Sr. Officer

1 week ago

goa, India Molbio Diagnostics Full time

Qualification

M.Sc / B.Pharm / M.Pharm


Experience

3 - 5 Yrs. in Pharmaceutical / Medical Device Industry


Job Summary

We are seeking a dedicated and detail-oriented Quality Assurance professional to join our Quality Management System (QMS) section. The ideal candidate will assist in maintaining and improving QMS function, ensuring compliance with regulatory standards and internal policies.


Key Responsibilities:

Documentation and Record Management:

  • Assist in the preparation, review, and maintenance of quality assurance documentation, including SOPs, protocols, and reports.
  • Ensure proper documentation control and record-keeping practices.


Compliance and Audit Support:

  • Support internal and external audits by preparing necessary documents and records.
  • Assist in implementing corrective and preventive actions (CAPAs) based on audit findings.


Quality Systems Monitoring:

  • Participate in the monitoring and maintenance of quality systems, including deviation management, change control, and risk assessments.
  • Help ensure compliance with GMP, GLP, and other relevant regulatory requirements.


Training and Development:

  • Assist in organizing and conducting training sessions for staff on QMS-related topics.
  • Maintain training records and ensure that personnel are adequately trained.


Continuous Improvement:

  • Support continuous improvement initiatives within the QMS framework.
  • Collect and analyze data to identify trends and areas for improvement.

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