Dosimetrist

**Position Overview**:
**Key Responsibilities**:

- Establish, implement, and maintain the quality management system for Vishvesh Agromed Private Limited in accordance with International Standards ISO 9001:2008 and ISO 11137-1.
- Conduct comprehensive internal quality audits to verify the implementation and maintenance of the quality system, ensuring compliance with established procedures and standards.
- Publicize the quality objectives and policy statement of Vishvesh Agromed Private Limited and ensure understanding, implementation, and maintenance at all levels of the organization.
- Approve the quality manual after review by the quality assurance department and incorporation of suggested changes.
- Distribute and maintain the quality assurance manual and associated documentation, ensuring controlled copies accurately describe the quality system and contain all revisions resulting from management reviews and changes to ISO standards.
- Initiate periodic management reviews of the quality system to ensure its suitability and effectiveness, implementing corrective and preventive actions as necessary.
- Report to the In-charge regarding the performance and improvement needs of the quality management system.
- Represent Vishvesh Agromed Private Limited for quality evaluations conducted by external assessors and customers.
- Promote understanding of customer requirements and the quality management system through training seminars for key personnel.
- Interact with the In-charge and section officers to resolve customer complaints and quality problems effectively and promptly.

**Additional Responsibilities**:

- Perform plant dosimetry, dose mapping, dose validation, and routine dosimetry activities.
- Identify, evaluate, and record actual and potential quality problems within the facility.
- Initiate, recommend, and provide corrective and preventive measures, verifying their implementation.
- Review Quality Manual, Validation Protocols, and Site Master File.
- Review execution schedules for preventive maintenance, calibration, and process validation.
- Review SOPs and methods for compliance with GMP norms.
- Ensure testing is carried out as per specifications.
- Review validation protocols/reports and deviation records.
- Handle investigation of client complaints, batch failures, and OOS.
- Review change controls and Corrective and Preventive Actions (CAPA).
- Handle regulatory visits and matters.
- Identify training needs in line with GMP norms.
- Carry out process validation activities.
- Handle or oversee reprocessing activities.
- Review batch documents and release them for further processing.

Pay: ₹15,000.00 - ₹23,000.00 per month

**Benefits**:

- Health insurance
- Provident Fund

Schedule:

- Day shift

Supplemental pay types:

- Performance bonus

Work Location: In person

Expected Start Date: 01/06/2024