Regulatory Affairs Senior Specialist

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Offered From the posting source checked Jun 20, 2026
• 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)

Was this benefit information wrong? Tell us.

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

Onsite From the posting source checked Jun 20, 2026

In-office days

5 days From the posting source checked Jun 20, 2026

Schedule

Shift type

Not verified

Weekend work

Not verified

Company

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 Gurgaon, Haryana, India Regulatory Affairs Senior Specialist Gurgaon, Haryana, India (On-site) TRENDING JOB DESCRIPTION Support new product registrations and license renewals for medical device and fertility products in India, Sri Lanka, and Nepal, ensuring compliance with applicable local regulatory requirements. Act as the primary regulatory liaison with external consultants, distributors, and local health authorities, coordinating all regulatory‑related communications, submissions, responses, and follow‑ups. Ensure timely progression of regulatory activities, proactive issue resolution, and alignment between internal stakeholders and external parties to support uninterrupted market access and regulatory compliance. RESPONSIBILITIES Provide regulatory input and guidance for assigned countries on regulatory‑related matters. Ensure product registrations are reviewed, maintained, and renewed in accordance with local regulatory requirements. Provide regular updates to the management team on product registration and renewal status and proactively propose action plans in the event of delays. Collaborate closely with regional and global teams on regulatory documentation and Regulatory Information Management Systems (RIMS). Prepare, coordinate, and submit regulatory applications to local health authorities and/or distributors, as appropriate. Support regulatory strategy development for new products, product changes, and market expansions in assigned countries. Track and monitor regulatory timelines and commitments, escalating risks and constraints proactively to minimize delays. Coordinate with Quality, Manufacturing, Supply Chain, and Commercial teams to ensure regulatory compliance and uninterrupted product supply. Maintain awareness of local regulatory updates, guidelines, and new regulations, including their implementation and impact on the business. Establish and maintain relationships with local medical device industry associations and participate in discussions on

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