Validation Expert - Drug Product Process Validation; temporary
Listed on 2026-07-19
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Pharmaceutical
Quality Engineering, Regulatory Compliance Specialist
Location: Kaiseraugst
Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir.
Rejoignez Roche, où chaque voix compte.
At the Kaiseraugst site, around 1,800 employees with an innovative spirit and the highest quality standards ensure the continuous supply of medicines to patients worldwide. As part of Pharma Technical Operations (PT), the site is a central pillar of sterile drug product manufacturing MSAT Sterile Team (Manufacturing Science and Technology) actively shapes the technological advancement, validation, and optimization of aseptic processes, combining scientific expertise with GMP compliance to ensure safe, efficient, and sustainable manufacturing processes for sterile drug products.
TheOpportunity
As a Validation Expert - Drug Product Process Validation, you will be responsible for the design, execution, and GMP-compliant documentation of product-independent process validations within sterile drug product manufacturing. Working at the interface of Production, Engineering, Quality Assurance, and global network partners, you will make a decisive contribution to process safety and inspection readiness while shaping technical concepts, strategic network initiatives, and validation standards.
Process Validation Execution
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Design, plan, execute, and evaluate product-independent validation studies (e.g., Visual Inspection, Autoclaving, Sterilization-in-Place (SIP), Sterile Hold Time (SHT), and Crimping), including sample management, shipping, and GMP-compliant documentation.Technical Evaluations
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Conduct technical assessments, root cause analyses, and prepare Quality Impact Assessments to ensure continuous process safety and quality.Project & Process Lifecycle
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Manage or collaborate on local and cross-site validation projects, process improvements, and clinical Phase 3 manufacturing.Cross-Functional Collaboration
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Partner closely with Kaiseraugst Manufacturing Units (Antibiotics & Sterile Filling), Engineering, Quality Assurance, and global network stakeholders.Global Network & Benchmarking
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Discuss and benchmark validation concepts with Pharma Technical Development, and represent the department in huddles, steering, and planning meetings.Audit & Compliance Support
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Ensure validation activities align with PQS and regulatory requirements, supporting health authority inspections, internal audits, and regulatory dossier preparation.Technical Impact & Visibility
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Take on a high-visibility, interdisciplinary role with access to global know-how and digital tools, directly contributing to the safety and quality of life-saving medicines.
Education & Professional Experience
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Completed degree in pharmacy, natural sciences, engineering, or a comparable qualification, paired with several years of professional experience.Validation & GMP Expertise
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Proven experience in planning, executing, and evaluating validation studies in a GMP environment, alongside a solid knowledge of sterile manufacturing processes.Communication & Collaboration
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Excellent written and verbal communication skills in both German and English, with a strong ability to collaborate cross-functionally within a global network.Analytical & Proactive Mindset
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High level of initiative, systematic thinking, and a solution-oriented working style, with a readiness to adapt to and actively shape new technologies and processes.Passion for Improvement
: A strong willingness to learn, a passion for innovation, and an affinity for continuous improvement principles (Lean Thinking, LPS).
Ready to take the next step? We'd love to hear from you. Apply now to explore this exciting opportunity!
Qui nous sommesUn avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique.
Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial.
Construisons ensemble un avenir plus sain.
Roche est un employeur offrant l'équité en matière d'emploi.
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