Natus Sensory India is hiring for the position of Regulatory Affairs Specialist in Bengaluru. This is an excellent entry-level opportunity for candidates looking to begin a career in medical device regulatory affairs, quality assurance, regulatory submissions, product registrations, and regulatory compliance.
The company specifically describes this as an entry-level professional role intended for individuals beginning their careers or transitioning into a new field. According to the job description, no or limited prior professional experience may be required, while internships and relevant academic projects can be beneficial.
The Regulatory Affairs Specialist will support the preparation and coordination of regulatory submission packages for new and existing medical device products. Candidates will gain exposure to product registrations, license renewals, annual registrations, labeling compliance, regulatory documentation, audits, inspections, and interactions with regulatory requirements.
For fresh graduates looking for Regulatory Affairs fresher jobs in Bengaluru, this Natus Sensory opening can provide valuable experience within an international medical device organization.
About Natus Sensory India
Natus Sensory develops and manufactures medical devices and software solutions used in screening, diagnosis, and treatment across sensory and neurological healthcare areas. Its products support the diagnosis of disorders involving sensory systems and neural pathways.
The Bengaluru Regulatory Affairs Specialist will work within the company’s Quality Assurance & Regulatory function and contribute to maintaining regulatory compliance for medical device products.
Key Responsibilities
As a Regulatory Affairs Specialist at Natus Sensory, your responsibilities may include:
- Coordinate and prepare documentation packages required for regulatory submissions.
- Support regulatory submissions for both new and mature medical device products.
- Help ensure compliance with applicable local and regional registration requirements.
- Compile documents and supporting materials required for product submissions.
- Assist with license renewals and annual product registrations.
- Support regulatory compliance related to product labeling, manufacturing, marketing, and clinical protocols.
- Assist with regulatory tracking and control systems.
- Stay updated on applicable regulatory procedures and regulatory changes.
- Support internal audits and regulatory inspections.
- Assist experienced regulatory professionals with defined regulatory agency matters.
- Contribute to strategies supporting timely regulatory and clinical trial application approvals.
- Follow established procedures and structured problem-solving methodologies.
- Identify potential issues or abnormalities and escalate them to experienced team members when required.
- Communicate clearly with colleagues and provide factual responses.
- Complete assigned projects according to established requirements and timelines.
- Inform leadership promptly about potential delays or issues.
- Collaborate with cross-functional and international teams.
- Support continuous improvement while maintaining a patient-focused approach.
Who Can Apply?
This position is explicitly described by Natus Sensory as an entry-level professional opportunity for candidates who have recently completed relevant formal education or training.
Based on the medical device Regulatory Affairs responsibilities described in the job posting, relevant educational backgrounds may include:
B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc in Life Sciences, Biotechnology, Biomedical Sciences, Biomedical Engineering, B.Tech/BE Biomedical Engineering, Medical Device/Regulatory Affairs-related qualifications, or another relevant scientific/technical discipline.
Important: The supplied job description does not specify a mandatory degree or exact academic specialization. Therefore, candidates should verify their eligibility against the official application form rather than treating the above degree list as an employer-mandated requirement.
Is This Job Suitable for Freshers?
Yes. This role is suitable for freshers and early-career candidates.
The job description clearly states that this level is intended for people beginning their professional careers or transitioning into a new field.
Natus Sensory further notes that:
- No or limited prior professional experience may be required.
- Relevant formal education or training is expected.
- Internships may be beneficial.
- Academic projects may be beneficial.
- Employees will receive structured guidance and oversight.
- The position is designed to build foundational professional experience.
This makes the Natus Sensory Regulatory Affairs Specialist opening particularly relevant for candidates searching for Regulatory Affairs jobs for freshers in Bengaluru or entry-level opportunities in the medical device industry.
Skills That Can Help Candidates
Although the role is designed for entry-level professionals, candidates with knowledge of the following areas may have an advantage:
- Regulatory Affairs fundamentals
- Medical device regulations
- Regulatory documentation
- Product registration and submissions
- Quality Assurance principles
- Labeling compliance
- Document control
- Regulatory audits and inspections
- Clinical research fundamentals
- Good Documentation Practices
- Microsoft Office and documentation skills
- Written and verbal English communication
- Attention to detail
- Teamwork and collaboration
- Time management
- Basic problem-solving skills
Candidates are not necessarily expected to have professional mastery of these areas, as the position focuses heavily on learning and professional development.
Work Location and Work Model
The position is associated with Bengaluru, Karnataka, India.
An important point for applicants is the work arrangement. According to Natus Sensory, the role will initially start as a work-from-home position but is expected to transition into an office-based role in Bangalore.
Candidates should therefore be prepared to work physically from Bengaluru when the company transitions the position to its office.
Travel requirements are minimal at less than 5%.
Salary for Natus Sensory Regulatory Affairs Specialist
Natus Sensory has not disclosed a specific salary range in the supplied job posting.
For informational purposes, an estimated market-aligned range for an entry-level Regulatory Affairs position in Bengaluru may be approximately:
₹3,50,000 – ₹6,00,000 per year
This is an editorial estimate and not an officially disclosed Natus Sensory salary range. Actual compensation can vary based on education, skills, prior internships, relevant experience, internal compensation structure, and the final offer.
Benefits
Selected candidates may receive:
- Competitive salary
- Performance-based incentives
- Medical insurance coverage for employees and their families
- Gratuity according to applicable statutory norms
- Paid time off according to applicable labor laws
- Initial work-from-home arrangement
- International and collaborative working environment
- Exposure to different cultures and global teams
- Professional learning and career-development opportunities
- Minimal travel requirements
- Structured support for early-career professionals
Why Consider This Regulatory Affairs Opportunity?
For candidates trying to enter the medical device industry, this position provides exposure to several core areas of Regulatory Affairs and Quality Assurance.
The opportunity can be particularly relevant for candidates interested in developing careers in regulatory submissions, medical device regulatory affairs, regulatory operations, product registration, regulatory compliance, labeling, quality systems, or related functions.
Because the company explicitly positions the vacancy at an entry level, fresh graduates who have theoretical Regulatory Affairs knowledge, internships, academic projects, or relevant scientific education should consider reviewing the opening.
How to Apply
