39 English-speaking jobs in Visp

Support process validation across Upstream and Downstream operations. Assist in drafting, reviewing, and executing validation protocols and reports. Requires a university student in a relevant field with strong analytical and teamwork skills.

Lead Drug Linker Development and PD/MSAT/DSP Chemists, driving pipeline optimization and unit setup. Requires PhD in Chemistry/Engineering and 5-10 years in pharma process development.

DeltaV Automation Engineer needed for high-automated Biologics facilities. Responsibilities include planning MSR readiness, ensuring DeltaV/MES operation, and managing GMP activities. Requires relevant engineering experience and proficiency in SAP, COMOS, and DeltaV is desirable.

Intern in QC Bioanalytics supporting biochemical analyses in a GMP-regulated laboratory. Tasks include routine ELISA and qPCR analysis, method implementation, and administrative support. Requires relevant training or a Bachelor's degree.

Lead MES DeltaV projects across the full lifecycle, strengthening system standards, and ensuring GMP-compliant performance. Requires a degree in a related field and experience in IT/OT or MES DeltaV within a regulated environment.

CSV Engineer for Biologics responsible for generating and executing computerized system validation on process engineering equipment. Duties include preparing validation documents, supervising projects, and ensuring adherence to protocols.

Drive new business and expand relationships for Drug Product Services across EMEA. Requires experience in aseptic filling and fill-finish services, biologics, or CDMO sales.

Own and execute the monthly Supply Planning cycle for Microbial operations, improving the Supply Plan, MPS, and capacity outlook. Requires experience in Supply Planning, S&OP, and SAP IBP/ECC.

Operator/Biotechnologist role involves manufacturing biopharmaceutical products while ensuring cGMP compliance. Responsibilities include executing production operations, investigating deviations, and collaborating with cross-functional teams. Education in life sciences is required.

Senior CAPEX Planner Controller develops and manages integrated project schedules for large capital projects. Requires 5-10 years of experience, strong Primavera P6 skills, and essential experience in the pharmaceutical industry.

Ensure critical GMP processes are validated and maintained in compliance with global regulatory guidelines. Oversee validation activities for biotechnological manufacturing, manage CPV, and act as a QA point of contact for product transfer.

Internship supporting large-scale mammalian upstream and downstream manufacturing. Tasks include documentation, data analysis, and process improvement initiatives. Requires a degree in Biotechnology, Chemical Engineering, or related field.

Experienced Chemist/Chemical Engineer needed for Small Molecule Lead Chemist role focusing on DSP and preparative chromatography. Drive DSP technology improvement, lead process development, and support strategic growth. PhD required.

QA Manager in QA Analytics ensures QC processes comply with GxP, data integrity, and regulatory standards. This role involves representing QA in cross-functional teams, reviewing QC documents, and driving CAPA.

Support upstream or downstream biopharmaceutical manufacturing activities in compliance with cGMP. Troubleshoot equipment, maintain documentation, and support quality initiatives. Requires a background in life sciences and experience in biopharma manufacturing.

Project Engineer needed for freelance/contracting role in Visp. Define technical requirements, manage project roadmap, and ensure GMP compliance. Experience in biopharmaceutical manufacturing, project management, and CQV activities required.

Head of Plant Engineering leads engineering operations, maintenance strategy, utilities, and capital investments across manufacturing plants. Requires 10+ years in engineering leadership, strong GMP knowledge, and business-fluent English.

Senior Bioprocess Engineer specializing in Downstream Processing (DSP) for GMP biomanufacturing. Provide technical leadership, hands-on support, and drive process improvements in purification operations. Requires 10+ years of relevant experience.

Lead procurement activities for assigned portfolios, ensuring supply continuity and cost competitiveness. Manage supplier relationships, drive SRM initiatives, and oversee vendor performance. Requires SCM/Procurement experience and SAP MM knowledge.