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Online Resumes with "regulatory strategy"

Regulatory Affairs Associate

To provide regulatory support for FDA product applications and submissions and for effective and successful implementation of regulatory strategies.

Director, Regulatory Compliance

A regulatory position where I can use my expertise in managing the product development cycle, submission, launch and post marketing phases and my proven ability in regulatory strategy to bring products to market in a timely manner.

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Senior Director, Chicago

To obtain a leadership position for regulatory affairs expertise in the pharmaceutical/biotech industry

Tags for this Online Resume: regulatory affairs, pharmaceutical, biotechnology, clinical , manufacturing

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Strategic Customer Operations Executive

I'm seeking a customer-driven environment committed to achieving a high level of performance. The strategy I employ is to make the best use of critical resources to lower negatives like turnover rates, teach my direct and indirect reports to manage more effectively and incorporate the vision of the call center with the organization’s vision. I work to develop a culture that produces the highest level of performance by mak...

Ideal Companies: Small to medium sized technology driven operating companies

Tags for this Online Resume: Customer, Client, Centralize, Contact, Technology, Leader

Quality Assurance and Regulatory Affairs Professional - NJ

Domestic and international regulatory strategy to market (medical device, pharmaceutical, combination and consumer products). Implement quality management systems; prefer start-up or small company environment where there is a lot of building (not maintaining) to do.

Tags for this Online Resume: CAPA, FDA, change control, PMA, complaint, CE Mark

Senior Biotechnology Executive

seeking opportunity in leading the development of new therapeutics, imaging contrast agents, innovative imaging devices that are combined with therapeutic devices.

Tags for this Online Resume: Biomarkers, Translational Medicine, radiology, Neurology, Oncology, regulatory strategy

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PhD Research Scientist With 12+years of Experience in Biomedical Sciences

I am seeking opportunities to contribute as a scientist within preclinical drug development or drug discovery research for the bio-pharmaceutical industry to support the primary or secondary screening and characterization of the molecular mechanism of action of lead drug candidates enabling target validation. I specialize in the development of cell-based assays using genomic, proteomic and biochemical approaches implementin...

Ideal Companies: Biogen Idec, Joule Scientific, Novartis NIBR, Aveo Oncology, Agios, Pfizer, Millipore, Merck, EMD serono, Third rock ventures, Cambridge Scientific, Alkermes, Enlight Biosciences

Tags for this Online Resume: Lentiviral Retroviral shRNA RNA knockdown screens, Flow Cytometry, RTPCR, Immunopreciptations, Reporter assays, Cell based Assays, ELISA, Migration, Stable and Transient Transfections, Genomic and Proteomic Studies, Cloning, Transient siRNA knockdowns, Phenotyping Mammalian cell lines, Gene Overexpression, Subcloning to expression Vectors, Construct Stable Inducible Cell lines, Protein Kinase Assay, Pulse Chase Experiments, Transfection, Transduction, Transformation, Polyoma virus DNA tumor virus replication, Research Scientist, Cell Biology Protein Biochemistry Genetics Molecular Bioliogy Oncology Virology, FACS

Energy/Utility Regulatory Attorney, Executive 20 years

I possess significant legal, regulatory and legislative advocacy and management experience in the utility and energy industries. I have developed federal, state and regional energy legislative and regulatory strategies on behalf of Fortune 500 investor-owned utilities, and energy and transmission developers. During this time, I have provided a variety of legal, public policy, legislative and regulatory advocacy services in...

Tags for this Online Resume: Utility Government Affairs professional, Energy regulatory, experienced energy attorney , renewable energy advocate

Quality Coordinator - 20 Years of Experience - Near L5B4A1

A qualified experienced Regulatory Affairs professional with a rich career full of success in regulatory affairs, projects management, Good Manufacturing practice guidelines (GMP) and pharmaceutical sites auditing. Provide good direction and experienced to lead Product Regulation Managers and Associates to develop and implement the regulatory strategies and processes to assure timely global commercialization of products in ...