What are the responsibilities and job description for the Validation Engineer (Medical Devices) position at TekOne IT Services Pvt. Ltd.?
Role: Lab Instrument Qualification Specialist
Location: New Brunswick, NJ
Duration: 12 Months
Key Responsibilities
Location: New Brunswick, NJ
Duration: 12 Months
Key Responsibilities
- Author and manage URS, IQ/OQ/PQ documents.
- Execute and facilitate equipment qualification activities.
- Ensure compliance with GMP, FDA, and ISO standards.
- Qualifications:
- Bachelor’s degree in Chemistry or related field.
- 3-5 years of experience in instrument qualification.
- Familiarity with ALCOA principles and Data Integrity.
