Officer/Sr. Officer-QA

Officer/Sr. Officer-QA

work outline icon2 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Umedica Laboratories Limited

time outline iconVapi, Gujarat, India

Posted on 26-11-2024

110 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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