Job ID R-514644 Date posted 21 abril 2025

Sea parte de algo más grande en BD. Aquí, nos ayudará a compartir nuestras soluciones innovadoras con más clínicas, médicos, farmacias y entidades médicas que, a su vez, beneficiarán la salud y el bienestar de las personas y los pacientes de todo el país. Es un puesto emocionante, desafiante y gratificante, pero trabajará desde una posición sólida gracias a nuestro nombre de confianza y la convicción que desarrollará rápidamente en nuestros productos . Aquí, canalizará todas sus habilidades y experiencia en ventas hacia un único objetivo: impulsando el mundo de la salud™. En BD, puede hacer una verdadera diferencia.

  • Tipo de trabajo:
    Tiempo completo
  • Nivel del puesto:
    Ingreso a personas mayores
  • Viajes:
    Varía
  • Salario:
    Competitivo
  • Glassdoor Reviews and Company Rating

Responsibilities

Job Description Summary

About BD

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. The company develops innovative technology, services and solutions that help advance both clinical therapy for patients and clinical process for health care providers. BD has 70,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.


About BD TCI

BD, a 125-year-old global medical device company has started its Enterprise Center in Bangalore, India called BD Technology Campus India (TCI). This Enterprise Center will be an integral part of the global network for BDX. It will have presence of R&D, Quality, Regulatory, IT and other functions. The center boasts of some of the brightest minds who work in a unique environment that fosters and supports ingenuity. BD TCI is dedicated to serving BD’s customers and patients thereby contributing its bit towards “advancing the world of health”.



Position Summary

Performs Post Market Surveillance (PMS) activities to ensure compliance with applicable medical device regulations.Ensures data collection, compilation, cross-functional reviews, and final release of PMS Plans, PMS Reports, and PSURs per EU MDR and regional regulatory requirements. Works under general direction while independently determining and developing approaches to solutions, with frequent inter-organization collaboration required.



Educational Background

Bachelor’s degree in engineering, or a technical discipline.



Professional Experience

3+ years of relevant experience required, preferably in the Medical Device / Healthcare Industry



Job Responsibilities

      Supports PMS process in accordance with EU MDR 2017-745 and regional regulations. 
      Compiles device-based PMS Plans, PSUR and regional PMS reports, ensuring consistency and accuracy in information, data analysis, content and layout, spelling, grammar, punctuation, and compliance to regulation and procedure.
Works collaboratively with the cross-functional teams to meet all specified requirements and timelines, supporting multiple projects simultaneously.
Supports internal/external audits and related assignments.
      Supports continuous improvement objectives for Quality Systems and Post Market Surveillance organization.
      Administers appropriate PMS training as needed.
      Participates in the ongoing operations of QA/QS activities and performs related duties as assigned.


​Knowledge and Skills
Knowledge


Knowledgeable in medical device post market surveillance and risk management regulations and practices (EUMDR 2017-745, ISO 13485, ISO 14971, FDA QSR, etc.)
Proficient in data analytics with demonstrated experience in Microsoft Power BI and Microsoft Excel.
Excellent technical writing skills. Disciplined and well-organized in documentation, with high proficiency level required in Microsoft Word and Adobe Acrobat.
Working knowledge of Good Documentation Practices in prior roles.


Skills

Team player with excellent interpersonal and communication skills, with ability to review and work through complexities in a methodical manner.
Fluent in English language (spoken and written) as the main mode of communication across teams and functions.
Strong critical thinking, analytical, and problem-solving skills.


Desired / Additional Skills & Knowledge (Not essential to the job but will be an advantage to possess)
      Familiarity with Microsoft Vizio application.

Any additional Information (Specially if needed for Quality or legal purposes)
N/A

Job Description

P2-14200

About BD

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. The company develops innovative technology, services and solutions that help advance both clinical therapy for patients and clinical process for health care providers. BD has 70,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.


About BD TCI

BD, a 125-year-old global medical device company has started its Enterprise Center in Bangalore, India called BD Technology Campus India (TCI). This Enterprise Center will be an integral part of the global network for BDX. It will have presence of R&D, Quality, Regulatory, IT and other functions. The center boasts of some of the brightest minds who work in a unique environment that fosters and supports ingenuity. BD TCI is dedicated to serving BD’s customers and patients thereby contributing its bit towards “advancing the world of health”.

