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QA-Documentation Specilaist At Techno Pharmaceuticals | 0: 3 years of experience|Science Vacancy

 QA-Documentation Specilaist At Techno Pharmaceuticals | 

0: 3 years of experience|Science Vacancy

QA-Documentation Specilaist At Techno Pharmaceuticals | 0: 3 years of experience|Science Vacancy


Summary:

- Performs Q.A document control functions, documentation and record keeping processes conform to cGMP, regulatory requirement and documentation system procedure. - Assists in the day to day document and record management activities which are complying with PHARCO Pharmaceuticals procedures and regulatory requirement.


Job requirements:

·         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.


·         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.


·         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.


·         Retrieves the old (obsolete / with due date) copy, then delivers it to the archivist for destruction issues to ensure that is no invalid document.


·         Organizes and files the valid and obsolete documents to ensures accurate and reliable filing systems for all paper-based GMP documents.


·         Communicates with QA Document Control Senior Assurer about notes and remarks to get timely feedback on related issues.


·         Follows and Applies quality, environment and occupational safety and health systems to fulfill legal requirements and other requirements of the good manufacturing regulations of WHO guideline and international standards.


General Responsibilities:


-          Compliance with internal regulations and the company's policies and procedures.


-          Compliance with Sector/Department SOPs.


-          Follow and apply the requirements of ISO 9001/2015,14001/2015 and 45001/2018.


Qualifications:


Bachelor of Science


0: 3 years of experience in Q.A (Experience in Pharmaceutical is preferred)



Good commands in English language


Good skills in MS Excel, MS Power Point, MS Visio, MS Word & Oracle

Years of Experience: 0


Posting Date: 1 April 2021


Application End Date: 30 April 2021


Available Vacancies: 1


Job Level: Specialist


Function: QA - Documentation

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