Qureos Mentor

Meril

<div>
 
 🌍 Join Meril Life Sciences &ndash; Driving India&rsquo;s Healthcare Revolution!
 
 
 
 
 
 Meril Life Sciences is a global Indian medical device company transforming lives through innovation. With a presence in 150+ countries and a strong team of 14,000+ professionals, we design, manufacture, and deliver cutting-edge solutions in *cardiology, orthopedics, and beyond* &mdash; all driven by research and a mission to make healthcare better for everyone.
 
 
 
 
 
 🚀 We Are Growing in Rajasthan &mdash; Explore Your Next Career Move!
 
 
 
 
 
 We are onboarding passionate sales professionals to join our district-level field team in Rajasthan.
 
 
 
 
 
 🔹 Open Opportunities (District Vacancies):
 
 
 &bull; Jaipur, Barmer, Chittorgarh, Nagaur, Dholpur and Tonk
 
 
 
 
 
 👤 You&rsquo;re a great fit if you have:
 
 
 ✅ 4&ndash;5 years of experience in Medical Devices / Surgical / Pharma Sales
 
 
 ✅ Strong relationship-building &amp; territory management skills
 
 
 ✅ Local candidates with a consistent career track record
 
 
 
 
 
 💼 CTC Range: ₹ Upto 6 LPA
 
 
 
 
 
 📩 Ready to grow with us?
 
 
 Send your CV at: recruit.sb@merillife.com
 
 
 💡 Subject Line: Application for DAM &ndash; District Name &ndash; Rajasthan
 
 
 
 
 
 ✨ Meril Life Sciences &mdash; Where Innovation Meets Impact.
 
 
 Be part of an organization where every sale contributes to improving healthcare outcomes across India &mdash; and where our innovations touch lives around the world.
 
</div>

District Associate Manager

<div>
 
 
 Job Title:
 
 
 
 
 Regulatory Affairs Executive &ndash; Regulatory &amp; Safety (Radiology &amp; Imaging Systems)
 
 
 
 
 Department:
 
 
 
 Regulatory &amp; Safety &ndash; Radiology Division
 
 
 
 Location:
 
 
 
 Vapi, Gujarat
 
 
 
 Reports To:
 
 
 
 Manager / Senior Manager &ndash; Regulatory &amp; 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
 
 
 <ul>
 <li>
 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).
 
 </li>
 <li>
 Ensure all technical files, QA test reports , and compliance certificates are updated and aligned with current regulatory norms.
 </li>
 <li>
 Coordinate the submission and follow-up of applications for new product registrations, renewals, and amendments.
 </li>
 <li>
 Track changes in regulatory requirements and ensure timely updates to internal documentation and procedures.
 </li>
 </ul>
 
 
 2. Product and Process Compliance
 
 
 <ul>
 <li>
 Ensure that manufacturing, testing, and quality processes for
 
 X-Ray, C-Arm, DR, and CT system assemblies
 
 comply with applicable regulatory standards.
 </li>
 <li>
 Collaborate with cross-functional teams to maintain compliance with
 
 ISO 13485, BIS 13450, and IEC 60601, QA Test &amp; ISO 17025
 
 series standards.
 </li>
 <li>
 Support internal reviews and audits to ensure readiness for inspections by
 
 AERB, BIS, or NABL
 
 authorities.
 </li>
 <li>
 Assist in preparing
 
 Technical Construction Files (TCF)
 
 and
 
 Declaration of Conformity (DoC)
 
 documents.
 </li>
 </ul>
 
 
 3. Coordination with Regulatory Authorities
 
 
 <ul>
 <li>
 Liaise with
 
 regulatory bodies, certification agencies, and notified laboratories
 
 for product registration, testing, and approval activities.
 </li>
 <li>
 Ensure all correspondence with government or certification agencies is timely, accurate, and professionally maintained.
 </li>
 <li>
 Coordinate with
 
 testing laboratories
 
 for evaluation and compliance verification of imaging devices.
 </li>
 </ul>
 
 
 4. Documentation Control and Audits
 
 
 <ul>
 <li>
 Manage regulatory documentation databases and ensure document traceability, version control, and secure archiving.
 </li>
 <li>
 Support internal and external audits related to
 
 regulatory compliance, ISO 13485, and GMP.
 
