Find Your Dream Radiology Job in India

Job Title:

RA & QA Engineer - Regulatory & Safety (Radiology & Imaging Systems)

Department:

Regulatory & Safety - Radiology Division

Location:

Vapi, Gujarat

Reports To:

Manager / Senior Manager.

Job Purpose:

To manage and coordinate regulatory documentation and compliance activities for radiology and imaging systems such as X-Ray, C-Arm, Digital Radiography (DR), and CT equipment, ensuring adherence to BIS, AERB, NABL, and international regulatory standards applicable to medical device manufacturing.

Key Responsibilities:

1. Regulatory Documentation and Compliance

• Prepare, review, and maintain documentation for product approvals and certifications from BIS (Bureau of Indian Standards), AERB (Atomic Energy Regulatory Board), and NABL (National Accreditation Board for Testing and Calibration Laboratories).
• Ensure all technical files, QA test reports , and compliance certificates are updated and aligned with current regulatory norms.
• Coordinate the submission and follow-up of applications for new product registrations, renewals, and amendments.
• Track changes in regulatory requirements and ensure timely updates to internal documentation and procedures.

2. Product and Process Compliance

• Ensure that manufacturing, testing, and quality processes for X-Ray, C-Arm, DR, and CT system assemblies comply with applicable regulatory standards.
• Collaborate with cross-functional teams to maintain compliance with ISO 13485, BIS 13450, and IEC 60601, QA Test & ISO 17025 series standards.
• Support internal reviews and audits to ensure readiness for inspections by AERB, BIS, or NABL authorities.
• Assist in preparing Technical Construction Files (TCF) and Declaration of Conformity (DoC) documents.

3. Coordination with Regulatory Authorities

• Liaise with regulatory bodies, certification agencies, and notified laboratories for product registration, testing, and approval activities.
• Ensure all correspondence with government or certification agencies is timely, accurate, and professionally maintained.
• Coordinate with testing laboratories for evaluation and compliance verification of imaging devices.

4. Documentation Control and Audits

• Manage regulatory documentation databases and ensure document traceability, version control, and secure archiving.
• Support internal and external audits related to regulatory compliance, ISO 13485, and GMP.
• Maintain audit readiness and participate in inspections by regulatory authorities.
• Prepare and circulate periodic compliance status reports to management.

5. Cross-Functional Support

• Collaborate with Design, Quality, Production, and Radiation Safety teams to ensure all regulatory requirements are met during product design, manufacturing, and testing.
• Support the preparation of technical dossiers, validation reports, and test summaries for regulatory submissions.
• Provide training and guidance to team members on regulatory documentation and compliance updates.

Qualifications and Experience:

• B.E. / B.Tech/Diploma in Electronics or Biomedical Engineering.
• 3-5 years (or more) of experience in Regulatory Affairs, Documentation, or Compliance within a medical device or imaging equipment manufacturing environment.
• Strong understanding of BIS, AERB, NABL, ISO 13485, GMP, and IEC 60601 standards.
• Experience with X-Ray, C-Arm, DR, and CT systems documentation and RS-QADXE compliance will be preferred.

Skills and Competencies:

• Excellent understanding of regulatory frameworks and documentation protocols for medical devices.
• Strong attention to detail and accuracy in documentation and data management.
• Good coordination and communication skills for interaction with authorities and internal teams.
• Proficient in MS Office, ERP, and document control systems.
• Strong analytical, organizational, and follow-up skills.
• Ability to interpret technical and regulatory guidelines effectively.

Key Performance Indicators (KPIs):

• Timely submission and renewal of regulatory licenses and certifications
• 100% compliance with BIS, AERB, and NABL requirements
• Accuracy and completeness of regulatory documentation
• Successful audit outcomes with minimal observations
• Effective coordination with authorities and testing agencies

India Radiology Alliances & BD Lead

AMRIscan India | Preventive Radiology | MRI | Diagnostic Center Network

Location: India / Remote

Type: Founding team

Compensation: Equity-led + performance-linked upside initially

Company: AMRIscan

Sector: Preventive Radiology | MRI | Teleradiology | Longevity Health | HealthTech

AMRIscan is looking for a radiology entrepreneur / healthcare business builder who wants to help build a preventive radiology platform of an US based company in India from the ground up. It is for someone who understands the radiology / diagnostic imaging ecosystem and wants to help create something meaningful, scalable, and early.

