Regulatory Affairs Specialist Hiring at Vantive

Vantive Hiring Regulatory Affairs Specialist in Bengaluru

Vantive has announced a new hiring opportunity for the position of Regulatory Affairs Specialist at its Bengaluru location. The company is inviting applications from experienced regulatory affairs professionals with expertise in medical devices, healthcare compliance, EU MDR regulations, regulatory submissions, and digital healthcare portfolios.

This recruitment drive is attracting candidates searching for regulatory affairs jobs in Bangalore, medical device regulatory careers, EU MDR compliance jobs, healthcare regulatory specialist openings, digital healthcare regulatory roles, USFDA submission careers, and pharmaceutical compliance opportunities.

Candidates with strong knowledge of regulatory strategy, product registration, global submission management, and healthcare compliance documentation can apply for this opportunity.

Company Overview

Vantive is a global vital organ therapy company focused on advancing kidney care, dialysis innovation, digital healthcare solutions, and vital organ therapy technologies. The company continues to build on its healthcare legacy by developing innovative treatment solutions that improve patient outcomes and healthcare delivery systems.

The organization operates extensively in healthcare technology, medical device innovation, regulatory compliance, patient therapy systems, and digital healthcare transformation. Vantive continues to strengthen its global regulatory affairs operations to support product approvals, compliance management, and international healthcare market expansion.

Medical device and healthcare regulatory sectors continue to generate strong demand for skilled professionals due to evolving EU MDR regulations, healthcare compliance standards, digital health innovations, and global product registration requirements.

Bengaluru remains one of India’s leading healthcare technology and pharmaceutical operations hubs, creating strong career opportunities in medical device regulation, healthcare compliance, clinical operations, digital health systems, and pharmaceutical regulatory affairs.

Job Role & Responsibilities

Regulatory Affairs Specialist Responsibilities

Candidates selected for this role will support regulatory strategy and compliance operations for digital healthcare and medical device portfolios.

Key responsibilities include:

• Identifying regulatory strategies for digital healthcare portfolios
• Supporting sustaining regulatory projects and compliance activities
• Preparing regulatory dossiers for EU and US markets
• Supporting GeoX regulatory submission deliverables
• Planning regulatory activities for EU MDD and MDR compliance
• Obtaining regulatory clearances in target countries
• Coordinating with regulatory authorities for approvals and clarifications
• Responding to regulatory questions and compliance deficiencies
• Coordinating with in-country regulatory teams for registrations and renewals
• Supporting end-of-life regulatory documentation activities
• Maintaining healthcare regulatory compliance documentation
• Supporting global healthcare product registration operations

Skills Required

Candidates should possess:

• Strong regulatory affairs knowledge
• Medical device compliance understanding
• EU MDR and EU MDD regulatory expertise
• USFDA regulatory submission knowledge
• Regulatory dossier preparation skills
• Product registration and market access understanding
• Healthcare compliance documentation abilities
• Communication and stakeholder management skills
• Cross-functional coordination capabilities
• Problem-solving and analytical skills

Candidates with exposure to digital healthcare products, medical device regulations, kidney care technologies, and international regulatory frameworks will have an advantage.

Eligibility / Qualifications

Educational Qualification

Candidates with healthcare, pharmaceutical, biotechnology, and life sciences educational backgrounds are eligible.

Relevant educational qualifications include:

B.Pharm, M.Pharm, Pharm.D, Biotechnology, Biomedical Engineering, Life Sciences, Medical Devices, Healthcare Technology, Regulatory Affairs.

Experience Requirement

• Experience in regulatory affairs preferred
• Medical device and healthcare regulatory exposure preferred
• EU MDR and USFDA submission experience preferred
• Product registration and compliance documentation experience preferred
• Regulatory authority coordination experience preferred

These openings are suitable for:

• Regulatory affairs specialists
• Medical device compliance professionals
• Healthcare regulatory associates
• Digital healthcare compliance professionals
• Product registration specialists
• Pharmaceutical regulatory experts
• Global submission management professionals

Location & Salary

Location

Bengaluru, India

Estimated Salary

₹9 LPA – ₹18 LPA approximately

Salary may vary depending on medical device regulatory expertise, EU MDR exposure, healthcare compliance knowledge, and global submission management experience.

Application Process

Interested candidates can apply through the official Vantive careers portal.

Apply Online

https://jobs.vantive.com/job/-/-/47727/95581213712

Job ID

JR – 194199

Category

General Regulatory Affairs

Frequently Asked Questions (FAQs)

1. What position is Vantive hiring for in Bengaluru?

Vantive is hiring for the role of Regulatory Affairs Specialist.

2. Which qualifications are eligible for this healthcare regulatory role?

Candidates with Pharmacy, Biotechnology, Biomedical Engineering, Medical Devices, and Life Sciences qualifications can apply.

3. What regulatory skills are preferred for this opportunity?

Experience in EU MDR, EU MDD, USFDA submissions, regulatory dossier preparation, and product registration is preferred.

4. What is the estimated salary for Regulatory Affairs Specialist roles?

The expected salary range is approximately ₹9 LPA to ₹18 LPA depending on regulatory expertise and healthcare industry exposure.

5. What is the work location for this opportunity?

The work location is Bengaluru, India.

6. How can candidates apply for Vantive recruitment?

Candidates can apply through the official Vantive careers portal.

Summary Table

Company	Vantive
Department Vacancies	Regulatory Affairs Specialist
Qualification	B.Pharm, M.Pharm, Pharm.D, Biotechnology, Biomedical Engineering, Life Sciences
Experience	Regulatory Affairs & Medical Device Compliance Experience Preferred
Location	Bengaluru, India

Tagged as: Pharma Jobs in Bangalore