65 English-speaking jobs in Visp

Lead cross-functional teams as a Process Expert MSAT Downstream for Mammalian Large Scale. Responsibilities include technology transfers, process implementation, and ensuring process scalability while managing GMP risks.

Senior QA Specialist supports quality management system oversight. Responsibilities include generating compliance reports, supporting document implementation, and participating in audits. Requires GMP experience in "Drug Products" and customer complaint management.

Experienced MSAT Chemist needed to support HPAPI processes in production facilities. Key duties include process transfer support, troubleshooting, and serving as a subject matter expert in preparative chromatography. Requires a Chemistry degree and 2+ years of preparative chromatography experience.

Associate Principal Scientist to lead upstream process development in Mammalian Cell Culture. Responsibilities include executing complex studies, serving as CHO cell culture SME, and optimizing scale-up/down models. Requires relevant industry experience.

Senior QA Specialist for Bioconjugates supports continuous improvement and manages quality systems. Responsibilities include reviewing SOPs, managing deviations, and acting as a QA SME in audits. Requires a degree in a life science field and GMP experience.

Material Planner supports site supply chain operations by ensuring timely material availability for production. Responsibilities include converting planned orders, managing material plans, processing purchase requisitions, and optimizing inventory. Proficiency in MRP systems and analytical tools is required.

Material Planner role focusing on MRP, Purchase Order Management, and Expediting within Life Sciences supply chain operations. Requires experience with SAP MM and inventory optimization.

Operations Planner responsible for comprehensive operations planning in Manufacturing Complex 2. Duties include shop floor scheduling, coordinating resources and materials, and developing the Summary Production Schedule. Requires supply chain or biotechnology degree.

Bioprocess Engineer manages operational activities for manufacturing projects, standardizing Up Stream equipment at Manufacturing Complex 2. Requires BSC/MSc plus 5/3 years in biotech, expertise in mammalian cell culture, and experience with stainless steel/Single Use Systems.

Intern to support day-to-day QC activities within the QC HPLC Mammalian team. Responsibilities include performing lab activities under GxP, documenting data, and supporting project scientists. Requires a Bachelor's degree in a relevant science and proficiency in English.

HR Generalist for a project role. Support HR Business Partners in operational and strategic activities, managing the full employee lifecycle. Requires HR education, generalist experience, and strong communication skills.

HR Generalist supporting operational and strategic HR activities. Responsibilities include advising on HR processes, managing the full employee lifecycle, and contributing to talent management and organizational change. Requires HR experience and knowledge of employee lifecycle processes.

The Ops Scheduler performs holistic operations planning for mid-scale upstream and downstream production, ensuring safety and on-time delivery. Requires several years of experience in pharmaceutical supply or project planning.

Support the site's Data Integrity program at a large biologics manufacturing site. Promote ALCOA+ principles, support governance, and coordinate DI assessments across GMP processes. Requires relevant degree and GMP experience.

DeltaV Automation Engineer role involves planning and realizing electrical MSR readiness and ensuring seamless operation of high-automated Biologics facilities using DeltaV and MES systems. Requires engineering experience and proficiency in SAP, COMOS, and DeltaV.

Review analytical data from HPLC and CE analyses to ensure GMP compliance and support monoclonal antibody batch release. Requires a BSc/MSc in a related field and strong attention to detail.

Process Expert MSAT is responsible for successful transfer, scale-up, supervision, and optimization of mammalian cell culture processes. This role involves leading cross-functional teams and acting as a process owner. A degree and 5+ years of biopharma manufacturing experience are required.

PMO Lead to design and implement the PMO Target Operating Model. Responsibilities include establishing project governance, portfolio management frameworks, and implementing planning and control processes. Requires strong experience in PMO design and portfolio management.

PMO Lead to design and implement the PMO Target Operating Model. Responsibilities include establishing project governance, portfolio planning, and implementing performance management processes. Requires strong experience in PMO setup and portfolio management.

MSAT Process Specialist supports biopharmaceutical manufacturing by overseeing process validation, scale-up, and continuous improvement. Requires 3-5 years in process development with a degree in a related scientific discipline.