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Online Resumes with "IND CTA"
Seeking research position where ten years of pre-clinical pharmaceutical/biotechnology experience will serve to benefit this function in the equivalent industry.
My ideal position will be one that matches my skill set thus far as I truly enjoy the work that I perform. Ten years of experience and a diverse background in the pharmaceutical and biotechnology industries have given me the knowledge and skills to be an active contributor in this field. I have a proven record of accomplishment in CRO project management, coordination of toxicology studies, QC and auditing for IND, CTA and...
Tags for this Online Resume: in vivo, preclinical, toxicology, animal
Senior Technical Editor, Electronic Document Coordinator/Specialist
Regulatory Affairs Associate
Fulltime opportunity in Regulatory Affairs Function
Tags for this Online Resume: Regulatory Submission, ECTD, PDF Editor, SPL, Regulatory Compliance, Regulatory Compliance/FDA/EMA (EU), Clinical Trials, NDA/ANDA/IND/CTA, Medical Devices
Biochemist
Tags for this Online Resume: Regulatory Affairs , FDA EMA, NDA MAA, Compliance , Clinical - CMC, Leadership, Experienced IND CTA, Proficient- Pragmatic , Innovation
Global Regulatory Affairs - 14 Years of Experience- New Delhi India 110021
Seeking assignments as a Global Regulatory Affairs Professional - NCEs, GENERICS- Pharma, Biotech products, Botanicals & Medical Devices in Global Regions and/or Quality & Compliance professional across the Pharma & Medical Devices Industry. Overall Profile * With overall 15+ years industrial experience, with 14+ years in the field of Global Regulatory Affairs, Compilation & Submissions of Technical Packages for IND/CTA, ND...
Ideal Companies: BBraun Medical Pvt Ltd, New Delhi, India, Glenmark Pharmaceuticals Ltd., Mumbai, India, Panacea Biotec Ltd., New Delhi, India
Tags for this Online Resume: Regulatory Affairs, Management, Medical Devices, Pharmaceutical Industry, IND/CTA, Formulations & APIs, Regulatory Audits & Compliances, NCEs/NMEs/Generics, CT, Regulatory Consultancy, Regulatory Due Diligence & Gap Assessment
Chemist - 20 Years of Experience - Near 02467
PROFESSIONAL SUMMARY * A proven leader with a track record of accomplishments with more than fifteen years pharmaceutical industry experience in leading analytical development activities for small molecule drug development * Hands-on experience in analytical project management in drug development and regulatory submissions hands- on experience in analytical method development/validation/transfer in GMP environments expertis...
Tags for this Online Resume: High Performance Liquid Chromatography (HPLC), Quantify, Analytical Chemistry, Chemistry, Research, Research and Development, Regulatory Affairs, Applications, CMOS, Development Activities
