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Regulatory Affairs Specialist, Sunnyvale, CA

Kelly

This is a Full-time position in Sunnyvale, CA posted June 11, 2021.

Regulatory Affairs Specialist, Sunnyvale, CA

Location: Sunnyvale, CA

(This will be an onsite position)

Term: 1 year contract opportunity

The Regulatory Affairs Specialist will prepare the regulatory submissions and interact with Distributors, Regulatory Agencies and Health Authorities to obtain and maintain product approvals.

ESSENTIAL JOB RESPONSIBILITIES:
Prepare regulatory submissions for countries with focus on Latin America region Communicates with in-country Regulatory Affairs personnel to facilitate global clearances/approvals.

Coordination with department personnel from regulatory, quality, and manufacturing sites, sales and marketing.

Interact with global regulatory leaders and peers to expedite approval of pending registrations.

Organizes and maintains files such as Responsibilities Matrix, Certificates from Notified Bodies CFS and CFG and other RA related material.

Regulatory review and approval of design, manufacturing, labelling, packaging-related changes in compliance with applicable regulations and providing Regulatory Change Assessments through RCA .

Prepare formal written reports, PowerPoint presentations, and documents for distribution within work unit and regions.

Education and Experience in years:
Bachelor’s degree in Life Science or related field with 2+ years of Quality or Regulatory experience -OR
– Master’s degree in in a Life Science or related field with 1-2 years of Quality or Regulatory work experience
Knowledge and skills:
Demonstrate in-depth understanding of advanced technical/scientific principles that relate to multiple, diverse, and or complex product lines or manufacturing processes Ability to interpret subjective and complex aspects of specific regulations and has thorough understanding of multiple sets of associated regulations IVD product experience is highly preferred Prior knowledge of different databases like Trackwise, Agile documentation system is preferred.

Experience in regulatory/Quality or related departments within an IVD or medical device industry Fluency in Spanish preferred

Why Kelly ® ?

Kelly® Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you.

Every day, we match science professionals with dream jobs that fit their skills and interests-it’s the way we think job searching should be.

Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.

About Kelly ®

At Kelly, we’re always thinking about what’s next and advising job seekers on new ways of working to reach their full potential.

In fact, we’re a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?).

Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity.

Equal Employment Opportunity is The Law.

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