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Online Resumes with "Regulatory Affairs "
Quality Assurance&Regulatory Affairs Manager NYC
To manage or support company goals on time and improve continusly medical device regulatory and quality skills
VP, Medical and Clinical
Drug development, clinical study, medical affairs, safety, pharmacovigilance, regulatory affairs, translational medicine, modelling, simulation, preclinical research, IIS and ISS
RA
Ethical High energy professional with exceptional interpersonal, communication and leadership skills. Resourceful, creative, loyal
Ideal Companies: no preference
Medical Device Quality Consultant -helping firms build FDA compliant quality systems
Consulting projects to help medical device firms come into substantial compliance with FDA regulations.
Tags for this Online Resume: consultant , Quality , medical device, FDA compliance, regulatory affairs
Pharmaceutical Research / International Regulatory Affairs Scientist
To bring to a new team my extensive scientific background coupled with experience and knowledge of international regulatory affairs. I deeply enjoy working with a diverse group of people and functions, applying new information and strategies.
Manager Regulatory Affairs
I want to be employed in a position that will allow be to use my skills to help the company be successful, as well as being satisfied
Clinical Regulatory Affairs
Regulatory Affairs, Government Relations, Strategy
Agricultural Technician
Tags for this Online Resume: Document Control, Records/Information Mgmt, Regulatory Affairs, Quality Assurance, Consulting, Technical Operations
Agricultural Technician
Tags for this Online Resume: biotechnology, plant pathology, microbiology, regulatory affairs
Clinical Research
Tags for this Online Resume: Scientist, Regulatory Affairs, Life Sciences, Research, Medical Writing, Medical Affairs
Clinical Research Associate, Clinical Research Coordinator, Houston
A high-energy and peak-performing, Senior Clinical Research Associate with 15+ years experience ub field monitoring, Regulatory Affairs, QA, QC looking to obtain a contract or full time monitoring or regulatory position with a pharamaceutical, device or biotech company.Certified CRA- SoCRA; certified Regulatory Affairs Specialist certied by RAPS.
