402 English-speaking jobs in Canton of Valais

QA Raw Material Compliance Specialist supports the management of Vendor Change Notifications (VCNs) ensuring compliant and controlled implementation. Requires 5+ years experience in QA, Supplier Management, Change Control, or GMP support, strong understanding of GMP regulations, and extensive TrackWise experience.

QA Raw Material Compliance Specialist ensures raw material quality and compliance by managing Vendor Change Notifications (VCNs). This role involves reviewing, assessing, and coordinating VCN evaluations, conducting impact assessments, and tracking VCNs to ensure adherence to procedures and regulations.

Teamlead for Downstream Production, coordinating and supporting activities across various production stages. Leads workforce planning, training, performance management, and team development. Requires a Bachelor's or Master's degree in a relevant field or equivalent experience in large-scale DSP production. Strong GMP experience and leadership skills are essential.

Drive digitalization of operational workflows and support process improvements in a manufacturing environment. Apply Operational Excellence principles to identify and implement improvements.

QA Project Manager will establish Quality Agreements, act as QA representative in project teams, and manage customer interactions. Requires a university degree in a relevant field and long-term GMP experience in the pharmaceutical industry.

Reviews, assesses, and coordinates Vendor Change Notifications (VCNs) ensuring compliance with GMP requirements and internal procedures. Manages VCNs, tracks documentation changes, and collaborates with stakeholders. Requires a Bachelor's or Master's degree in a scientific discipline and 5+ years of experience in QA, Supplier Management, or Change Control.

QA Raw Material Compliance Specialist ensures raw material quality and compliance by managing Vendor Change Notifications (VCNs). This role involves reviewing, assessing, and coordinating VCN evaluations, conducting impact assessments, and tracking VCNs to ensure adherence to procedures and regulations.

As Housekeeping Runner Attendant, you will support the efficient operation of housekeeping, ensuring linen par levels, collecting supplies, and assisting Room Attendants. You will also handle guest requests, report issues, and maintain hygiene standards.

Physchem Lab Analytical Scientist supports analytical activities for clinical development products. Focus on method suitability assessment/validation/verification/transfer per GMP, ICH guidelines, and company quality system. Requires 5+ years of pharma industry/GMP experience, Bachelor's degree, and fluency in English. German is a plus.

As Housekeeping Runner Attendant, you will support the efficient operation of housekeeping, ensuring linen par levels, collecting supplies, and assisting Room Attendants. You will also handle guest requests, report issues, and maintain hygiene standards.

The Batch Record Review Intern supports the Quality Assurance team by reviewing, verifying, and organizing electronic GMP manufacturing documentation. This role involves reviewing executed batch records, clarifying comments, and supporting deviation and investigation processes.

Provides site support as part of the QA supplier management team. Reviews, evaluates, and coordinates supplier change notifications, ensuring compliance with GMP regulations.

Analytical Scientist to support clinical development, focusing on method suitability assessment/validation/verification/transfer. Requires 5+ years of pharma industry/GMP experience, Bachelor's degree, and fluency in English.

The Social District of La Castalie seeks an 80% Unit Manager to organize, manage, and develop three accommodation structures for adults with intellectual and/or multiple disabilities.

Lead Expeditor needed to ensure timely delivery of materials and maintain efficient procurement processes. Coordinate with suppliers, manage reporting systems, and support internal stakeholders to meet KPIs. Requires strong organizational and communication skills, proficiency in Microsoft Office, and experience in data analytics and reporting. Must be fluent in English and have relevant experience in a similar role. Flexibility to work 3 days on-site (Visp or Stein) and 2 days remotely.

Expediter to ensure timely material delivery and maintain efficient procurement processes. Coordinate with suppliers, manage reporting systems, and support internal stakeholders to meet KPIs. Requires strong organizational and communication skills, proficiency in Microsoft Office, and experience in data analytics. Must be fluent in English and have relevant experience in a similar role. This is a hybrid position with 3 days on-site (Visp or Stein) and 2 days remote.

This GMP Hygiene & Cleanroom Project Lead role involves implementing and improving hygiene standards at the Visp site. Responsibilities include leading projects, performing Cleanroom Performance Qualifications, and preparing hygiene-related documentation. The ideal candidate has a scientific background, GMP experience, and strong communication and analytical skills.

This temporary role (10 months) in Visp, Switzerland, focuses on implementing and improving hygiene standards at a pharmaceutical site. The Central Hygiene Project Manager will lead projects, conduct cleanroom performance qualifications, and manage documentation. The ideal candidate has a scientific background, GMP experience, and strong communication skills.

Lab Analytical Scientist needed to support analytical activities for clinical development and process validation. Focus on method suitability assessment, validation, verification, and transfer. Requires expertise in physical and chemical technologies, pharmacopeia requirements, and global alignment. Full-time, on-site presence required.

QA Raw Material Compliance Specialist will support the management of Vendor Change Notifications (VCNs) ensuring compliant and controlled implementation. Responsibilities include reviewing, assessing, and coordinating VCNs, completing impact assessments, and managing VCNs according to GMP requirements.