KLM Laboratories Hiring For Quality Control Dept
Job Requirement
Department: Quality Control (Reviewer)
Designation: Sr. Officer / Executive
Qualification: B. Pharm / M. Pharm Job
Location: Vadodara, Gujarat
Open Positions: 02
Experience: 4 to 7 years
Job Description
- Prepare and review Master Formula Record, Quality Manual, VMP, and SMF.
- Review AMV, STP, specifications, worksheets of finished and raw material packaging material.
- Review and implement validation protocols for process, equipment, cleaning, and analytical validation.
- Handle technology transfer at the site.
- Coordinate and participate in investigations of OOS, OOT, and incidents.
- Ensure compliance with GLP. Handle and review effectiveness of CAPA.
- Manage deviations and QMS-related activities, ensuring timely closure.
- Prepare and review process validation protocols and reports.
- Prepare APR and conduct trend analysis. Handle product recall and returned goods.
- Manage vendor qualification.
- Handle FDA license requirements.
- Maintain, control, and distribute documents; review for compliance with documentation procedures.
- Ensure effective implementation of data integrity.
- Ensure no unauthorized documents are in use for manufacturing and quality control.
- Manage stability studies: preparation, review, and approval of stability study protocols, reports, and summary reports.
Note: This is not a complete list of duties and responsibilities.
How to Apply: Interested candidates can send their updated resume to: career@klmlab.com
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| KLM Laboratories Hiring For Quality Control (Reviewer) Dept - Vadodara, Gujarat |
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