 </li>
 <li>
 Maintain audit readiness and participate in inspections by regulatory authorities.
 </li>
 <li>
 Prepare and circulate periodic compliance status reports to management.
 </li>
 </ul>
 
 
 5. Cross-Functional Support
 
 
 <ul>
 <li>
 Collaborate with
 
 Design, Quality, Production, and Radiation Safety
 
 teams to ensure all regulatory requirements are met during product design, manufacturing, and testing.
 </li>
 <li>
 Support the preparation of technical dossiers, validation reports, and test summaries for regulatory submissions.
 </li>
 <li>
 Provide training and guidance to team members on regulatory documentation and compliance updates.
 </li>
 </ul>
 
 
 
 
 
 Qualifications and Experience:
 
 
 <ul>
 <li>
 
 B.E. / B.Tech/Diploma in Electronics or Biomedical Engineering
 
 .
 </li>
 <li>
 
 3&ndash;5 years (or more)
 
 of experience in
 
 Regulatory Affairs, Documentation, or Compliance
 
 within a
 
 medical device or imaging equipment manufacturing
 
 environment.
 </li>
 <li>
 Strong understanding of
 
 BIS, AERB, NABL, ISO 13485, GMP, and IEC 60601
 
 standards.
 </li>
 <li>
 Experience with
 
 X-Ray, C-Arm, DR, and CT systems
 
 documentation and RS-QADXE compliance will be preferred.
 </li>
 </ul>
 
 
 
 
 
 Skills and Competencies:
 
 
 <ul>
 <li>
 Excellent understanding of
 
 regulatory frameworks and documentation protocols
 
 for medical devices.
 </li>
 <li>
 Strong attention to detail and accuracy in documentation and data management.
 </li>
 <li>
 Good coordination and communication skills for interaction with authorities and internal teams.
 </li>
 <li>
 Proficient in
 
 MS Office, ERP, and document control systems.
 
 </li>
 <li>
 Strong analytical, organizational, and follow-up skills.
 </li>
 <li>
 Ability to interpret technical and regulatory guidelines effectively.
 </li>
 </ul>
 
 
 
 
 
 Key Performance Indicators (KPIs):
 
 
 <ul>
 <li>
 Timely submission and renewal of regulatory licenses and certifications
 </li>
 <li>
 100% compliance with BIS, AERB, and NABL requirements
 </li>
 <li>
 Accuracy and completeness of regulatory documentation
 </li>
 <li>
 Successful audit outcomes with minimal observations
 </li>
 <li>
 Effective coordination with authorities and testing agencies
 </li>
 </ul>
</div>

Regulatory Affairs Executive - Radiology

<div>
 
 
 Job Title:
 
 
 
 
 Assistant Product Manager &ndash; International Marketing
 
 
 
 
 Business Unit:
 
 Meril Endo-Surgery
 
 
 
 Location:
 
 Mumbai
 
 
 
 Reports To:
 
 Deputy General Manager
 
 
 
 
 
 
 Role Overview:
 
 
 
 The Assistant Product Manager &ndash; International Marketing will support the global growth and brand positioning of Meril Endo-Surgery. This role involves surgeon engagement, product launches, medical education initiatives, marketing collateral development, campaign execution, and cross-functional collaboration to enhance the company's international footprint.
 
 
 
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Represent Meril at international congresses and share actionable market insights.
 </li>
 <li>
 Drive surgeon engagement through summits, observerships, workshops and training programs.
 </li>
 <li>
 Support international product launches and track market adoption.
 </li>
 <li>
 Design marketing materials such as brochures, catalogues, sales aids, gifts, and brand reminders.
 </li>
 <li>
 Develop teaser videos, animations, and visual content in collaboration with creative teams.
 </li>
 <li>
 Plan and execute digital campaigns with the digital marketing team.
 </li>
 <li>
 Collaborate with vendors and cross-functional teams including R&amp;D, Clinical, Regulatory, Finance, Supply chain and Sales for strategic alignment.
 </li>
 </ul>
 
 
 
 
 
 Minimum Qualifications:
 
 
 <ul>
 <li>
 MBA (Marketing or related field) is mandatory.
 </li>
 <li>
 2&ndash;3 years of experience in marketing or 5&ndash;6 years of relevant sales experience in endo-mechanical.
 </li>
 <li>
 Strong communication, project management, and creative execution skills.
 </li>
 <li>
 Ability to work in a fast-paced, cross-functional, and global environment.
 </li>
 </ul>
 
