Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices in Hyderabad for freshers and 0–2 years experience candidates.
Introduction
Candidates who want to start their careers in medical device regulatory affairs can explore this opportunity at GRK Medical Devices Private Limited. The company is currently recruiting for the position of Regulatory Affairs Executive at its facility located in Hyderabad, Telangana.
This role is suitable for freshers and early-career professionals with 0–2 years of experience who have completed degrees in Pharmacy, Biomedical Engineering, or related engineering disciplines. The selected candidate will assist in regulatory documentation, product registration activities, and compliance with international medical device regulations.
Working in regulatory affairs within the medical device industry offers valuable experience in global compliance standards, regulatory submissions, and quality management systems. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Company Overview
GRK Medical Devices Private Limited operates in the medical device manufacturing sector, focusing on developing and supplying healthcare products that meet regulatory and quality standards. Companies in the medical device industry must comply with strict regulatory frameworks to ensure product safety and effectiveness before they reach healthcare providers and patients.
The regulatory affairs team within such organizations plays an important role in preparing documentation, maintaining compliance with global standards, and supporting product registrations in different markets.
Professionals working with GRK Medical Devices gain practical exposure to regulatory systems, technical documentation, and compliance processes used in the medical device industry. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Job Overview
| Job Details | Information |
|---|---|
| Company Name | GRK Medical Devices Private Limited |
| Job Role | Regulatory Affairs Executive |
| Industry | Medical Devices |
| Job Location | Hyderabad, Telangana |
| Employment Type | Full-Time |
| Experience Required | 0 – 2 Years |
| Qualification | B.Tech / M.Tech / B.Pharm / M.Pharm / Biomedical Engineering |
| Application Mode | Email Application |
Job Location & Employment Type
The Regulatory Affairs Executive position is based in Hyderabad, Telangana, at the company’s facility located in ALEAP Industrial Estate, Pragathi Nagar.
This is a full-time role within the regulatory affairs and compliance department. The selected candidate will support regulatory documentation and compliance activities related to medical devices. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Open Positions / Department Details
Position: Regulatory Affairs Executive
Department: Regulatory Affairs / Compliance
The regulatory affairs department ensures that medical devices meet regulatory requirements and quality standards before they are marketed or distributed. Professionals working in this department prepare documentation, manage product registrations, and ensure compliance with international regulatory frameworks. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Key Roles & Responsibilities
Regulatory Documentation Preparation
The selected candidate will assist in preparing regulatory documentation and technical files required for medical device approvals.
These documents are essential for regulatory submissions and product certification processes.
Compliance with Regulatory Standards
The role involves supporting compliance with regulatory requirements applicable to medical devices. This includes ensuring that documentation aligns with international quality and regulatory standards.
Product Registration Support
The Regulatory Affairs Executive may assist in activities related to product registration and regulatory approvals for medical devices in different markets.
Quality Management System Documentation
Maintaining regulatory documentation in accordance with ISO 13485 Quality Management System standards is a key responsibility.
This ensures the company’s processes align with international quality requirements for medical devices.
Coordination with Internal Teams
The candidate will collaborate with internal teams such as quality assurance, manufacturing, and research departments to gather documentation required for regulatory submissions.
Regulatory Audit Support
The role may involve assisting with internal and external regulatory audits by preparing documentation and supporting compliance reviews.
Regulatory Updates Monitoring
Keeping track of updates in medical device regulatory frameworks and guidelines is important to ensure compliance with evolving regulatory requirements.
Eligibility Criteria
Candidates interested in applying for this role should meet the following requirements.
Education
Applicants must possess one of the following qualifications:
- B.Tech or M.Tech
- B.Pharm or M.Pharm
- Biomedical Engineering
These educational backgrounds provide the technical knowledge required for regulatory affairs roles in medical devices.
Experience
- Freshers or candidates with 0–2 years of experience are eligible to apply.
Candidates who have completed internships in medical device companies may have an advantage. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Technical Knowledge Requirements
Candidates should have basic knowledge of the following medical device standards:
- ISO 13485 – Quality Management Systems for Medical Devices
- ISO 14971 – Risk Management for Medical Devices
- ISO 11135 – Sterilization of Medical Devices
- ISO 10993 – Biocompatibility Evaluation of Medical Devices
Understanding these standards helps ensure medical devices meet international regulatory requirements. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Preferred Knowledge
Candidates with knowledge of the following regulatory frameworks may have an advantage:
- EU Medical Device Regulation (MDR)
- US FDA medical device regulatory pathways
- CE Marking requirements
These regulatory frameworks govern the approval and distribution of medical devices in global markets. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Skills Required
Successful candidates should possess the following skills:
- Regulatory documentation and compliance knowledge
- Understanding of medical device regulatory standards
- Attention to detail when preparing regulatory documents
- Ability to work collaboratively with cross-functional teams
- Strong analytical and communication skills
Salary & Benefits
The salary package for this role has not been publicly disclosed and will be as per company norms.
Employees working in regulatory affairs roles may benefit from:
- Entry into the medical device regulatory affairs field
- Exposure to international regulatory frameworks
- Experience working with quality management systems
- Career growth opportunities in regulatory affairs, compliance, and quality assurance
Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Selection Process
The recruitment process may include the following steps:
- Resume Screening
- Technical Interview
- HR Discussion
- Final Selection
Shortlisted candidates will be contacted by the company’s recruitment team. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
How to Apply
Candidates interested in the Regulatory Affairs Executive role at GRK Medical Devices can apply by sending their updated resume through email.
Email Application
Applicants should mention the subject line:
“Application for Regulatory Affairs Executive – GRK Medical Devices”
Providing relevant academic or internship experience related to regulatory affairs can improve the chances of being shortlisted. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Important Dates
- Job Posted: March 15, 2026
- Application Deadline: Not specified
Candidates are advised to apply at the earliest. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Why Apply for This Pharma Job?
Regulatory affairs in the medical device industry is a rapidly growing field that focuses on ensuring healthcare products meet global safety and quality standards. Professionals working in this area develop expertise in regulatory documentation, product approvals, and compliance management.
Starting a career as a Regulatory Affairs Executive allows candidates to gain experience in global regulatory frameworks and quality management systems used in the medical device sector. This experience can lead to career growth in regulatory strategy, quality assurance, and compliance roles within the healthcare industry.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform that publishes pharmaceutical and healthcare job updates for informational purposes only.
We do not conduct recruitment or charge any fees for job applications. Candidates should verify job details directly with the company before applying. IndiaPharmaJobs.in is not affiliated with GRK Medical Devices Private Limited or any other organization mentioned in the job postings. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
Final Call-to-Action
Candidates interested in building a career in medical device regulatory affairs should consider applying for this opportunity. Send your updated resume to the provided email address and highlight your educational background, regulatory knowledge, or internship experience to improve your chances of being shortlisted for the Regulatory Affairs Executive role at GRK Medical Devices in Hyderabad. Regulatory Affairs Executive Jobs for Freshers at GRK Medical Devices
