Grow With Us

Build a Career That Touches Millions of Lives

For over 70 years, Sterimed has manufactured the medical and surgical disposables clinicians rely on across 50+ countries. Join a team of engineers, quality specialists, clinicians and commercial professionals building safe, dependable, life-saving technology — every single day.

Career with Sterimed Group

Our Culture

Why Clinicians & Professionals
Join Sterimed

Work in an environment built around quality, integrity, and clinical focus

Innovate with Purpose

Innovate with Purpose

Develop products used in critical care, anaesthesia and surgery that reach millions of patients worldwide. Your work has measurable clinical impact.
Global Footprint

Global Footprint

Contribute to medical solutions exported to 50+ countries, manufactured to ISO 13485, CE and WHO-GMP standards trusted by health systems around the world.
Advanced Manufacturing

Advanced Manufacturing

Work alongside modern extrusion, moulding and assembly lines in WHO-GMP certified cleanroom environments built for precision and scale.
Grow through structured learning tracks

Learn from the Best

Grow through structured learning tracks and mentorship from veterans in biomedical engineering, regulatory affairs, quality and production.

Job Board

Explore Current Openings

Find the role that fits your skills and ambitions

Responsibilities

  • Design and refine airway-management consumables (such as endotracheal tubes and cuffs) to meet clinical and regulatory standards.
  • Test and evaluate polymer materials and thermo-sensitive PVC compounds.
  • Collaborate with clinical specialists and tooling designers on prototyping.

 

Requirements

  • Bachelor's / Master's in Biomedical or Polymer Engineering.
  • 2–5 years of product-design experience in medical plastics.
  • Proficient with SolidWorks or equivalent CAD tools.

Responsibilities

  • Ensure manufacturing stages comply with ISO 13485:2016 and WHO-GMP guidelines.
  • Draft quality assurance document protocols, cleanroom audit schedules, and batch reviews.
  • Investigate non-conformances and oversee corrective and preventive actions (CAPA).

 

Requirements

  • B.Pharma, M.Sc., or B.Tech in Biotechnology/Chemical Engineering.
  • 3+ years of QA experience in sterile medical device manufacturing.
  • Thorough understanding of CE/MDD audits and cleanroom protocols.

Responsibilities

  • Drive export sales growth for Sterimed medical devices across regional portfolios (EU, LATAM, APAC).
  • Nurture relationships with regional distributors and clinical procurement channels.
  • Represent Sterimed Group at international medical trade fairs (such as MEDICA, Arab Health).

 

Requirements

  • MBA in Sales/Marketing or International Business.
  • 5+ years of export sales experience in disposable medical consumables.
  • Excellent communication and negotiation skills.

Responsibilities

  • Supervise shift production targets in cleanrooms, managing extrusion and assembly processes.
  • Optimize raw material utilization and ensure operator compliance with safety standards.
  • Maintain daily production logs and batch records.

 

Requirements

  • Diploma / Degree in Mechanical / Production Engineering or Plastic Technology.
  • 2-4 years of supervisory experience in assembly line operations.
  • Familiarity with lean manufacturing concepts (5S, Kaizen).

Apply Now

Submit Your Application

Submit your details and CV, and our recruitment team will reach out to you

    Ultrasil

    At Sterimed Group we take pride in delivering quality consistently for over 70 years, and growing on the trust and goodwill of healthcare and industrial partners worldwide.

    Company

    Products

    Contact

    Sterimed Surgicals (India) Pvt. Ltd.
    Regd. Office: 501, Ring Road Mall, Manglam Place Sector-3, Rohini, New Delhi-110085 (INDIA)

    Phone
    +91 9424661960

    Email
    ultrasil@sterimedgroup.com

    © 2026 Sterimed Group (Ultrasil Silicone Solutions). All Rights Reserved.

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