 
</div>

Assistant Product Manager

<div>
 <ol>
 <li>
 Ensure the receipt, storage, dispatch and daily management of the stock items.
 </li>
 <li>
 Ensure the conformity of products received and delivered.
 </li>
 <li>
 Ensure the management of inventories: control of the rotation of goods, verification of their availability, procurement from suppliers, cleaning, inventory.
 </li>
 <li>
 Replenish supply inventories following established guidelines.
 </li>
 <li>
 check inventory records for accuracy
 </li>
 <li>
 keep records of items shipped, received, or transferred to another location
 </li>
 <li>
 compile reports on various aspects of changes in production or inventory.
 </li>
 <li>
 post details of receipt and dispatch transactions and ensure integrity of the inventory management system.
 </li>
 <li>
 provide information on current stock.
 </li>
 <li>
 Conduct periodic inventory stock counting inventory accuracy check.
 </li>
 <li>
 Preparation and amendment of new or existing SOP, EOP.
 </li>
 </ol>
 
 
</div>

Warehouse Specialist

<div>
 <ol>
 <li>
 Ensuring adherence to global trade compliance standards and staying updated on international regulations.
 </li>
 <li>
 Managing all documentation related to shipments, including invoices, bills of lading, and customs declarations.
 </li>
 <li>
 Monitoring and tracking shipments to ensure timely and efficient delivery.
 </li>
 <li>
 Ensuring compliance with import/export laws, regulations, and policies.
 </li>
 <li>
 Timely filing of bill of entry.
 </li>
 <li>
 Making sure all necessary documents are available at the time of delivery such as but not limited to Commercial invoice, Bill of entry, packing list , E-way bill etc
 </li>
 <li>
 Make sure all necessary import licenses, IEC are valid.
 </li>
 <li>
 Make sure licenses for duty benefits are available such As but not limited to DEEC/DEPB/ECGC etc..
 </li>
 <li>
 Filing of all required documents to get the materials cleared
 </li>
 <li>
 Arranging documents needed to clear vendor payments and getting necessary benefits of import and export.
 </li>
 </ol>
 
 Verifying vendor bills before payment release.
 
</div>

Supply Chain Manager

<div>
 
 
 Job Title: Full stack Developer
 
 
 
 
 Experience: 0 &ndash; 3 Years
 
 
 
 
 Location: Kanpur (New Technopark @ IIT Kanpur)
 
 
 
 
 Job Type: Full-Time
 
 
 
 
 
 
 Key Responsibilities:
 
 
 
 &middot; Design, develop, and maintain full-stack applications using MERN stack + PostgreSQL.
 
 
 &middot; Build and integrate RESTful APIs for seamless communication between front-end and back-end services.
 
 
 &middot; Develop responsive, interactive, and user-friendly front-end applications with React.js (JavaScript/TypeScript).
 
 
 &middot; Write clean, modular, and maintainable code following industry best practices.
 
 
 &middot; Ensure security, scalability, and high performance of applications in production.
 
 
 &middot; Troubleshoot, debug, and optimize system performance.
 
 
 &middot; Participate in code reviews, documentation, and knowledge sharing.
 
 
 
 
 
 Required Skills:
 
 
 
 &middot; 0&ndash;3 years of professional experience in full-stack development.
 
 
 &middot; Strong expertise in MERN stack (MongoDB, Express.js, React.js, Node.js).
 
 
 &middot; Proficiency in JavaScript/TypeScript for front-end and back-end.
 
 
 &middot; Knowledge of authentication and authorization mechanisms (JWT, OAuth2).
 
 
 &middot; Good understanding of complete SDLC.
 
 
 
 
 
 Preferred / Additional Skills:
 
 
 
 &middot; Experience with testing frameworks (Vitest, Mocha, Cypress, PyTest).
 
 
 &middot; Strong awareness of security best practices, performance tuning, and optimization.
 
 
 &middot; Practical experience with Docker.
 
 
 
 
 
 Employment Bond:
 
 
 <ul>
 <li>
 1 Years
 </li>
 </ul>
 
 
</div>

Full Stack Engineer

<div>
 
 
 Job Title:
 
 
 
 
 QC Testing Engineer &ndash; Radiology &amp; Imaging Systems (X-Ray / C-Arm / DR / CT)
 
 
 
 
 Department:
 
 
 
 Quality Control / Quality Assurance &ndash; Radiology Division
 
 
 
 Location:
 
 
 
 Vapi, Gujarat
 
 
 
 Reports To:
 
 
 
 QC Supervisor / Manager &ndash; Radiology Systems
 
 
 
 
 
 
 Job Purpose:
 
 
 
 To perform quality control testing, inspection, and validation of
 
 radiology and imaging systems
 
 including
 
 X-Ray, C-Arm, Digital Radiography (DR), and CT Scan equipment
 
 , ensuring compliance with
 
 BIS, ISO, and IEC standards
 
 and maintaining the highest levels of safety, accuracy, and reliability.
 
