QA-Documentation Specilaist At Techno Pharmaceuticals |
0: 3 years of experience|Science Vacancy
Performs Q.A document control functions, documentation and record keeping processes conform to cGMP, regulatory requirement and documentation system procedure.
1.Performs Q.A document control functions, including the issuance document processing, document login, tracking, stamping, review, distribution and archiving of documents to ensure documentation and record processes conform to cGMP, GDP and regulatory requirement.
2.Checks the version of the received procedures for review conducted prior to its issuance to ensure the original and current version of the procedures placed in documentation system.
3.Reviews Batch Production Records Masters before issuance activities to make sure they comply with the master currently version and requirements of the Good Documentations Practices (GDP) regulation, required standards and regulations.
4.Retrieves the old (obsolete / with due date) copy, then delivers it to the archivist for destruction issues to ensure that is no invalid document.
5.Organizes and files the valid and obsolete documents to ensure accurate and reliable filing systems for all paper-based GMP documents.
6.Communicates with QA Document Control Senior Assurer about notes and remarks to get timely feedback on related issues.
7.Follows and Applies quality, environment and occupational safety and health systems to fulfil legal requirements and other requirements of the good manufacturing regulations of WHO guideline and international standards.
Education: Bachelor ‘s Degree in Science, Pharmacy or Agriculture
Years of Experience: 1
Application End Date: 14 May 2023
Available Vacancies: 1
Job Level: Specialist
Function: QA - Documentation