Job Description

ORTHRYA (Conlis Global Inc. India) is looking for a hands-on professional to lead ISO 13485–compliant manufacturing operations and manage clinical trials across India for our innovative medical devices.

Location: Delhi.

Candidate must have flexibility to travel

Key Responsibilities:

• Oversee ISO 13485 QMS and manufacturing operations

• Lead audits, CAPAs, supplier quality, and process validation

• Manage and coordinate multi-site clinical trials across India

• Liaise with hospitals, investigators, CROs, ethics committees, and regulators

• Ensure compliance with CDSCO, ICMR, and GCP guidelines

Ideal Profile: (Minimum 1-3years experience)

• Experience in medical device manufacturing & quality systems

• Strong understanding of ISO 13485 and clinical operations

• Highly flexible with travel and on-site execution

• Proactive, detail-oriented, and execution-driven

• Highly motivated and self driven

• Previous experience with medical device manufacturing is highly desirable

Qualifications:

• M.Tech or M.Sc. in in Biological Sciences, Biomedical Engineering, Medical Devices

• In-depth knowledge of ISO certifications for medical devices is highly desirable.

•Experience with managing and conducting clinical trails with devices is highly desirable

• Exceptional communication, organizational, and analytical skills.

• Proven ability to work independently and collaboratively in a dynamic environment.

Send your CV to sumritabhat@conlisglobal.com