Please note that this opportunity is for some who likes building start ups and new businesses and is not meant for someone looking only for a salaried role, a routine consulting assignment, or a short-term project.

About AMRIscan:

AMRIscan is a U.S.-based preventive radiology startup building a next-generation platform focused on advanced MRI-based health insights, whole-body MRI, longevity reporting, and scalable imaging-center partnerships.

Our model is asset-light and partnership-driven. We work with radiologists, reporting groups, MRI-capable diagnostic centers, and healthcare operators to create a clinically governed preventive imaging ecosystem. AMRIscan is now set

Hiring for Radiology Coder| Certified Medical Coders | Noida

We are hiring experienced and detail-oriented Radiology Coders to join our growing healthcare team.

Position:

Radiology Senior Medical Coder

Job Location: Delhi NCR Noida

Experience Required:

2-5 Years in Medical Coding (Radiology Specialty Preferred)

Job Responsibilities:

• Review and assign accurate medical codes for radiology procedures and diagnoses.
• Ensure coding compliance with ICD-10, CPT, and HCPCS guidelines.
• Analyze radiology reports and medical records for proper documentation.
• Maintain coding accuracy and productivity standards.
• Work closely with QA and audit teams to resolve coding discrepancies.
• Stay updated with latest coding regulations and healthcare guidelines.
• Ensure confidentiality and compliance with HIPAA regulations.

Required Skills:

• Good knowledge of Radiology Coding.
• Strong understanding of ICD-10, CPT, and HCPCS coding systems.
• Familiarity with medical terminology, anatomy, and physiology.
• Good analytical and communication skills.
• Ability to maintain accuracy with productivity.

Eligibility Criteria:

• Certified Coders preferred (CPC/CCS/CIC).
• Immediate joiners preferred.

Job Title:

RA & QA Engineer – Regulatory & Safety (Radiology & Imaging Systems)

Department:

Regulatory & Safety – Radiology Division

Location:

Vapi, Gujarat

Reports To:

Manager / Senior Manager.

Job Purpose:

To manage and coordinate regulatory documentation and compliance activities for radiology and imaging systems such as X-Ray, C-Arm, Digital Radiography (DR), and CT equipment , ensuring adherence to BIS, AERB, NABL , and international regulatory standards applicable to medical device manufacturing.

Key Responsibilities:

1. Regulatory Documentation and Compliance

• Prepare, review, and maintain documentation for product approvals and certifications from BIS (Bureau of Indian Standards), AERB (Atomic Energy Regulatory Board), and NABL (National Accreditation Board for Testing and Calibration Laboratories).
• Ensure all technical files, QA test reports , and compliance certificates are updated and aligned with current regulatory norms.
• Coordinate the submission and follow-up of applications for new product registrations, renewals, and amendments.
• Track changes in regulatory requirements and ensure timely updates to internal documentation and procedures.

2. Product and Process Compliance

• Ensur

We are seeking a meticulous and proactive Radiology Prior Authorization Specialist to oversee and streamline the prior authorization (PA) process for radiology procedures. This role ensures timely and accurate approvals, reduces patient wait times, and supports compliance with payer requirements.

You will collaborate with radiologists, technologists, billing staff, and insurance providers to facilitate access to essential diagnostic and therapeutic radiology services.

Responsibilities

• Manage Prior Authorization Process: Handle the full lifecycle of prior authorizations for radiology procedures and imaging services (e.g., MRI, CT, PET, Ultrasound).
• Review Requests: Assess prior authorization submissions for completeness, ensuring alignment with medical necessity and payer guidelines.
• Team Collaboration: Work with radiologists, imaging departments, and billing teams to collect and submit accurate clinical documentation.
• Insurance Coordination: Communicate with insurance carriers to resolve denials,manage appeals, and minimize barriers to timely care.
• Maintain Records: Keep detail edand compliant records of all authorizations, including statuses and correspondence.
• Problem Resolution: Identify issues early in the process and implement solutions to accelerate authorization turnaround times.
• Stay Current: Monitor up