Lavipharm is looking for a Quality Assurance Associate who will create/handle the documentation for the quality processes of the organization.
Job position reports to Lead Quality Assurance.
Responsibilities
• Follows the instructions of the Quality Assurance Lead and the general principles of the Company's policy
• Assists with other cross-functional teams to ensure company's goals and objectives are met
• Archives all qualification / validation protocols, product manufacturing files (BMR) and all QA & QC documentation
• Is in charge of the Documentation system for all departments in the plant including:
- Issuance and distribution of all SOP’s, protocols and QC specifications
- Follow up and update of the relevant indexes
- Cancellation and filing of obsolete documents
• Collates and files the expenses of the QA & QC departments
• Liaises with all departmental suppliers and clients
• Assists in preparation of packing lists for export activities
• Delivers timely and effective administration support to the quality function and the ongoing maintenance of quality systems and databases
• Maintains effective information storage systems to enable easy retrieval of QA/QC documents and data
• Maintenance of all records demonstrating full traceability of changes to management system
• Inputs to the ongoing improvement of quality systems and applications
• Communicates with customers and associates of the company in accordance with the applicable Quality requirements
• Bachelor of Science (BSc) Degree in Life Science preferred.
• 1-3 years experience in in the Pharma industry within the Quality function is preferred.
• Computer Literacy (MS Office, ERP Systems etc.)
• Excellent knowledge of the English language
Skills
• Excellent attention to detail, project and time management skills, and the ability to manage multiple priorities with aggressive timelines
• Excellent written and verbal communication skills
• Effective organization and planning skills
• Good interpersonal, communication and team collaboration skills and strong collaborative mindset
If you are ready to embark into challenging endeavors, be exposed to continuous learning opportunities, you are interested in the above position and only if you have the required qualifications, please reply, enclosing your curriculum vitae.
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Lavipharm is on the lookout for a dedicated Quality Assurance Associate to join our dynamic team! As a Quality Assurance Associate, you’ll be at the heart of our operations, responsible for managing and creating documentation that ensures our quality processes run smoothly. Reporting to the Lead Quality Assurance, your role will encompass a variety of exciting responsibilities. You’ll collaborate with cross-functional teams to align with company goals and objectives, manage vital documentation including SOPs and QC specifications, and maintain files that demonstrate the highest standards of quality control. Your organizational skills will shine as you archive all qualification, validation protocols, and product manufacturing files, keeping our systems efficient and structured. The role also entails liaising with suppliers and clients, assisting with packing lists for export activities, and providing timely administrative support to maintain our quality systems and databases. We seek someone with a Bachelor of Science in Life Science, preferably with 1-3 years in the Pharma industry focusing on quality. If you thrive in a fast-paced environment and possess excellent attention to detail as well as strong communication skills, this is your chance to make a significant impact. Join us at Lavipharm, where continual learning and growth are part of our ethos. If you have the qualifications and enthusiasm for this position, we’d love to hear from you!
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