 
 
 
 
 
 Key Responsibilities:
 
 
 
 
 1. Product Testing and Inspection
 
 
 <ul>
 <li>
 Conduct
 
 electrical, mechanical, radiation, and functional testing
 
 of X-Ray, C-Arm, DR, and CT systems as per approved test procedures and standards.
 </li>
 <li>
 Verify system performance parameters including
 
 radiation output, image quality, electrical safety, mechanical stability, and operational accuracy.
 
 </li>
 <li>
 Carry out
 
 pre-dispatch inspection (PDI)
 
 and
 
 final acceptance testing
 
 before equipment release.
 </li>
 <li>
 Ensure complete adherence to
 
 BIS 13450
 
 ,
 
 ISO 13485
 
 , and
 
 IEC 60601
 
 series standards for medical electrical and imaging equipment.
 </li>
 </ul>
 
 
 2. Quality Compliance and Documentation
 
 
 <ul>
 <li>
 Maintain detailed and accurate
 
 testing records, calibration data, and inspection reports
 
 in line with internal and external audit requirements.
 </li>
 <li>
 Ensure strict compliance with
 
 Good Manufacturing Practices (GMP)
 
 and quality management documentation.
 </li>
 <li>
 Identify non-conformities, assist in
 
 root cause analysis
 
 , and implement
 
 Corrective and Preventive Actions (CAPA).
 
 </li>
 <li>
 Collaborate with R&amp;D, Production, and QA teams to continuously improve product quality and testing efficiency.
 </li>
 </ul>
 
 
 3. Equipment Calibration and Maintenance
 
 
 <ul>
 <li>
 Ensure all testing and measuring instruments are
 
 calibrated, certified, and properly maintained
 
 .
 </li>
 <li>
 Perform or support calibration of
 
 radiation meters, electrical safety analyzers, imaging test phantoms, and mechanical gauges.
 
 </li>
 <li>
 Monitor and maintain environmental, radiation, and electrical safety standards during testing operations.
 </li>
 </ul>
 
 
 4. Standards and Regulatory Alignment
 
 
 <ul>
 <li>
 Execute testing as per
 
 BIS, ISO 13485, IEC 60601
 
 , and related
 
 medical imaging equipment standards.
 
 </li>
 <li>
 Stay updated with new and revised standards for diagnostic imaging systems including DR, X-Ray, and CT equipment.
 </li>
 <li>
 Participate in internal and external audits by certification and regulatory authorities.
 </li>
 </ul>
 
 
 
 
 
 Qualifications and Experience:
 
 
 <ul>
 <li>
 
 B.E. / B.Tech / Diploma
 
 in
 
 Electronics, Biomedical.
 
 </li>
 <li>
 
 3&ndash;5 years (or more)
 
 of experience in
 
 Quality Control, Testing, or Validation
 
 of radiology or medical imaging equipment.
 </li>
 <li>
 Hands-on experience in testing
 
 X-Ray generators, DR detectors, high-voltage assemblies, and imaging control systems.
 
 </li>
 <li>
 Strong knowledge of
 
 BIS, ISO 13485, GMP, and IEC 60601
 
 compliance requirements for medical devices.
 </li>
 </ul>
 
 
 
 
 
 Skills and Competencies:
 
 
 <ul>
 <li>
 Proficiency in using
 
 radiation dosimeters, electrical safety analyzers, image quality test phantoms, and calibration tools.
 
 </li>
 <li>
 Strong analytical and diagnostic skills with attention to detail.
 </li>
 <li>
 Excellent documentation, observation, and reporting capabilities.
 </li>
 <li>
 Familiarity with
 
 high-voltage systems, digital imaging detectors, and DICOM standards
 
 preferred.
 </li>
 <li>
 Good communication, teamwork, and cross-functional coordination skills.
 </li>
 <li>
 Commitment to quality, safety, and continuous improvement.
 </li>
 </ul>
 
 
 
 
 
 Key Performance Indicators (KPIs):
 
 
 <ul>
 <li>
 Accuracy and completeness of test reports
 </li>
 <li>
 Compliance with BIS / ISO / IEC standards
 </li>
 <li>
 Reduction in product rejections and field complaints
 </li>
 <li>
 Timely completion of testing activities
 </li>
 <li>
 Successful audit outcomes and documentation readiness
 </li>
 </ul>
 
 
</div>

QC Testing Engineer - X-Ray / C-Arm / DR / CT

Join Meril and explore 7   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.