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Posted 17 June, 2026

HCLTech WalkIn Medical/Life science in Chennai on 30th May

HCLTech
Chennai, TN, IN Full Time
Reference: e2aa5e07c72479ab

Job Description

HCLTech Walkin Medical/Lifescience Hiring for Chennai Location on 30th May


Join a team that values innovation, growth, and impactful work. Don't miss the chance to work with cutting-edge Project in SME and be a part of something transformative!


Apply :


#DriveDate :30th May Saturday (9AM-2PM)


#ContactPerson : Katherine Sylvia


#VenueLocation : Chennai/Hyderabad

HCLTech Elcot Sez,

New Cafeteria 2nd Floor

602/3, 138, Medavakkam High Road,

Sholinganallur, Chennai-


Experience: 5-10 years


Job Location: Chennai , Hyderabad


Skill :


  • Global Complaints handling with medical device quality standards (FDA 21 CFR Part 820 and ISO 13485).
  • Post Market surveillance Investigating report writing


JD :


Key Responsibilities


Qualifications

  • Clinical Background: Bachelor’s degree or higher in a clinical or life sciences field (e.g., Nursing, Biomedical Engineering, Medicine, or equivalent healthcare experience)
  • Regulatory Knowledge: Hands-on experience with medical device quality standards (FDA 21 CFR Part 820 and ISO 13485).
  • Analytical Capability: Proven experience with statistical trending methodologies, data analysis tools, and technical scientific writing within a regulated environment.
  • Post Market surveillance Investigating report writing



Experience in,


  • Determining compliance dispositions for all identified trend signals, documenting technical rationales to justify whether escalation to a CAPA is required.
  • Authoring comprehensive Global Complaint Trending Signal Reports , ensuring meticulous documentation of the investigation scope, data analysis, and final risk-based conclusions.
  • Contributing to IPC reviews where applicable, mapping post-market field feedback to manufacturing operations and in-process controls to identify potential systemic source issues.
  • Collaborate with cross-functional teams—including Quality Engineering, R&D, and Medical Affairs—to conduct RCA on confirmed product trends.
  • Maintain audit-ready documentation that aligns with global regulatory standards



Contact Person : Katherine Sylvia


Interested candidates can share their CV on below mail id with Below details Current Company, Current CTC, Expected CTC, Notice Period, Location.

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