The medical device sector in India presents significant career opportunities for professionals with diverse skill sets. Job seekers can find roles spanning research and development, manufacturing, quality assurance, regulatory affairs, sales, and marketing. These positions require a strong understanding of medical technology, healthcare regulations, and market dynamics.8 Medical Device jobs in India
Plant Head - Medical Device
Posted 5 days ago
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Job Description
Job Summary:
The Plant Head will be responsible for overall management, planning, and control of plant operations — ensuring optimum utilization of manpower, materials, and machinery while maintaining the highest standards of productivity, quality, safety, and regulatory compliance (ISO 13485, CE, MDR, GMP).
This role requires a strong leader who can align cross-functional teams (Production, QA, QC, Maintenance, Purchase, Stores, HR, ) toward achieving company goals in efficiency, cost control, and on-time delivery , while driving a culture of continuous improvement.
Key Responsibilities:1. Strategic Planning & Operations Control
- Lead day-to-day plant operations to achieve monthly and annual production targets.
- Develop and implement production plans based on demand forecasts and export schedules.
- Monitor KPIs for OEE, productivity, yield, downtime, rejection, and delivery performance.
- Optimize production planning, batch scheduling, and resource allocation to minimize bottlenecks.
2. Quality, Regulatory & Compliance
- Ensure strict adherence to ISO 13485:2016, CE, MDR, and GMP standards across all processes.
- Collaborate with QA and QC to maintain product quality, conduct internal audits, and resolve non-conformities.
- Maintain full traceability and documentation for batch manufacturing, sterilization, and packaging.
- Support internal and external audits (MOH, clients, notified bodies).
3. Team Leadership & Development
- Lead a multidisciplinary team across Production, QA/QC, Maintenance, Purchase, Store, and HR .
- Define departmental KPIs and conduct regular performance reviews.
- Train and motivate employees to ensure accountability, productivity, and safety compliance.
- Foster a culture of teamwork, discipline, and continuous learning.
4. Cost & Efficiency Management
- Monitor manufacturing costs, wastage, and material utilisation to improve profit margins.
- Implement Lean Manufacturing, Kaizen, and 5S principles for continuous improvement.
- Review cost sheets, BOM accuracy, and process efficiency for cost optimisation.
5. Maintenance & Facility Management
- Oversee preventive and breakdown maintenance of machinery, utilities, AHUs, and ETO sterilisation units.
- Ensure uninterrupted production through effective maintenance planning.
- Coordinate for calibration, validation, and facility upkeep as per GMP norms.
6. Production Documentation & Traceability
- Ensure timely Flow of BMR (Batch Manufacturing Record), BPR (Batch Packaging Record) , and other production documents.
- Maintain full traceability from raw material to dispatch.
- Coordinate with QA for change control, deviation, CAPA, and process validation.
7. Safety, Environment & Compliance
- Ensure implementation of EHS (Environment, Health & Safety) standards.
- Conduct regular safety drills, equipment audits, and compliance checks.
- Maintain hygienic and controlled manufacturing environments as per cleanroom classifications.
8. Cross-Functional Coordination
- Collaborate with Purchase, Sales, Planning, and Finance to ensure smooth operations.
- Review production vs. dispatch schedules and support on-time shipment for export orders.
- Participate in management review meetings and strategic business planning.
Key Skills & Competencies:
- Strong leadership, communication, and analytical abilities.
- In-depth understanding of medical device manufacturing processes (injection molding, assembly, ETO sterilization, packaging).
- Familiar with ISO 13485 documentation, CE marking, and GMP systems.
- Sound knowledge of production planning, maintenance, inventory, and manpower management.
- Proficiency in MS Office / ERP systems.
- Decision-making and problem-solving mindset.
Qualification & Experience:
- Bachelor’s / Master’s degree in Engineering, Industrial Management, or Production.
