IPQA

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IPQA

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

Damaira Pharmaceuticals Private Limited

time outline iconBaddi, Himachal Pradesh, India

Posted on 18-09-2024

144 Views

1 Vacancy

Description

  • Monitor and verify the quality of products during various stages of the manufacturing process to ensure compliance with standard operating procedures (SOPs) and Good Manufacturing Practices (GMP).
  • Conduct in-process checks and inspections to ensure that production processes are running smoothly and products meet quality standards.
  • Maintain accurate and comprehensive records of in-process quality checks, including batch records, inspection reports, and any deviations observed.
  • Ensure proper documentation of all quality control activities and update records as needed for traceability and audits.
  • Ensure adherence to internal quality standards and regulatory requirements, including GMP, FDA, and other relevant guidelines.
  • Participate in internal and external audits, providing necessary documentation and information related to in-process quality assurance.
  • Assist in the preparation and execution of corrective and preventive actions (CAPA) based on audit findings.
  • Identify and investigate deviations or non-conformities observed during the manufacturing process.
  • Document deviation reports and collaborate with relevant departments to implement corrective and preventive actions.
  • Follow up on the resolution of deviations to ensure that issues are addressed and preventive measures are in place.

Category

Pharmaceuticals

Functional Area

Pharma IPQA

Preferred Education

Science Graduate

Key Skills

Attention to DetailTeam WorkCommunicationPositive AttitudeIPQA

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