Regulatory Affairs Manager

IntelliPro Group Inc.
Sunnyvale, CA, US
$100K-$150K a year
Full-time

Job Description

Job Description

Position - Sr. Regulatory Affairs Manager

Location - Sunnyvale, CA

Full time

Salary - $100k - $150k + Benefits

Bachelor’s degree in Science, Engineering, Math, a medical field, or an equivalent educational background with a focus on technical writing, scientific methodologies, and problem-solving.

Roles and Responsibilities

Can be independently responsible for 510(k) submissions

In this role, you will be part of the regulatory team responsible for proper oversight of medical device development and market introduction.

You will work closely with Quality, Engineering, Product Management, Marketing, and Sales teams to perform regulatory pre- and post-market analysis, and implement and maintain an ISO 13485 and FDA compliant Quality Management System.

Participate in the preparation and review of regulatory submissions to the US FDA and international (outside the US) regulatory authorities.

Support government interactions pertaining to medical device registrations and licensing;

Participate in the development of regional regulatory strategy and update strategy based on regulatory changes.

FDA 510k and EUA application

Provide regulatory support to cross-functional product development and project teams throughout the product lifecycle.

Support regulatory activities required for MDR compliance.

Requirements

A minimum of 5 years of experience in medical device Regulatory Affairs, showcasing a comprehensive understanding of regulatory frameworks.

Demonstrated ability to manage small projects, displaying exceptional organization, independence, and outcome-driven focus.

Outstanding analytical and communication skills, paired with a strong sense of teamwork and meticulous attention to detail.

About Us :

Founded in 2009, IntelliPro stands as a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart.

With a dynamic presence in the USA, China, Canada, Singapore, Philippines, UK, India, Netherlands, and Germany, we continue to lead the way in global talent solutions.

IntelliPro, a global leader in connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations.

As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status.

Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants.

Learn more about our commitment to diversity and inclusivity at https : / / intelliprogroup.com / .

Compensation : The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more.

Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility

Powered by JazzHR

USFw9SzNBe

11 days ago
Related jobs
Promoted
International Flavors and Fragrances
Palo Alto, California

The Associate Regulatory Affairs Manager will be responsible for completing the regulatory work for the Health and Biosciences business and applicable joint ventures, with a focus on food applications, for the U. The The Associate Regulatory Affairs Manager is responsible for regulatory document dev...

Promoted
IntelliPro Group Inc.
Sunnyvale, California

Regulatory Affairs Specialist/Manager will oversee medical device development and market introduction, ensuring compliance with regulatory standards for Class I, II, and III devices. Regulatory Affairs Specialist / Manager. A minimum of 5 years of experience in medical device Regulatory Affairs, sho...

Promoted
Ihealth Labs Inc
Sunnyvale, California

A minimum of 5 years of experience in medical device Regulatory Affairs, showcasing a comprehensive understanding of regulatory frameworks. Participate in the preparation and review of regulatory submissions to the US FDA and international (outside the US) regulatory authorities. Participate in the ...

Promoted
IntelliPro Group Inc.
Sunnyvale, California

A minimum of 5 years of experience in medical device Regulatory Affairs, showcasing a comprehensive understanding of regulatory frameworks. CF; Participate in the preparation and review of regulatory submissions to the US FDA and international (outside the US) regulatory authorities. CF; Partic...

BlossomHill Therapeutics, Inc.
CA, United States

Reporting to the Senior Director of Regulatory Affairs, the Manager/Senior Manager, Regulatory Affairs will be responsible for strategic and administrative aspects of regulatory submissions and life cycle management, ensuring that submissions are in support of company goals, of highest quality, and ...

Katalyst Healthcares & Life Sciences
Menlo Park, California

Regulatory Affairs in the biotechnology or pharmaceutical industries. Manages most aspects of company regulatory interface with domestic and international health authorities. Manages the development and deployment of the regulatory program that ensures aggressive product approval. Manages and may ge...

Gilead Sciences, Inc.
Foster City, California

Provides regulatory advice, making reasoned decisions on regulatory issues for which there may not be clear/specific regulatory guidance. CMC regulatory activities and related regulatory initiatives. Ability to remain current on CMC regulatory intelligence including guidelines and regulatory trends,...

Katalyst Healthcares & Life Sciences
Foster City, California

Liaise with colleagues in Regulatory Affairs therapeutics teams, , Regulatory Operations, Regulatory Project Management and third-party local agents to develop filing plans and deliver submissions to agreed priorities and timelines. An in-depth knowledge of ICH and regional CMC regulatory requiremen...

The Fountain Group LLC
Foster City, California

Liaise with colleagues in Regulatory Affairs therapeutics teams, Gilead local Affiliates, Regulatory Operations, Regulatory Project Management and third-party local agents to develop filing plans and deliver submissions to agreed priorities and timelines. Job Title: Senior Manager, CMC Regulatory Af...

Guardant Health
Palo Alto, California
Remote

The Senior Regulatory Affairs Manager will provide direct regulatory support for screening products. Director of Regulatory Affairs and will liaise closely with regulatory and cross-functional teams at Guardant Health to bring innovative diagnostic assays to market and keep them complaint. Support r...