end-to-end case management, including case receipt, database entry, peer review, and submission to regulatory authorities within specified timelines.

• Conduct literature monitoring for company molecules.

• Coordinate with internal and external stakeholders to ensure compliance with Pharmacovigilance responsibilities.

• Ensure adherence to company SOPs, procedures, and local privacy regulations.

• Assist in Pharmacovigilance inspections by regulatory agencies such as FDA, MHRA, and EMA.

Key Competencies

• Strong knowledge of aggregate safety report authoring, including PADERs and PBRERs.

• Excellent written and verbal communication skills.

• Ability to manage multiple projects and meet strict deadlines.

• Strong interpersonal and collaboration skills.

• Proficiency in Microsoft Word, Excel, and PowerPoint.

• Ability to work independently and as part of a team.

Candidate Profile

• Bachelor’s or Master’s degree in Pharmacy.

• 3-5 years of experience in safety report preparation, literature screening, and authoring of aggregate safety reports.

Why Join Us?

• Be part of a globally recognized CDMO offering cutting-edge pharmaceutical solutions.

• Work in a dynamic and collaborative environment.

• Gain exposure to international regulatory standards and global markets.

If you are passionate about Pharmacovigilance and looking for a challenging opportunity, apply now!