Skip to content

Job Openings

Regulatory Sciences and Medical Writing

Ready to make a difference? Explore our job opportunities in Regulatory Sciences and Medical Writing today! Dive into a dynamic industry that plays a crucial role in shaping the future of healthcare. Join a sector that thrives on innovation, making a significant impact on society while offering immense job satisfaction. Embrace growth opportunities, where your skills are valued, and your contributions drive positive change. Take the next step in advancing your career and discover the exciting possibilities that await in Regulatory Sciences and Medical Writing. Apply now!

Regulatory Specialist II

Alameda, CA 94502

Posted: 04/02/2024 Employment Type: Contract Job Category: Regulatory Sciences and Medical Writing Job Number: 602017 Is job remote?: No Country: United States

Job Description

List 3-5 hard requirements for the role: Responsible for regulatory activities, including product registrations, impact assessment, etc. Understand country-specific requirements and deliver those to internal stakeholders, including product management, engineering, labeling, etc., for product registration and change planning. Communicate weekly with affiliate RAs in different time zones to catch up on ongoing projects and discuss the issues to solve. Plan and execute the given tasks proactively in a timely manner. Report the status to a manager weekly. Keep the training records up to date to do the tasks. List any preferred requirements that would stand out on a resume: understand technical sections (risk management, product change control, biological evaluation)

Years of experience required: 5+

Required education level/certifications: BS, MS Daily tasks/duties and department interactions: prep submissions, regulatory strategy, review change control, other assigned tasks. Interacting with QA, Labeling, Engineer, PMO. Etc.

Description of work environment/department: Assigned Desk, quiet area but dynamic work, Occasional night calls (after 5PM) with Affiliates.

Years Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function

Skills: Knowledge of regulations and standards affecting IVDs and/or biologics

Education: BS preferred in a technical discipline like biology, chemistry, microbiology, immunology, medical technology, etc.

Duties: Responsible for implementing and maintaining the effectiveness of the quality system. Supports manufacturing/operations day to day activities for change control. Provides consultation/advice to regulatory specialist for change control and product development. Provides regulatory direction/interpretation on team activities. Interprets and applies regulatory understanding to support of products and teams. Prepares U.S. regulatory submissions and/or registration documents for international affiliates and government agencies worldwide. Handles regulatory activities involved in documentation,labeling,field support. Applies regulatory and technical knowledge to a wide variety of complex work assignments. Maintains and ensures compliance to the appropriate quality system for the specific medical device(s) designed or manufactured that the individual supports. Ensures compliance to and is able to demonstrate knowledge of site and division level policies and procedures.
Apply Online

Send an email reminder to:

Share This Job:

Related Jobs:

Login to save this search and get notified of similar positions.

Although this hasn't been an issue at Planet Pharma, the staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.

Wordpress Social Share Plugin powered by Ultimatelysocial