Quality Assurance Associate

🕒 February 16

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SGS

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1878

📋 Compliance

☁️ SaaS

Compliance • SaaS • Sustainability

SGS is the world's leading Testing, Inspection, and Certification (TIC) company, providing a comprehensive range of services designed to assure quality and integrity across various sectors. SGS is focused on sustainability, offering climate action services and an all-encompassing ESG portfolio under its IMPACT NOW suite. The company has ambitious targets for growth by 2027, driven by its strategy to address global megatrends. SGS operates globally, providing business assurance, connectivity and products, digital trust, health and nutrition, and solutions for industries and the environment.

📋 Description

• Review and approve Change Control Request and ensure their timely closure by coordinating with owners. • Act as site representative for Trainings and Document Control systems and manage related activities. • Maintain client test methods, specification databases, and coordinate Quality Agreement approvals internally, externally, and with Legal. • Coordinate and support internal, client, and regulatory audits, and prepare responses to audit findings. • Act as backup for QA functions, including release of Certificates of Analysis, vendor evaluations, and other QA management responsibilities. • Follows Training SOP for training and training records. • Review and approve CCRs and coordinate for their timely closure by periodic follow up with associated CR owners. • Responsible for keeping track of upcoming periodic reviews of documents and ensure their timely completion. • Set up all the documents in DMS and coordinate for their approvals. • Be site representative for Trainings and Document control systems and manage all the activities for these programs.

🎯 Requirements

• Bachelor’s degree related to scientific area is required. • Minimum 3 years working experience in Quality Assurance in Pharma industry is required. • Demonstrated understanding of relevant GMP (Good Manufacturing Practice) regulations is required. • Knowledge in compendiums such as USP is preferred. • Proficiency in Microsoft Office applications, including Outlook, Word, and Excel. • Ability to learn quickly new technologies. • Excellent written and strong verbal communication skills in English (C1). • Protocol and report writing compliant with regulatory standards.

🏖️ Benefits

• Health insurance • Paid time off • Professional development opportunities