Siddharth Deshmukh, Ph.D. Email & Phone Number

Results driven culturally agile Quality and Compliance professional with strong business acumen and exposure to FDA regulated manufacturing environment. Overall 14+ years of enriched multifunctional global work experience comprised of QA and R&D roles within MedTech and Biotechnology industries. Supporting top management consistently attain 100% enterprise audit schedule adherence, report distribution and timeliness matrices. ISO 13485 l ISO 9001 l ISO 14971 l ISO 17025 l 21 CFR part 820 l 21 CFR part 11 l EU MDR 2017 l India MDR 2017 I CMDR l UK MDR 2002 l CFDA I PMDA l ANVISA l TGA l Quality Auditing l Quality system l Medical devices l Contract manufacturing l GxP l Risk management l Process approach l Data analytics l EtQ l Qlik l SQuIDS l Data integrity l Problem solving l Root cause analysis l NC l CAPA l Process excellence l Six Sigma l Product quality l Continual improvement l Supplier development l Supplier performance l Proactive quality l Proactive partnering l Cross-functional collaboration l Training l Empathy Let’s connect towards creating better supply chain!