Talent.com
Regulatory Affairs Executive - Radiology

Regulatory Affairs Executive - Radiology

Merilnagpur, India
1 day ago
Job description

Job Title :

Regulatory Affairs Executive – Regulatory & Safety (Radiology & Imaging Systems)

Department :

Regulatory & Safety – Radiology Division

Location : Vapi, Gujarat

Reports To :

Manager / Senior Manager – Regulatory & Safety

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
  • Create a job alert for this search

    Executive Regulatory • nagpur, India

    Related jobs
    • Promoted
    Regional Sales Executive (Government Sector) – (India)

    Regional Sales Executive (Government Sector) – (India)

    NOTHREATnagpur, maharashtra, in
    Nothreat is a rapidly growing cybersecurity startup recognized by leading global accelerators, including the Google AI Startup Program, Grow London (7th Cohort Accelerator), and the CMS equIP Globa...Show moreLast updated: 1 day ago
    • Promoted
    Regulatory Affairs Associate I

    Regulatory Affairs Associate I

    Teva Pharmaceuticalsnagpur, India
    Regulatory Affairs Associate I (Regulatory Operation- Regulatory Data Analytics).The role of GRO Regulatory Data Analytics is to : . Manage Teva’s data in accordance with requirements for xEVPMD in or...Show moreLast updated: 16 days ago
    • Promoted
    • New!
    Senior Executive

    Senior Executive

    SCHOTT Poonawallanagpur, maharashtra, in
    This role will be responsible for implementing and maintaining Environment, Health, and Safety systems and ensuring compliance with statutory, corporate, and site-specific EHS requirements.The role...Show moreLast updated: 11 hours ago
    • Promoted
    Product Executive – DMC

    Product Executive – DMC

    Anyfly DmcNagpur, IN
    We specialize in destinations such as.This role requires a deep understanding of destination knowledge, cost management, and itinerary planning. Handle all B2B queries and provide accurate quotation...Show moreLast updated: 23 days ago
    • Promoted
    Senior Medical Safety Advisor

    Senior Medical Safety Advisor

    IQVIANagpur, IN
    Pharmacovigilance / PV Experience.The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance pr...Show moreLast updated: 30+ days ago
    • Promoted
    Senior Regulatory Affairs Trainer(Medical Devices)

    Senior Regulatory Affairs Trainer(Medical Devices)

    Tek Supportnagpur, maharashtra, in
    Job Title : Senior Trainer – Regulatory Affairs (Medical Devices).The ideal candidate will have hands-on experience in global regulatory submissions, product registration, quality system compliance,...Show moreLast updated: 1 day ago
    • Promoted
    • New!
    Regulatory Affairs Specialist

    Regulatory Affairs Specialist

    Zydus MedTechIndia
    To lead regulatory submissions and compliance activities for cardiovascular medical devices, specifically drug‑eluting stents, balloon catheters, and related vascular devices.Ensure adherence to In...Show moreLast updated: 13 hours ago
    • Promoted
    Executive - Regulatory Affairs

    Executive - Regulatory Affairs

    ConfidentialIndia
    Executive – Regulatory & Business Continuity.At Sun Pharma, we commit to helping you 'Create your own sunshine'— by fostering an environment where you grow at every step, take charge of your journe...Show moreLast updated: 5 days ago
    • Promoted
    Regulatory Affairs Associate

    Regulatory Affairs Associate

    SAIN MEDICAMENTS PVT. LTDRepublic Of India, IN
    Sain Medicaments Pvt Ltd – Hyderabad.Sain Medicaments Pvt Ltd is a leading pharmaceutical formulation company, proudly serving Human healthcare since 1970s, we have come a long way to make a mark i...Show moreLast updated: 1 day ago
    • Promoted
    Senior Associate, Pharma Commercial Operations

    Senior Associate, Pharma Commercial Operations

    KMK Consulting Inc.Nagpur, IN
    KMK is a global data analytics and technology consulting company empowering leaders across the Life Sciences industries to make better data-driven decisions. Our data analytics and software platform...Show moreLast updated: 30+ days ago
    • Promoted
    Radiologist

    Radiologist

    Wockhardt Hospitals Nagpurnagpur, maharashtra, in
    This is a full-time on-site role for a Radiologist at Wockhardt Hospitals in Nagpur.The Radiologist will be responsible for diagnosing and treating illnesses using medical imaging techniques includ...Show moreLast updated: 1 day ago
    • Promoted
    Radiology Medical Coder

    Radiology Medical Coder

    Talentgigsnagpur, maharashtra, in
    Job Title : Radiology QA Specialist.The Radiology QA Specialist ensures accuracy, quality, and compliance of radiology coding,. This role reviews audits, identifies errors or trends, and works.Audit ...Show moreLast updated: 30+ days ago
    • Promoted
    Oncology Prior Authorisation

    Oncology Prior Authorisation

    Taglynknagpur, maharashtra, in
    As a CoverMyMeds Specialist, you will be responsible for managing electronic prior authorizations (ePAs) and ensuring timely and accurate processing of oncology-related prescriptions.You will work ...Show moreLast updated: 30+ days ago
    • Promoted
    Regulatory Affairs Manager

    Regulatory Affairs Manager

    Chemill Pharma Ltd.Republic Of India, IN
    Chemill Pharma is seeking a seasoned and detail-oriented Regulatory Affairs Manager to lead and oversee all regulatory activities across ASEAN markets and Hong Kong, while providing regional suppor...Show moreLast updated: 1 day ago
    • Promoted
    Radiation Safety Executive

    Radiation Safety Executive

    MerilIndia
    Radiation Safety Executive – Regulatory & Safety (Radiology & Imaging Systems).Regulatory & Safety – Radiology Division.Manager / Senior Manager – Regulatory & Safety. To ensure radiation safety, re...Show moreLast updated: 1 day ago
    • Promoted
    Maritime Regulatory Manager - Based in UK

    Maritime Regulatory Manager - Based in UK

    Comaea ConsultingNagpur, IN
    Our client is a MNC n the maritime industry.To support the growth strategy and its expansion, our client is seeking an experienced. We are hiring on behalf of a leading global shipowner and shipping...Show moreLast updated: 1 day ago
    • Promoted
    • New!
    Regulatory Affairs Specialist – (APAC & RoW)

    Regulatory Affairs Specialist – (APAC & RoW)

    vueverse.Nagpur, IN
    Regulatory Submissions & Compliance.Author, compile, and submit regulatory dossiers to global health authorities, including USFDA, EMA, MHRA, TGA, HSA, NPRA, Thai FDA, Taiwan FDA, CDE, NMPA, PMDA, ...Show moreLast updated: 15 hours ago
    • Promoted
    • New!
    Senior Executive Talent Acquisition

    Senior Executive Talent Acquisition

    Vista Consoles Electronics Private Limitednagpur, maharashtra, in
    Take care of complete lifecycle of recruitment processes.Finding suitable CVs from Job Portals, social medial and other resources is major KRA. Compensation and benefits benchmarking systems that fi...Show moreLast updated: 11 hours ago