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Online Resumes with "Regulatory Submission"



Traffic/Project/Promotional Communications Manager

Looking for a job with a stable company where I can contribute my skills and knowledge as well as learn.

Tags for this Online Resume: traffic, Project Manager, Promotional Communications, Marketing Communications, Pharmaceutical, Advertising, Marketing, Med/Legal Review, DRA

OPERATIONS / QUALITY ASSURANCE / SAFETY MANAGEMENT

Over 18 years of top performance in optimizing operations for up to 60K+ SF R&D facilities. A peak performer in establishing operational excellence in all facets of pre-clinical studies, encompassing best practices for quality, safety, compliance, and cost control. Adept at managing quality assurance for studies supporting pharmaceutical/biotech regulatory submissions by conducting independent audits, issuing audit reports...

Tags for this Online Resume: Operations Manager, Animal Research, GLP, Safety, Validation, FDA

Administrator, clerk, Regulatory Submission Specialist

Full time with benefits

Tags for this Online Resume: Administrator, Clerical, Regulatory Submission Specialist

Clinical Product Development Professional

As a results-driven professional with expertise spearheading the vision, development, and launch of revenue-producing opportunities in the medical device industry, I am currently looking for my next challenge. I offer exceptional experience in product development, clinical development, regulatory affairs, commercialization, and global launch. With my broad experience and hands-on approach to team building and management, ...

Tags for this Online Resume: clinical, biotech, medtech, operations, medical device, 510k

Medical Technology Executive

As a results-driven professional with expertise spearheading the vision, development, and launch of revenue-producing opportunities in the medical device industry, I am currently looking for my next challenge. I offer exceptional experience in product development, clinical development, regulatory affairs, commercialization, and global launch. With my broad experience and hands-on approach to team building and management, ...

Tags for this Online Resume: Executive, Medical Device, Biotech, Clinical, Regulatory, Operations

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

Regulatory Affairs Associate, New Jersey

Regulatory Affairs professional with a strong regulatory and compliance foundation, well-versed in the laws, regulations and requirements of the FDA; over six years of experience as an International Coordinator for a pharmaceutical organization, currently completing a graduate degree in Regulatory Affairs in Drug Development, Biologics and Medical Devices, studying all facets of regulatory requirements including processes a...

Healthcare information specialist

Healthcare information professional with over 20 years experience working in the pharmaceutical industry looking for new career opportunity in sales, customer service, information services, etc. I have experience answering time-sensitive requests from both Medical R&D issues related to due diligence, adverse event reporting, FDA drug safety response letters and regulatory submissions, as well as the commercial side of Mark...

Featured Profile

Pharmaceutical Program Manager Consultant

Global Leadership, communication, strategy, motivation, coaching, Simultaneous regulatory submission(s), project management

Ideal Companies: Open

Admissions Director

Global Clinical Trials, Executive Coordinator, POC Regulatory Submission Expert Principal Investigator, Professional Assistant

Regulatory Affairs Associate

To obtain a full time position, successfully apply my knowledge and experience in order to achieve excellence in the field of regulatory affairs ensuring personal and organizational growth

Tags for this Online Resume: regulatory affairs, clinical, QC/QA, regulatory submissions, regulatory compliance, drugs, biologics, medical devices