Regulatory Affairs Senior Specialist - Supply Chain

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Not verified checked Jun 13, 2026

Salary

Not verified

401(k) match

Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)

$61,842 U.S. median for this role

Projected growth (BLS Employment Projections)

+1.9% - Slower

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function

Operations From the posting source checked Jun 20, 2026

Seniority

Senior From the posting source checked Jun 20, 2026

Work mode

Remote From the posting source checked Jun 20, 2026

In-office days

0 days From the posting source checked Jun 20, 2026

Schedule

Shift type

Not verified

Weekend work

Not verified

Company

Company stage

Public-company From the posting source checked Jun 20, 2026

Equity

Offered Verified - SEC 10-K source checked Jun 20, 2026

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Regulatory Affairs Senior Specialist - Supply Chain Europe UK- Remote It's fun to work in a company where people truly believe in what they are doing! The Regulatory Affairs Senior Specialist plays a key role in ensuring regulatory, quality, and safety compliance across a diverse regional portfolio. In this senior position, you will act as a trusted subject matter expert, partnering with internal teams and external stakeholders to maintain audit readiness, support market access, and uphold the highest standards of regulatory governance across multiple EMEA countries. Key Responsibilities Take site-level responsibility for regulatory compliance and ongoing audit readiness, ensuring documentation, processes, and systems meet relevant EMEA and local regulatory requirements. Manage medical device vigilance and reporting activities within the region in line with applicable EMEA and country-specific regulations, timelines, and procedures. Prepare, review, and maintain regulatory declarations and documentation required for shipping, import, export, and trade into EMEA markets. Ensure local quality assurance activities support compliance with internal quality systems, regulatory standards, and continuous improvement objectives. Oversee country-level product and site compliance, including fulfilment of Extended Producer Responsibility (EPR) and other environmental or stewardship obligations where applicable. Coordinate the creation, review, and maintenance of regional Safety Data Sheets (SDS) and hazard labelling to ensure alignment with relevant chemical, safety, and transport regulations, and maintain accurate records of local registrations, approvals, certifications, and licences. Job Requirements Proven experience in regulatory affairs within the medical device, pharmaceutical, or related life sciences sector, with demonstrable exposure to EMEA markets. Strong working knowledge of

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