Job title: Quality Strategy Lead Development (all genders)
Company: Merck Group
Job description: A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the wo
A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Your Role: The RDQ Quality Strategy Lead Development will be mainly responsible for managing clinical programs day to day activities from quality assurance perspective and delivering the full range of quality related activities in support of the program. The incumbent works closely with the project/program teams and is accountable for stablising the quality assurance strategy in support of the program and to utilize/develop RDQ tools to deliver the strategy. You will lead multidisciplinary or cross-functional work/project teams and actively share knowledge with others across multiple disciplines and across lines through existing knowledge sharing processes and systems. Strong technical expertise is a must as you will additionally lead complex projects and coach and mentor other colleagues in our field of Research & Development (R&D). Who you are: Minimum 10 years QA experience or relevant experience in pharmaceutical and/ or biotech industry, in particular clinical quality management, biomedical science, clinical development, or regular compliance with a minimum of 5 years in Clinical / Medical QA. Comprehensive demonstrated working knowledge of principles and concepts of Quality Assurance and wide range of auditing skills covering a broad range of areas and/or specialized auditing skills in multiple disciplines – including those related to Risk Based Quality Assurance and Root Cause Analysis. In depth knowledge of drug development process and international GCP regulations and pharmacovigilance guidelines Comprehensive working knowledge in the areas of oncology, biotherapeutics, and emerging markets. Broad working knowledge of other GxP disciplines like GLP, GCLP, GMP or GPvP Proven ability to function autonomously at a senior level in a matrix model and in a team environment. This position can be based flexibly within Europe, based on the preference of the candidate. What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life! Curious Apply and find more information at
Expected salary:
Location: Bangalore, Karnataka
Job date: Sat, 21 May 2022 22:41:53 GMT
Apply for the job now!
