Global Regulatory Manager – Contract

Frida

Global Regulatory Manager at Frida ensuring compliance in CPG and medical device sectors globally. Managing regulatory responsibilities for product sourcing, development, and manufacturing.

Posted 5/14/2026contractRemote • Oregon • 🇺🇸 United StatesMid-LevelSeniorWebsite

About the role

Key responsibilities & impact

Manage the development and implementation of regulatory strategies and plans to support the timely introduction of new products and the preparation/review of international regulatory submission(s) (EU MDR Tech File, Health Canada submission, Saudi FDA, etc)
Represent international regulatory interests on cross-functional project team for new and existing products
Review and approve labeling requirements for global market(s); translation material, claims review, IFU, etc.
Evaluate change proposals for international regulatory impact
Maintain effective communication within the RA/QA group, as well as, cross-functional business partners, i.e. Product Development, Marketing, Legal, etc.
Support Regulatory and Quality Departments efforts in maintaining ISO 13485 and MDSAP Certifications (internal audit, NB audits, SOP compliance, etc)
May provide direct supervision of individual(s)

Requirements

What you’ll need

Bachelor's degree in Science, Engineering, Pharmaceutical discipline(s)
Direct experience with international regulatory affairs (submissions, License renewals, TF, etc.)
A minimum of 3 years in a medical device, pharmaceutical or similar organization
Ability to handle competing priorities and deadlines
Highly organized, meticulous with a great attention to detail
Able to work independently as well as in teams
Result-oriented, creative and able to multitask
Great communication skills both verbally and written
Ability to work in a fast-paced environment in which requirements & priorities constantly change
Excellent written and verbal communication
Consumer obsessed and possess strong consumer understanding
Excellent communicator with strong written, verbal, and presentation skills
Ability to manage multiple projects at once and strong organizational skills
Proactive; can operate autonomously, but also collaboratively as part of a team

Benefits

Comp & perks

Comprehensive medical, vision, and dental plan options
Employer paid life insurance
Supplemental insurance options including Accident Insurance, Short-Term Disability and Long-Term Disability, Cancer Coverage, and more
FSA & HSA
401k matching up to 4% with immediate vesting
Generous paid time off program including elective PTO days, federal holidays, sick/wellness days, floating holidays, and a birthday day off!
Pregnancy and parental leave
Weekly wellness programming in-office
Dog friendly office - feel free to bring your best buddy with you to work!
Learning & development opportunities for professional and personal growth
Company-wide events & outings. Team engagement is at the center of our culture. This ranges from small department-specific teambuilding or informal outings to our annual Fam Jam family carnival that celebrates the people in your life who support you in bringing your best self to work each day. We also host an annual Day of Service to support our local Miami community, and provide a variety of volunteer opportunities throughout the year that support our mission to serve parents and children.
Exclusive employee product discounts

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

regulatory strategiesinternational regulatory submissionslabeling requirementsISO 13485MDSAPinternal auditSOP compliancemedical device regulationspharmaceutical regulationschange proposals evaluation

Soft Skills

communication skillsorganizational skillsattention to detailability to multitaskresult-orientedcreativityability to handle competing prioritiesindependenceteam collaborationproactivity