location_onGurugram, Haryana, India
watch_later Posted: Mar 08, 2025
Job Description
What will you do:
Key Responsibilities:
Education and Experience:
Key Responsibilities:
- Develop, implement, and maintain the QMS in alignment with ISO 13485:2016 standards. Create, review, and update QMS documentation, including quality policies, procedures, and work instructions.
- Support during External (Notified Body for ISO 13485:2016) and Corporate Audits and Provide real-time support to the auditors by delivering requested documents, records, and evidence.
- Maintain and update the Document Control System (Windchill) for controlled documents, including SOPs, work instructions, forms, and records.
- Ensure document revisions, approvals, and distribution align with company policies and regulatory requirements (ISO 13485, FDA, EUMDR, etc.).
- Coordinate with cross-functional teams to review and approve documentation.
- Maintain the periodic review the documents.Maintain and update the Learning Management System (SLMS) with training records.
- Track training completion rates and generate reports for management and audit purposes.Communicate training requirements to employees and provide reminders for upcoming deadlines.
- Assist in evaluating training effectiveness through feedback collection and performance metrics.Support internal and external audits by providing training records and evidence of compliance.
Education and Experience:
- BSC Biotechnology, B-Pharm / M-Pharm or related field from premier institutes
- 2-3 years of experience in Medical Device domain. At least 1+ years of experience in training and Document controller.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills. Proficiency in QMS software and tools.
- ISO 13485:2016 certification
- Excellent communication & interpersonal skills. High analytical skills.
- Able to run communicate effectively with senior leadership. Excellent problem-solving skills. Proactive to support both internal and external customers.
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