- Minimum 5-10 years of experience in manufacturing, with at least 2 years in a senior leadership role (preferably in medical devices, pharma, or cleanroom manufacturing ).
- Hands-on experience with ISO 13485 audits, ETO sterilization, and CE compliance preferred.
Medical Device Sales Representative
Posted 5 days ago
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Job Description
Job Opportunity – Cardiac Division |
Leading Medical Devices Company -
Are you working in the Cardiac Devices or Cardiac Pharma space and looking for your next big opportunity?
Join a leading Medical Devices company focused on Cardiac Stents & Balloons as part of our expanding Cardiac Division
Who Can Apply:
️ Candidates currently working on Dealer/Distributor payroll handling Cardiac Stents, Balloons, etc.
️ Professionals from Pharma companies handling only Cardiac Portfolio as:
Therapy Managers
Key Account Managers
Medical Representatives
What We’re Looking For:
Strong technical knowledge of cardiac therapies
Excellent communication skills
1–2 years of experience in the cardiac segment (mandatory for pharma background)
CTC - Depends upon the interview
Senior Security Engineer - Medical Device Cybersecurity & Compliance
Posted 2 days ago
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Senior Security Engineer - Medical Device Cybersecurity & Compliance
**Job Description:**
Job Description
**Job Title: Senior Security Engineer - Medical Device Cybersecurity & Compliance**
**Experience Level: 5-10 years**
**Key Responsibilities:**
+ Drive end-to-end cybersecurity integration across the medical device product development life cycle, ensuring security is embedded from concept to release.
+ Develop and maintain cybersecurity for medical products, including security requirements specifications, risk assessments, threat models, and product security architecture documentation.
+ Conduct thorough gap assessments to evaluate compliance with IEC 81001-5-1, IEC 60601-4-5, AAMI TIR 57, and AAMI TIR 97 standards, and implement remediation measures.
+ Perform hands-on vulnerability assessments, penetration testing, and secure code reviews of embedded devices, IoMT (Internet of Medical Things) components, and connected systems.
+ Collaborate closely with development, compliance, and regulatory teams to ensure product security measures meet both internal security policies and external regulatory expectations.
+ Support SBOM management, software supply chain risk evaluations, and third-party component analysis to maintain software transparency and mitigate risks.
+ Provide expert input on secure communication protocols, encryption standards, data protection for both at-rest and in-transit data, and cloud-based connectivity of medical systems.
+ Assist in developing incident response strategies and bring working knowledge of HIPAA, GDPR, and HL7 to address data privacy and healthcare-specific regulatory concerns.
+ Contribute to the continuous enhancement of internal secure development processes, tools, and methodologies, while championing security best practices within product teams.
**Required Skills and Qualifications:**
+ Minimum of 6 years of experience in cybersecurity, including at least 3 years focused on medical devices, embedded systems, or IoT security.
+ Proven track record in authoring security design, defining technical requirements, and documenting security architectures aligned with regulatory needs.
+ Hands-on experience in embedded system security including secure boot, firmware security, threat modeling techniques (e.g., STRIDE, DREAD), and product-level risk assessments.
+ Strong understanding of IEC 81001-5-1, IEC 60601-4-5, AAMI TIR 57, and AAMI TIR 97, along with working knowledge of the medical device product development lifecycle and quality standards like ISO 14971.
+ Demonstrated expertise in vulnerability management and penetration testing of connected products across device and cloud ecosystems.
+ Familiarity with data privacy and interoperability standards such as HIPAA, GDPR, and HL7 is highly desirable.
+ Excellent problem-solving skills, critical thinking, and ability to lead gap analysis and remediation activities in regulated environments.
+ Strong collaboration skills with the ability to influence cross-functional teams including R&D, compliance, and product management.
