PV Specialist - EUG Operations

Dr. Reddy's Laboratories; Hyderabad; On-site; INR 1,800,000 - 2,400,000; Full time

Job summary

Dr. Reddy’s Laboratories in Hyderabad seeks an experienced Pharmacovigilance professional to support EU/UK PV activities, maintain RMPs, and coordinate PSURs and variations under supervision.

The role requires B.Pharm/M.Pharm with 6–12 years in PV, strong knowledge of EU/UK regulations, and proficiency with MS Word/Excel/PowerPoint. On‑premise, cross‑functional collaboration with global PV teams.

Qualifications

• Education: B.Pharm/ M.Pharm with 8+ years of experience.
• Good working knowledge of EU and UK PV regulations.
• Performs timely coordination of safety information dissemination.
• Excellent teamwork and interpersonal skills; time management and organizational skills.
• Good knowledge of computer applications and software, including MS Word, Excel, PowerPoint etc.

Responsibilities

• Under supervision of EU/UK QPPV, manage EU RMPs and UK RMPs and trackers.
• Handle PSUR data collection and QC; manage RMP variations and tracking with RA.
• Eudravigance data handling and signal detection; track PSUSAs and actions for next PSUR.
• Deviation & CAPA support; post-authorisation updates of RMPs and related variations.
• Interact with EU/UK PV teams and vendors for PV activities; ensure activity tracking through spreadsheets.

Skills

Teamwork

Interpersonal skills

Time management

Organizational skills

MS Word

MS Excel

PowerPoint

Education

B.Pharm/M.Pharm

Tools

MS Word

MS Excel

PowerPoint

Job description

Company Description

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.

We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).

‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency

Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.

Job Description

This role is responsible to support the EUG PV activities while performing below mentioned activities.

Responsibilities

• Under the supervision of the EU/UK QPPV, managing the EU RMP and UK RMPs and their trackers.
• SmPC updates and Safety variation initiation, tracking.
• Handling of RMP queries, Cmdh intimation of risks.
• PSUR data collection and QC.
• ACOs data collection and QC.
• Tracking and Documentation: ensure all activities are tracked through the maintenance of activity tracking spreadsheets.
• Eudravigilance database handling and Signal detection.
• Regulatory Intelligence: Monitor PSUSAs and track the activities to be addressed in next PSUR.
• Post authorisation update of RMPs - initiation and its related variations tracking with RA.
• Deviation & CAPA Support
• Prior Audit and inspection experience.
• Any other activities assigned by reporting Manager.

Relationship Management

• Working with EU or UK PV team, Global PV team.
• Interactions with vendor’s/service providers for PV activities

Process Improvement / Standardization

• Participate in process improvement initiatives under supervision of UK/EU QPPV.

Qualifications

Education: B.Pharm/ M.Pharm with 8+ years of experience.

• Good working knowledge of EU and UK PV regulations
• Performs timely coordination of safety information dissemination
• Excellent teamwork and interpersonal skills Excellent time management and organizational skills.
• Good knowledge of computer applications and software, including MS Word, Excel, PowerPoint etc.

Additional Information

This role is a part of Pharmacovigiliance for EUG & will be based in Hyderabad location.

• Job Family: Medical Affairs & Pharmacovigilance
• Sub Job Family: Pharmacovigilance
• Preferred type of working: On-Premise
• Years of Experience: 6 - 12
• Business unit: EUG