Officer/Sr. Officer-QA
2 - 5 Years of ExperienceNot disclosed Full Time
Umedica Laboratories Limited
Vapi, Gujarat, India
Posted on 26-11-2024
43 Views
1 Vacancy
Description
- Process Monitoring: Oversee manufacturing processes to ensure they comply with established quality standards and procedures.
- Documentation Review: Inspect and approve documentation, including batch records, test results, and SOPs, for accuracy and completeness.
- Audits: Conduct internal audits and support external audits to ensure compliance with regulatory requirements and company policies.
- Quality Testing: Collaborate with the QC team to verify that raw materials, in-process samples, and finished products meet quality specifications.
- CAPA Management: Identify non-conformities, investigate root causes, and implement corrective and preventive actions (CAPA).
- Training: Provide training to employees on quality policies, GMP, and regulatory compliance to maintain a high-quality culture.
- Regulatory Compliance: Ensure all products, processes, and systems adhere to relevant industry standards and regulations, such as ISO, GMP, or FDA.
- Risk Assessment: Analyze potential risks in production and implement measures to mitigate quality issues.
- Continuous Improvement: Develop and implement strategies to improve processes, enhance product quality, and reduce defects.
- Reporting: Prepare and present detailed quality reports, including trends, deviations, and performance metrics, to management.
Category
Pharmaceuticals
Functional Area
Pharma Quality Assurance (QA)
Key Skills
Communicationproblam solvingAttention to DetailPositive Attitude
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