313 Patient Monitoring jobs in India

Company Overview

JD Healthcare Limited, a part of JD Lifesciences, is a dynamic company at the forefront of the medical device industry. With a focus on biomedical equipment and life-saving solutions, we provide innovative and quality products throughout India. Our dedication to reliability and excellence makes us a trusted partner to hospitals and healthcare institutions nationwide.

Job Overview

We are seeking a dedicated Ecommerce Specialist for our medical devices division, located in Nahur, Mumbai. This is a full-time, mid-level position requiring 4 to 6 years of work experience. The successful candidate will excel in driving our ecommerce strategies and proactively managing digital marketing initiatives within the healthcare sector.

Qualifications and Skills

• Proven experience in developing and implementing comprehensive digital marketing strategies tailored towards ecommerce platforms. (Mandatory skill)
• Expert knowledge in utilizing data analytics tools to measure site performance, understand consumer behavior and drive business growth. (Mandatory skill)
• Competency in ecommerce platform management with hands-on experience with platforms such as Shopify and WooCommerce. (Mandatory skill)
• Strong proficiency in product listing optimization aimed at improving visibility and conversion rates on various ecommerce platforms.
• Advanced skills in search engine optimization to enhance product searchability and increase organic traffic.
• Analytical mindset with the ability to interpret data and propose actionable business strategies.
• Excellent communication and teamwork skills for effective collaboration with internal and external stakeholders.

Roles and Responsibilities

• Develop and execute ecommerce strategies to drive sales growth for our medical device offerings.
• Manage day-to-day operations of ecommerce platforms, ensuring optimal performance and user experience.
• Coordinate with marketing teams to devise and implement digital campaigns aligned with business goals.
• Analyze consumer analytics and develop insights to refine marketing and sales strategies.
• Optimize product listings to improve searchability and increase conversion rates.
• Engage in SEO efforts to enhance visibility and ranking on search engines.
• Utilize CRM tools to manage customer interactions and improve service delivery.
• Collaborate with cross-functional teams to leverage business opportunities and drive profitability.

Careers that Change Lives

Role: Lab Engineer (Medical Devices)

Experience: 8 - 15 Years

Location: Hyderabad

Notice: 20 Days Less

The Technician will work in the R&D lab working majorly on setting up test fixtures, equipment trouble shooting, Equipment calibration and maintenance and support to engineers.

Sills sets: Laboratory Quality, QMS Auditing 17385, Changing the SOP, not dedicated quality

A Day in the Life

• Performs a variety of duties in the electronic, mechanical, electromechanical, and/or fabrication of prototype areas

• Fully understands the usage of test instruments and fixtures

• Constructs, troubleshoots, calibrates, adjusts, tests, diagnoses, and maintains equipment components, devices, or systems.

• Operates related equipment; conducts tests and reports data in prescribed format.

• Performs calibration and alignment checks; makes adjustments, modifications, and replacements as directed;

• Designing, documenting and executing various electrical and mechanical tests for the purposes of design characterization and design verification testing. Also includes preparation of devices for testing including, environmental preconditioning, temperature and humidity cycling.

• Document work as needed with respect to lab operations, using lab quality records and computer software (such as Excel/Word) as needed

• Follow procedures, methods and sequence of operations in performing daily tasks.

• Ensure all product, material, parts, and documentation are in compliance with company specifications and quality standards

• Actively contribute to ongoing continuous improvement efforts and projects

• Handle equipment as per operating procedures.

• Raising shopping carts and understands purchasing process

• Maintain overall lab in accordance with good laboratory practices

• Maintaining Lab 5's

Must Have: Minimum Requirements

• Minimum 8+ years of relevant experience and may require vocational or technical education or certification in addition to prior work experience

• BTech in Electrical or Mechanical required

Nice to Have

• 8+ years of work experience in electrical device or mechanical equipment handling in medical device industry

• Ability to use computer system and Microsoft Office product suite (Word, Excel, PowerPoint)

• Experience working in ISO certified lab environments

• Ability to read and comprehend instructions

• Ability to write correspondence, email and memorandums.

• Ability to learn new machines and procedures. Familiar with automated machinery

• Familiar with measuring tools and techniques.

• Training in Good Lab Practices (GLP)

We are seeking a skilled and motivated individual for handling work related to Medical Devices and Equipment sector. The person would be required to support the work of the Committees and Task Forces that provide recommendations and inputs on various policy matters regularly to Department of Pharma, MoHFW, National Health Authority, NITI Aayog, Department of Commerce and other related agencies, regulatory bodies as well as state governments. This is in addition to organising key events, roundtables and meetings with important stakeholders from government and industry, as well as raising sponsorships.

