.Company DescriptionDr.
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 and to build the future.'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.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.Job DescriptionWe are looking for Immediate joinees for this role.Activities:Maintenance of master product list for Europe and its reference product list.SOPs/Wis support.Drafting deviations and CAPAs, effectiveness check.Support QPPV in implementation of new PV activities as per new guidelines by arranging trainings and calls with relevant stakeholders.PSUR submission support.Latest MA status, SmPC and PIL sharing with call centers and other EU vendors to perform routine activities.Product Batch number confirmation.EU PV activities adhoc support to interact with other departments for cross functional issues and alignment.Eudravigilance access management.Desired Skills:Prior Pharmacovigilance experience with PV activities and team interactions.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:B.Pharm/M.Pharm with 4-5 years of experience.Desired Skills & Competencies:Excellent teamwork and interpersonal skills.Excellent time management and organizational skills.Good knowledge of computer applications and software, including MS Word, Excel, PowerPoint etc.Benefits Offered:At Dr. Reddy's we actively help to catalyse your career growth and professional development through personalised learning programs