**Location:**
IN-GJ-Ahmedabad, India-Ognaj (eInfochips)
**Time Type:**
Full time
**Job Category:**
Engineering Services
Arrow Electronics, Inc.'s policy is to provide equal employment opportunities to all qualified employees and applicants without regard to race, color, religion, age, sex, marital status, gender identity or expression, sexual orientation, national origin, disability, citizenship, veran status, genetic information, or any other characteristics protected by applicable state, federal or local laws. Our policy of equal employment opportunity and affirmative action applies to all employment decisions personnel policies and practices, or programs.
Senior Security Engineer - Medical Device Cybersecurity & Compliance
Posted 2 days ago
Job Viewed
Job Description
Senior Security Engineer - Medical Device Cybersecurity & Compliance
**Job Description:**
Job Description
**Job Title: Senior Security Engineer - Medical Device Cybersecurity & Compliance**
**Experience Level: 5-10 years**
**Key Responsibilities:**
+ Drive end-to-end cybersecurity integration across the medical device product development life cycle, ensuring security is embedded from concept to release.
+ Develop and maintain cybersecurity for medical products, including security requirements specifications, risk assessments, threat models, and product security architecture documentation.
+ Conduct thorough gap assessments to evaluate compliance with IEC 81001-5-1, IEC 60601-4-5, AAMI TIR 57, and AAMI TIR 97 standards, and implement remediation measures.
+ Perform hands-on vulnerability assessments, penetration testing, and secure code reviews of embedded devices, IoMT (Internet of Medical Things) components, and connected systems.
+ Collaborate closely with development, compliance, and regulatory teams to ensure product security measures meet both internal security policies and external regulatory expectations.
+ Support SBOM management, software supply chain risk evaluations, and third-party component analysis to maintain software transparency and mitigate risks.
+ Provide expert input on secure communication protocols, encryption standards, data protection for both at-rest and in-transit data, and cloud-based connectivity of medical systems.
+ Assist in developing incident response strategies and bring working knowledge of HIPAA, GDPR, and HL7 to address data privacy and healthcare-specific regulatory concerns.
+ Contribute to the continuous enhancement of internal secure development processes, tools, and methodologies, while championing security best practices within product teams.
**Required Skills and Qualifications:**
+ Minimum of 6 years of experience in cybersecurity, including at least 3 years focused on medical devices, embedded systems, or IoT security.
+ Proven track record in authoring security design, defining technical requirements, and documenting security architectures aligned with regulatory needs.
+ Hands-on experience in embedded system security including secure boot, firmware security, threat modeling techniques (e.g., STRIDE, DREAD), and product-level risk assessments.
+ Strong understanding of IEC 81001-5-1, IEC 60601-4-5, AAMI TIR 57, and AAMI TIR 97, along with working knowledge of the medical device product development lifecycle and quality standards like ISO 14971.
+ Demonstrated expertise in vulnerability management and penetration testing of connected products across device and cloud ecosystems.
+ Familiarity with data privacy and interoperability standards such as HIPAA, GDPR, and HL7 is highly desirable.
+ Excellent problem-solving skills, critical thinking, and ability to lead gap analysis and remediation activities in regulated environments.
+ Strong collaboration skills with the ability to influence cross-functional teams including R&D, compliance, and product management.
**Location:**
IN-GJ-Ahmedabad, India-Ognaj (eInfochips)
**Time Type:**
Full time
**Job Category:**
Engineering Services
Arrow Electronics, Inc.'s policy is to provide equal employment opportunities to all qualified employees and applicants without regard to race, color, religion, age, sex, marital status, gender identity or expression, sexual orientation, national origin, disability, citizenship, veran status, genetic information, or any other characteristics protected by applicable state, federal or local laws. Our policy of equal employment opportunity and affirmative action applies to all employment decisions personnel policies and practices, or programs.
