QA Specialist - Document Control at Eva Pharma

, , Saudi Arabia -

Full Time

Start Date

Immediate

Expiry Date

11 Apr, 26

Salary

0.0

Posted On

11 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Document Management, Quality Assurance, Regulatory Compliance, SOP Review, Change Control, Validation Packages, Training Coordination, Version Control, Audit Readiness, Attention to Detail, Communication Skills, Collaboration, Microsoft Office, Document Management Systems

Industry

Pharmaceutical Manufacturing

Description

Join EVA Pharma, a leading pharmaceutical company committed to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are dedicated to fostering a supportive and innovative environment for our team members. We are looking for a meticulous and dedicated QA Specialist – Document Control to join our Quality Assurance team at EVA Pharma's factory in Hautat Sudair, Riyadh Province, Saudi Arabia.. The ideal candidate will play a crucial role in ensuring that all quality-related documents are managed effectively, adhering to regulatory requirements and best practices. Key Responsibilities: Establish and maintain a robust document management system for all quality assurance documentation, ensuring compliance with applicable regulations and internal standards. Review and approve quality documents, including SOPs, change controls, and validation packages, ensuring accuracy and completeness. Coordinate the training and distribution of updated quality documents to relevant stakeholders within the organization. Monitor document changes and ensure proper version control, archiving, and retrieval of documents as needed. Assist with internal and external audits related to document control processes and maintain audit readiness. Bachelor’s degree in a related field such as Life Sciences, Pharmacy, or Quality Management. 1–3 years of experience in quality assurance or document control within the pharmaceutical or related industry. Strong understanding of regulatory requirements (cGMP, GDP, etc.) and quality management principles. Excellent organizational skills with high attention to detail and accuracy. Strong communication skills and ability to work collaboratively with cross-functional teams. Proficient in Microsoft Office Suite; experience with document management systems is a plus.

Responsibilities

The QA Specialist will establish and maintain a document management system for quality assurance documentation and ensure compliance with regulations. They will also review and approve quality documents and assist with audits related to document control processes.