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Junior QA Batch Record Reviewer
Capgemini Engineering recherche un Junior QA Batch Record Reviewer pour examiner des dossiers de lots électroniques et soutenir leur libération par la qualité. Le poste implique une collaboration avec les équipes Manufacturing et Quality ainsi que la gestion de dossiers qualité liés aux écarts et CAPA. Une expérience de 1 à 3 ans en revue de dossiers de lots ou en fabrication est requise, dans un environnement pharmaceutique ou API réglementé GDP et GMP.
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The full description published by Capgemini Engineering.
Description de l’offre
At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as they provide unique R&D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days are the same.Job Description
Your role
We are seeking a Junior QA Batch Record Reviewer for our client located in Visp.
Your Responsibilities
Perform timely and independent review of executed electronic batch records (eBRs) in MES Syncade. Ensures that operations batch records are accurately executed, complete, and ready for QA review.
Collaborate with Manufacturing and Quality teams to clarify and resolve documentation issues Initiate and support in the management of Quality Records (CAPAs and Deviations) for Batch Record review related observations.
Support preparation of documentation package to enable fast release by QA.
Your skills and experience1-3
years of experience in batch record review (preferred eBR) OR in manufacturing is required.Previous experience in GDP and GMP regulated pharmaceutical / API industry. Ability to identify non-compliance and gaps from quality standards. Very good communication skills and interaction with all kinds of interfaces within the organization; strong team orientation. Structured, focused and well-organized working attitude. Open-minded for new ideas and suggestions; solution-oriented. Agile, highly motivated and dynamic drive. Ability to produce reliable results under stress.
What you’ll love about working here
At our engineering academy, you’ll have access to over 60,000 hours of world-class training - designed to fuel your growth from day one.
Whether you're diving into Generative AI, data science, or sustainability, our digital campus supports your learning journey every step of the way;Experience the benefits of hybrid working, offering flexibility and ensuring work-life balance;Harness the strength of diverse teams, fostering innovation and inclusive collaboration;We offer additional benefits such as 5 weeks of vacation, Employee referral bonus, Company shares program and
Annual contribution to a fitness subscription.Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society.
It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem.
Requirements
- Previous experience in GDP and GMP regulated pharmaceutical / API industry
- Ability to identify non-compliance and gaps from quality standards
- Very good communication skills
- Strong team orientation
Benefits mentioned
- 5 weeks of vacation
- Employee referral bonus
- Company shares program
- Annual contribution to a fitness subscription
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