FICCI has been working in the healthcare sector for almost two decades and has been pivotal in facilitating interactions among stakeholders to jointly work towards affordable and accessible quality healthcare through different platforms and forums. Various FICCI Healthcare Committees and Task Forces have been providing valuable recommendations and strategies to the government on the key reforms launched by the government in recent years like Atmanirbhar Bharat, Medical Device Rules, Ayushman Bharat, Digital Health etc.

The job will involve compilation of regulatory and policy issues with the industry, preparing representations, actively engaging with the government on policy matters, and representing member companies to navigate the Indian medical device regulatory landscape.

Qualification and desired experience:

• Master's degree in Engineering/ Biotech, Pharma/Life Sciences, Biomedical Engineering, or related field with a focus on Government engagement and advocacy.
• 2+ Years of experience preferably in the Medtech/associated industries.
• Experience of working in a Chamber/Research based consulting company, associated with medtech sector will be preferred.
• Proven track record of effectively engaging with government departments and organizing advocacy events is desirable.

Competencies:

Technical (Knowledge, Skills, Attitude)

• Understand various policies and regulations in the Medical devices and equipment sector and their implications on the industry
• Strong understanding of medical device classification systems and regulatory pathways
• Understanding of dynamics and key issues in the Medtech industry
• Basic understanding of economics and financing
• Ability to conduct thorough desktop research to cull out relevant information
• Strong analytical skills
• Ability to prepare concept notes and collate relevant information from various stakeholders
• Ability to gauge industry needs and represent them in a cogent form to the relevant stakeholders
• Ability to plan, manage and execute large scale events and conferences
• Problem solving approach

Generic / Managerial

• Proficiency in English and Hindi language
• Excellent communication skills – written & verbal
• Ability to interact with senior stakeholders both from industry and government
• Good inter-personal skills
• Good presentation skills
• Adaptability and flexibility to undertake multiple tasks and to perform varied assignments
• Ability to manage and co-ordinate multiple assignments at a time
• Work as a team player
• Ability to meet deadlines

PRINCIPAL ACCOUNTABILITIES

• Track policy and regulatory changes in the sector and develop notes/representations/reports to regulator / Government, based on member inputs and FICCI research.
• Co-ordinate and liaise with research agencies on the development and publication of Knowledge Papers related to medtech sector. Collaborate with other departments within the association to align regulatory activities with broader industry goals.
• Stay updated on global trends in medical device regulations and identify potential implications for the Indian market. Conduct research and analysis on issues relevant to the industry, preparation of reports/papers
• Engage members in policy dialogues, taskforces and encourage stakeholders to take up FICCI membership
• Organise annual Conference and Expo, roundtables, workshops, webinars etc. prepare under the FICCI brand, assist in garnering sponsorships for the events; network with industry members for greater participation in FICCI initiatives
• Prepare and Develop Conference/event program, brochure, advertisement, PR plan, Social Media posts, pre and post event report, minutes of meetings etc.
• Work with other team members on sector specific initiatives, event management, logistics, database maintenance
• Prepare and maintain regular updates to senior management on monthly activities, annual report and other review documents

Careers that Change Lives

Role: Lab Engineer (Medical Devices)

Experience: 8 - 15 Years

Location: Hyderabad

Notice: 20 Days Less

The Technician will work in the R&D lab working majorly on setting up test fixtures, equipment trouble shooting, Equipment calibration and maintenance and support to engineers.

Sills sets: Laboratory Quality, QMS Auditing 17385, Changing the SOP, not dedicated quality

A Day in the Life

• Performs a variety of duties in the electronic, mechanical, electromechanical, and/or fabrication of prototype areas

• Fully understands the usage of test instruments and fixtures

• Constructs, troubleshoots, calibrates, adjusts, tests, diagnoses, and maintains equipment components, devices, or systems.

• Operates related equipment; conducts tests and reports data in prescribed format.

• Performs calibration and alignment checks; makes adjustments, modifications, and replacements as directed;

• Designing, documenting and executing various electrical and mechanical tests for the purposes of design characterization and design verification testing. Also includes preparation of devices for testing including, environmental preconditioning, temperature and humidity cycling.

• Document work as needed with respect to lab operations, using lab quality records and computer software (such as Excel/Word) as needed

• Follow procedures, methods and sequence of operations in performing daily tasks.

