Job Description

For over 50 years, SCIEX has been developing groundbreaking technologies and solutions in mass spectrometry and capillary electrophoresis. Our products enable our customers to quickly respond to environmental hazards, better understand biomarkers relevant to disease, improve patient care in the clinic, bring relevant drugs to market faster and keep food healthier and safer. At SCIEX, you\'ll find a rewarding role that amplifies your impact on the world and helps you realize life\'s potential. SCIEX is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Interested in putting your computer, software, and network skills to work helping our customers achieve compliance in their efforts to develop and manufacture pharmaceutical therapies The Software Validation Specialist provides technical expertise to assist customers in validating mass spectrometry systems for 21 CFR Part 11 compliance in GxP regulated laboratory environments. The Software Validation Specialist is responsible for working with customers to modify and execute validation scripts addressing the customer\'s requirements, configurations, workflows, data management processes, etc. This position is part of the Global Compliance and Professional Services team and will be located remotely in India. Location - Mumbai In this role, you will have the opportunity to: Deliver consultative software validation services to SCIEX customers Work closely with customer IT, QA, and laboratory personnel throughout the entire validation process, (planning, documentation development, review, approval, and execution) Manage validation project scope and timelines to both SCIEX and customer expectations Coordinate engagements with local Field Service team Provide customer training as needed for adapting customer workflows to validation strategy. The essential requirements of the job include: Bachelor\'s degree (B.S./B.A.) in life sciences, informatics, information technology, computer science, or equivalent professional experience 2+ years of demonstrated experience in validating Life Sciences Systems in GLP and/or GMP laboratories Demonstrated expertise in global regulatory frameworks and requirements as they apply to LC-MS systems and software It would be a plus if you also possess previous experience in: Experience in validating Life Sciences Systems in GLP and/or GMP laboratories Experience in use and administration of SCIEX software When you join us, you\'ll also be joining Danaher\'s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you\'ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful tools and the stability of a tested organization. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. If you\'ve ever wondered what\'s within you, there\'s no better time to find out.

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