QA Executive (Process/Cleaning Validation)
6 - 8 Years of ExperienceNot disclosed Full Time
Sidmak Laboratories Pvt. Ltd.
Dehradun, Uttarakhand, India
Posted on 25-12-2023
566 Views
1 Vacancy
Description
Quality Systems Development:
- Develop, implement, and maintain the organization's quality management system.
- Establish and update quality policies, procedures, and documentation.
Audits and Inspections:
- Conduct internal audits to assess compliance with quality standards and regulations.
- Prepare for and participate in external audits by regulatory bodies.
Process Compliance:
- Monitor and ensure adherence to cGMP (current Good Manufacturing Practice) and other relevant standards.
- Identify non-conformities and implement corrective and preventive actions.
Documentation Control:
- Manage and control documentation related to quality assurance.
- Ensure that documents are up-to-date, accurate, and accessible.
Training and Development:
- Provide training on quality systems and procedures to employees.
- Foster a culture of quality awareness and continuous improvement.
Change Control:
- Review and approve changes to processes, procedures, and specifications.
- Assess the impact of changes on quality and compliance.
Product Release:
- Collaborate with production and quality control to review and release finished products.
- Ensure that products meet quality standards before release.
Customer Complaints:
- Investigate and address customer complaints related to product quality.
- Implement corrective and preventive actions based on complaint trends.
Supplier Quality Management:
- Evaluate and monitor the quality performance of suppliers.
- Conduct supplier audits and assessments.
Category
Pharmaceuticals
Functional Area
Pharma Quality Assurance (QA)
Preferred Education
MSc (Master of Science)MPharm (Master Of Pharmacy)BSc (Bachelor of Science)BPharm (Bachelor Of Pharmacy)
Key Skills
Collaboration SkillsCommunication SkillsTeamworkProblem Solving Skills
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