Position Summary

Performs Post Market Surveillance (PMS) activities to ensure compliance with applicable medical device regulations. Ensures data collection, compilation, cross-functional reviews, and final release of PMS Plans, PMS Reports, and PSURs per EU MDR and regional regulatory requirements. Works under general direction while independently determining and developing approaches to solutions, with frequent inter-organization collaboration required.

Educational Background

Bachelor’s degree in engineering, or a technical discipline.

Professional Experience 

3+ years of relevant experience required, preferably in the Medical Device / Healthcare Industry

Job Responsibilities

      Supports PMS process in accordance with EU MDR 2017-745 and regional regulations. 
      Compiles device-based PMS Plans, PSUR and regional PMS reports, ensuring consistency and accuracy in information, data analysis, content and layout, spelling, grammar, punctuation, and compliance to regulation and procedure.
Works collaboratively with the cross-functional teams to meet all specified requirements and timelines, supporting multiple projects simultaneously.
Supports internal/external audits and related assignments.
      Supports continuous improvement objectives for Quality Systems and Post Market Surveillance organization.
      Administers appropriate PMS training as needed.
      Participates in the ongoing operations of QA/QS activities and performs related duties as assigned.


​Knowledge and Skills
Knowledge


Knowledgeable in medical device post market surveillance and risk management regulations and practices (EUMDR 2017-745, ISO 13485, ISO 14971, FDA QSR, etc.)
Proficient in data analytics with demonstrated experience in Microsoft Power BI and Microsoft Excel.
Excellent technical writing skills. Disciplined and well-organized in documentation, with high proficiency level required in Microsoft Word and Adobe Acrobat.
Working knowledge of Good Documentation Practices in prior roles.


Skills

Team player with excellent interpersonal and communication skills, with ability to review and work through complexities in a methodical manner.
Fluent in English language (spoken and written) as the main mode of communication across teams and functions.
Strong critical thinking, analytical, and problem-solving skills.


Desired / Additional Skills & Knowledge (Not essential to the job but will be an advantage to possess)
      Familiarity with Microsoft Vizio application.

Any additional Information (Specially if needed for Quality or legal purposes)
N/A

Required Skills

Optional Skills

.

Primary Work Location

IND Bengaluru - Technology Campus

Additional Locations

Work Shift

Aplicar

Success Profile

¿Qué hace exitoso a un profesional en Calidad en BD? Echa un vistazo a los principales rasgos que estamos buscando y mira si tienes la combinación adecuada.

  • Ambicioso
  • Colaborativo
  • Orientado a objetivos
  • Persuasivo
  • Orientado a resultados
  • Emprendedor

Avances en el mundo de la salud™

BD es una de las compañías de tecnología médica más grandes del mundo y está mpulsando el mundo de la salud™ al mejorar el descubrimiento médico, el diagnóstico y la entrega de cuidado. BD ayuda a los clientes a mejorar los resultados, reducir los costos, aumentar la eficiencia, mejorar la seguridad y ampliar el acceso a la atención médica.

BD es único en cómo se dedica completamente a un estado de enfermedad específico. Deja en claro cómo el trabajo que hacemos impacta directamente en la vida diaria de los pacientes que atendemos.


Eric Rainis
Director sénior de gestión de calidad

Saber que nuestros productos llegan a 30 millones de personas con diabetes en todo el mundo es poderoso y alimenta a nuestros equipos para ofrecerles los mejores productos de su clase todos los días.


Bridget Bagnato
Inyección VPGM

Es inspirador ver que los productos de BD se utilizan en todo el mundo para promover el cuidado de la salud humana.


Yang Zeng
Gerente Medico de Laboratorio

BENEFITS

Cuidado de la salud

401(k)/
Planes de jubilación

Desarrollo profesional

Tiempo libre pagado

Premios y
reconocimientos

Working in

Bengaluru

Take a look at the map to see what's nearby.

No se lo pierda

Reciba alertas de empleo personalizadas según su función y/o criterio de búsqueda de ubicación.

Interested in

Únase a nuestro grupo de talentos

Únase a nuestro grupo de talentos

Upload your resume to help our recruiters match you to the right job. They'll be in touch if they find a good fit.

Aviso de fraude de BD

Tenga en cuenta las publicaciones de trabajo potencialmente fraudulentas en otros sitios web o correos electrónicos o mensajes de texto de reclutamiento sospechosos que intentan recopilar su información confidencial. Si le preocupa que una oferta de empleo con BD, CareFusion o CR Bard pueda ser una estafa, verifique buscando la publicación en la página de carreras o contáctenos en ASC.Americas@bd.com. Para obtener más información, haga clic aquí.