Thank you for your interest in our job posting! We're thrilled to see your enthusiasm and would love to explore this opportunity with you further.

To dive deeper into what this role can offer, feel free to reach out to me directly. You can connect with me, Chitrank Rastogi, on LinkedIn (https://www.linkedin.com/in/chitrank-rastogi-55119a102/) for a professional introduction.

If you prefer, you can also email me your updated resume at chitrank.rastogi@collabera.com, or simply give me a call at (425) 523-1648. I'd be happy to discuss how your skills and experiences align with our needs at your earliest convenience.

Pay Range - $35 to $40/hr. (negotiable)

Job Description:
Job Roles & Responsibilities:

Description / Summary:
This role will provide support to the Regulatory Affairs organization by –

• Monitoring changing regulations (emerging regulatory issues, trends) in rest of the world geographies and translating regulatory requirements into the quality system,
• Driving implementation of new international regulatory requirements, ensuring procedures are current and regulatory requirements and guidances are met,
• Fulfilling international submission deliverables for product registration renewals and for regulatory emerging issues where multiple medical devices require submission, including maintaining tracker of Declarations of Conformity, confirming against local requirements, and driving to issuance.
• Driving quality system process improvement initiatives

Initiatives include but are not limited to:

• Establishing emerging issues in our quality system,
• Maintaining the quality system procedures (e.g. change management),
• Liaising with cross-functional partners, distribution centers, and international affiliates to obtain/align on international regulatory requirements,
• Troubleshooting with regulatory affiliates, and
• Participating in RA projects.
• Role has a potential for investigating nonconformances (CAPAs) and implementing mitigations.
• Exposure to Quality Systems, a Quality role, or a Compliance role is a plus.

 Pan Franchise Specialist – Santa Clara

List of tasks:

• CFG requests in the FDA database.
• Declarations of conformity.
• Review Regulatory Letters and maintain LoA / PoA tracker.
• Will coordinate pan-franchise requests for multiple products, schedule meetings with international requesters.
• Maintain tracker / SharePoint / folders with current state.
• Change management

Skills:

• Independent
• Troubleshooting
• Critical thinker
• Ability to drive a problem through resolution and implement mitigations.
• Ability to handle multiple streams simultaneously.