• Ensure all product, material, parts, and documentation are in compliance with company specifications and quality standards

• Actively contribute to ongoing continuous improvement efforts and projects

• Handle equipment as per operating procedures.

• Raising shopping carts and understands purchasing process

• Maintain overall lab in accordance with good laboratory practices

• Maintaining Lab 5's

Must Have: Minimum Requirements

• Minimum 8+ years of relevant experience and may require vocational or technical education or certification in addition to prior work experience

• BTech in Electrical or Mechanical required

Nice to Have

• 8+ years of work experience in electrical device or mechanical equipment handling in medical device industry

• Ability to use computer system and Microsoft Office product suite (Word, Excel, PowerPoint)

• Experience working in ISO certified lab environments

• Ability to read and comprehend instructions

• Ability to write correspondence, email and memorandums.

• Ability to learn new machines and procedures. Familiar with automated machinery

• Familiar with measuring tools and techniques.

• Training in Good Lab Practices (GLP)

We are seeking a skilled and motivated individual for handling work related to Medical Devices and Equipment sector. The person would be required to support the work of the Committees and Task Forces that provide recommendations and inputs on various policy matters regularly to Department of Pharma, MoHFW, National Health Authority, NITI Aayog, Department of Commerce and other related agencies, regulatory bodies as well as state governments. This is in addition to organising key events, roundtables and meetings with important stakeholders from government and industry, as well as raising sponsorships.

FICCI has been working in the healthcare sector for almost two decades and has been pivotal in facilitating interactions among stakeholders to jointly work towards affordable and accessible quality healthcare through different platforms and forums. Various FICCI Healthcare Committees and Task Forces have been providing valuable recommendations and strategies to the government on the key reforms launched by the government in recent years like Atmanirbhar Bharat, Medical Device Rules, Ayushman Bharat, Digital Health etc.

The job will involve compilation of regulatory and policy issues with the industry, preparing representations, actively engaging with the government on policy matters, and representing member companies to navigate the Indian medical device regulatory landscape.

Qualification and desired experience:

• Master's degree in Engineering/ Biotech, Pharma/Life Sciences, Biomedical Engineering, or related field with a focus on Government engagement and advocacy.
• 2+ Years of experience preferably in the Medtech/associated industries.
• Experience of working in a Chamber/Research based consulting company, associated with medtech sector will be preferred.
• Proven track record of effectively engaging with government departments and organizing advocacy events is desirable.

Competencies:

Technical (Knowledge, Skills, Attitude)

• Understand various policies and regulations in the Medical devices and equipment sector and their implications on the industry
• Strong understanding of medical device classification systems and regulatory pathways
• Understanding of dynamics and key issues in the Medtech industry
• Basic understanding of economics and financing
• Ability to conduct thorough desktop research to cull out relevant information
• Strong analytical skills
• Ability to prepare concept notes and collate relevant information from various stakeholders
• Ability to gauge industry needs and represent them in a cogent form to the relevant stakeholders
• Ability to plan, manage and execute large scale events and conferences
• Problem solving approach

Generic / Managerial

• Proficiency in English and Hindi language
• Excellent communication skills – written & verbal
• Ability to interact with senior stakeholders both from industry and government
• Good inter-personal skills
• Good presentation skills
• Adaptability and flexibility to undertake multiple tasks and to perform varied assignments
• Ability to manage and co-ordinate multiple assignments at a time
• Work as a team player
• Ability to meet deadlines

PRINCIPAL ACCOUNTABILITIES

• Track policy and regulatory changes in the sector and develop notes/representations/reports to regulator / Government, based on member inputs and FICCI research.
• Co-ordinate and liaise with research agencies on the development and publication of Knowledge Papers related to medtech sector. Collaborate with other departments within the association to align regulatory activities with broader industry goals.
• Stay updated on global trends in medical device regulations and identify potential implications for the Indian market. Conduct research and analysis on issues relevant to the industry, preparation of reports/papers
• Engage members in policy dialogues, taskforces and encourage stakeholders to take up FICCI membership
• Organise annual Conference and Expo, roundtables, workshops, webinars etc. prepare under the FICCI brand, assist in garnering sponsorships for the events; network with industry members for greater participation in FICCI initiatives
• Prepare and Develop Conference/event program, brochure, advertisement, PR plan, Social Media posts, pre and post event report, minutes of meetings etc.
• Work with other team members on sector specific initiatives, event management, logistics, database maintenance
• Prepare and maintain regular updates to senior management on monthly activities, annual report and other review documents