- Conduct in-process inspections of semi-finished and finished products
- Document all reports and maintain accurate records
- Analyze non-conforming products and develop action plans
- Audit process parameters in clean rooms and controlled areas
- Handle market complaints and resolve issues
- Manage the development of packaging materials
- Oversee testing of raw materials, packing materials, and finished goods
- Review documents and records for compliance
- Knowledge of GMP and QMS standards
- Regulatory affairs procedures and documentation
- Ability to analyze data and develop actionable insights
- Strong communication and interpersonal skills
- Ability to work independently and as part of a team
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Quality Assurance-Reputed Pharma Industry-Hyderabad, Telangana, India-4LPA-Harshala - Seven Consultancy
Description
Job Summary
We are seeking a Quality Assurance professional to join our team at Seven-Consultancy. The ideal candidate will have extensive knowledge of GMP and QMS standards, regulatory affairs procedures, and documentation.
The successful candidate will be responsible for conducting in-process inspections of semi-finished and finished products, documenting all reports, maintaining discipline in controlled areas, analyzing non-conforming products, and developing action plans.
In addition, the candidate will be required to audit process parameters in clean rooms and controlled areas, handle market complaints, manage the development of packaging materials, and oversee testing of raw materials, packing materials, and finished goods.
The selected candidate will also review documents and records, ensuring compliance with ISO 13485, WHO, GMP, and CE Marking regulations.
Key Responsibilities:
Requirements:
Functional Area:
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