Senior Manager/Manager - Projects - Medical Device Testing
Posted 5 days ago
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Job Description
Key Responsibilities:
- Experiences into testing and certification of Active Medical devices for various 60601 basic and product standards
- Knowledge on ISO 13485, ISO 14971, etc
- Responsible to handle the Active Medical Device business segment of EnE for complete Indian region
- Responsible to develop the business of Active medical devices and sustain the business
- Responsible to drive the challenging targets with Techno-commercial knowledge
- Should work closely with Laboratory team to develop test methods for Active Medical devices
- Should work closely with Sales and Marketing teams
- Responsible to build his strong team across India
- Having experience in handling P&L responsibilities
- Should possess high attributions in winning culture
- Having responsibilities in handling a team of 5-10 experts
- Should have a strong knowledge on Medical Device testing market in India
- Having in-depth knowledge of Active Medical equipment’s requirements for various countries
- Should have a strong command on Active medical device regulations for India & Global
- Should have a strong presentation, communication and interpersonal skills
Education & Work Experiences:
- Bachelor of Engineering or B.tech
- 12 - 15 Years of Work Experiences
Medical Equipment Service Manager
Posted 5 days ago
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Job Description
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This is a full-time on-site role for a Medical Equipment Service Manager located in Kolkata. The Medical Equipment Service Manager will be responsible for overseeing the maintenance and repair of medical equipment, ensuring that all equipment is functioning properly and meets regulatory standards. Additional day-to-day tasks include managing service contracts, coordinating with medical staff for equipment needs, and ensuring compliance with safety and accreditation standards. The role requires regular interaction with customers to resolve service issues and provide exceptional customer service.
- Credentialing, Medical Staff Credentialing, and Accreditation skills
- Knowledge of Medicine, medical equipment, and regulatory compliance
- Strong Customer Service skills
- Excellent problem-solving and organizational skills
- Ability to work independently and as part of a team
- Bachelor's degree in a relevant field such as biomedical engineering or healthcare management
- Prior experience in a similar role within the healthcare industry is a plus
Medical equipment sales manager
Posted 9 days ago
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Job Description
Company Overview
Job Hub Hr is a leading recruitment agency headquartered in Bangalore, specializing in staffing and recruitment services across India. Known for its expertise in connecting organizations with talented individuals, Job Hub Hr leverages intelligent technology to maximize human potential within the Human Resources Services industry. With a team size of 11-50 employees, the company is recognized for its passion and commitment to excellence in staffing and job consultancy services.
Job Overview
We are seeking a dynamic and experienced Medical Equipment Sales Manager for our client in Bangalore Urban. This is a full-time, mid-level position requiring a minimum of 4 to a maximum of 6 years of work experience. The ideal candidate will possess expertise in medical equipment and devices sales and demonstrate strong leadership and strategic sales skills to drive growth and success in the B2B sector.
Qualifications and Skills
- Proven experience in medical equipment sales, demonstrating successful track record. (Mandatory skill)
- Strong background in medical devices sales, showcasing ability to meet and exceed targets. (Mandatory skill)
- In-depth knowledge of medical devices, ensuring understanding of product range and market trends.
- Experience as a sales manager with a focus on leadership and team development.
- Expertise in B2B sales, capable of managing the sales process to business clients effectively.
- Proficient in sales strategy development and execution to achieve business objectives.
- Excellent communication and negotiation skills for building and maintaining client relationships.
- Strong analytical and problem-solving abilities to address sales challenges and opportunities.
Roles and Responsibilities
- Develop and implement strategic sales plans to expand the company's presence in the medical equipment sector.
- Lead and manage a team of sales professionals to achieve set sales targets and objectives.
- Build and maintain strong relationships with clients, offering personalized sales support and solutions.
- Identify and capitalize on new business opportunities within the medical equipment industry.
- Conduct market research to stay up-to-date with industry trends and competitive landscape.
- Collaborate with marketing teams to promote products and drive brand awareness.
- Prepare and deliver sales presentations and proposals to potential and existing clients.
- Monitor sales performance metrics and provide regular reports to senior management.
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