Regulatory Affairs Specialist V

eTeam Inc.

Lake Forest, CA

JOB DETAILS
SKILLS
Biotech and Pharmaceutical, Business Development, Business Strategy, Communication Skills, Consumer Promotions, Cross-Functional, Documentation, Due Diligence, English Language, GxP, International Law, Leadership, Licensing, Maintain Compliance, Materials Tracking, Medical Equipment, Multitasking, Problem Solving Skills, Product Support, Product/Service Launch, Project Tracking, Project/Program Management, Quality Control, Regulations, Regulatory Compliance, Secondary School, Standard Operating Procedures (SOP), Time Management
LOCATION
Lake Forest, CA
POSTED
18 days ago

Job Title:  Regulatory Affairs Specialist V
Job Location - Lake Forest, CA
Duration - 09 months

Job Overview

The role involves setting or executing regulatory strategy, leading and managing as a strategist, ensuring local product registration, facilitating health registration approvals, and supporting the Senior Director during due diligence and integration activities for Business Development & Licensing projects. The candidate will plan and recommend regulatory strategies for pipeline products, actively participate in cross-functional teams, and influence business strategies to address regulatory needs.

Expectations / Responsibilities

  • A self-starter, assertive leader who will be accountable for the end-to-end regulatory support for the anterior/posterior ophthalmologic products, including new products, sustaining legacy products, and improvements to the product lines.
  • Oversee multiple projects within the Regulatory Affairs Strategy team, ensuring goals are met through self-directed work and effective supervision.
  • Coordinate regulatory activities, including product submissions, renewals, and updates, by liaising with plants, agents, and governmental authorities to ensure timely submissions and approvals.
  • Oversee promotional material approval for Client ME/KSA portfolio, ensuring ethical conduct and compliance with national and international laws, codes, and regulations.
  • Provide regulatory strategies for new product introductions and product changes, maintaining regulatory compliance to drive competitive advantage.
  • Support products in the medical device and/or pharmaceutical families, ensuring adherence to all relevant regulations.
  • Make decisions impacting project performance and success, requiring project management, advanced problem-solving, effective communication, and industry-specific knowledge.
  • Adhere to GxP regulations by following Standard Operating Procedures (SOPs), maintaining accurate documentation, ensuring quality control, and completing required training.
  • Meet individual job requirements and contribute to the overall compliance of the organization.

What You’ll Bring to Client

  • Bachelor’s Degree or equivalent years of directly related experience (or high school 15 yrs; Assoc. 11 yrs; M.S. 4 yrs; PhD 3 yrs).
  • The ability to fluently read, write, understand, and communicate in English.
  • 7 years of relevant experience.
  • 5 years of demonstrated leadership.

Additional Information

Location: Onsite, Lake Forest, CA

About the Company

e

eTeam Inc.

Looking for a great job? Join eTeam. We’re looking for talented staffing professionals to join our staff. We also provide contract assignments and full-time jobs at Fortune 2000 Companies. We’ve been named one of the best companies to work for by Staffing Industry Analysts and New Jersey Business.
COMPANY SIZE
100 to 499 employees
INDUSTRY
Other/Not Classified
FOUNDED
1998
WEBSITE
www.eteaminc.com