QA Validation Specialist

QA Validation Specialist ?? QA Validation Specialist 1 year temporary mission Are you passionate about quality, scientific rigor, and innovation in the life sciences? Join a dynamic team where your expertise will directly contribute to ensuring the compliance and performance of critical GMP equipment, facilities, and systems. ?? Your Mission As a QA Validation Specialist, you play a key role in maintaining a compliant, safe, and high-performing manufacturing environment. You will ensure that all equipment, facilities, and systems remain in a validated state, aligned with user requirements, process parameters, and global regulatory standards. ?? Key Responsibilities Provide QA oversight for validation and qualification activities to ensure GMP compliance. Conduct change control assessments and ensure alignment with regulatory expectations. Develop and review validation protocols (IQ, autoclaves, clean utilities, shipping validation, temperature mapping, etc.). Collaborate closely with Operations, Quality Assurance, clients, and regulatory bodies. Offer technical expertise in reviewing and approving SOPs, protocols, reports, deviations, CAPAs, and change controls. Manage quality systems such as DMS, LIMS, Kneat, and Trackwise. Mentor junior team members and coordinate tasks in collaboration with the Validation Manager. ?? Your Profile Bachelor’s degree in a scientific or technical field. 2–6 years of experience in the pharmaceutical industry. Solid understanding of cell and gene therapy manufacturing equipment and validation processes is a plus. Strong analytical mindset, attention to detail, and a collaborative spirit. Fluent in English jid2e23c27afr jit0727afr

Location: Visp, 3930, CH

Posted Date: 7/3/2025