Oceanside Jobs

The Clinical Trials Regulatory Research Associate is responsible for the development and maintenance of regulatory docum ... is the preparation of clinical trial protocols and related regulatory documents for submission to the UCSD Human...

Develops domestic and international strategies for regulatory approval of company products Researches and ... Demonstrated proficiency with relevant US/International regulatory requirements for medical devices including...

Writer/Manager, Regulatory Writing, to join the team. Interested parties can review the job description and apply on-line ... Support the timely generation of high-quality regulatory documentation by assuming other duties, including...

Writer/Manager, Regulatory Writing to join the team. Interested parties can view the job description and apply on-line at: ... Support the timely generation of high-quality regulatory documentation by assuming other duties, including...

Position Summary: Under minimal supervision, the Senior Regulatory Affairs Specialist supports the Regulatory ... regulatory premarket approval applications to worldwide regulatory agencies Ensures regulatory submissions are...

We have an Associate level Regulatory Affairs position open. The position is contract (temp) but available to interview ... position for someone in QA or just starting their career in Regulatory Affairs. DUTIES AND RESPONSIBILITIES: Extract...

Responsible for researching and executing regulatory tasks of moderate scope, complexity and risk. Performs regulatory ... to all regulatory requirements. Supports in administrating regulatory training programs. Responsibilities: * Draft and...

Extract registration market approval status from various country folders, associate the findings with our products and part numbers for spreadsheet entry and upload into Oracle. DUTIES AND RESPONSIBILITIES: Review historical and current...

Regulatory Affairs and Quality Systems. The Sr. Manager, Regulatory Affairs and Quality Systems is responsible for ... development and manufacturing phases. * Responsible for regulatory approvals from FDA and foreign regulatory...

responsibilities include developing and executing global regulatory CMC strategy. Provides leadership in coordinating ... supplements and commitments. Development and execution of regulatory plans (filing strategies, preparation, submission...