103 centre de formationpour les cha English-speaking jobs in Canton of Valais

Analytical Scientist to support method validation, verification, and transfer for clinical development products. Requires 5+ years of pharmaceutical industry experience, GMP environment, and strong analytical method expertise.

Senior QA Specialist will own quality responsibilities for biopharmaceutical manufacturing processes. Responsibilities include reviewing and releasing records, assessing product changes, investigating deviations, and training junior employees. Requires a degree in a related field, experience in the GMP regulated pharmaceutical industry, and strong communication skills.

Provides support for material management in microbial cGMP manufacturing processes. Assists with material quality issues, single use assembly design and qualification, and process troubleshooting. Collaborates with cross-functional teams to ensure robust and compliant processes. Requires a Bachelor's or Master's degree in a relevant scientific discipline and strong interest in microbial manufacturing.

The Reservations Supervisor assists in the efficient operation of the Reservations department to provide exceptional products and services. Responsibilities include supervising Reservations hosts, ensuring adherence to policies and procedures, and overseeing the smooth operation of the department. The role requires a thorough knowledge of resort facilities, services, rates, and reservation procedures. The Supervisor will also assist in training, performance reviews, and resolving guest complaints.

Lead and support SAP EWM implementations and enhancements for pharmaceutical operations. Configure and optimize SAP EWM processes, ensuring compliance with industry standards.

Lab Analytical Scientist to support analytical activities for clinical development and process validation stage products. Focus on method suitability assessment, validation, verification, and transfer in alignment with GMP ICH guidelines. Requires expertise in physical and chemical technologies.

Coordinate and support downstream production activities across various departments to ensure timely and compliant execution. Lead workforce planning, training, and performance management for DSP production support. Manage recruitment and onboarding of production personnel.

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.

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

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.

Senior QA Specialist ensures compliance with GxP standards, corporate policies, and regulatory guidelines. Supports QA operations, audits, and implements Lean/OPEX approaches. Requires a Life Science degree, experience in a regulated environment, and fluency in English.

Associate Director leads the development and implementation of asset and technology solutions for growth projects. Focuses on cost-effective, compliant, and reliable manufacturing by design. Drives innovation initiatives, evaluates solutions, and optimizes operational expenditure and asset lifecycle costs.

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.

As In Room Dining Host, you will deliver exceptional guest experiences while embodying Six Senses' vision and values. You will ensure efficient service, uphold sustainability practices, and contribute to creating memorable "Out of the Ordinary" moments.

Reviews executed batch records to ensure compliance with procedures and regulations. Tracks and reports review activities to support timely batch releases. Collaborates with Operations to ensure manufacturing documentation meets GMP standards.

Electrical Instrumentation & Control Technician will perform maintenance and calibration activities for electrical, measurement, and control systems. Responsibilities include troubleshooting malfunctions, documenting work, ensuring compliance with regulations, and collaborating with teams to improve equipment performance. Requires experience in pharmaceutical or biotech industry, proficiency in relevant software, and familiarity with GMP standards.

Investor Relations Intern will research, map, and outreach to capital allocators including family offices, institutional investors, and high-net-worth individuals. Interns will assist in developing outreach strategies, investor communications, and presentation materials.

The Capex Buyer supports the execution of capital expenditure procurement activities within assigned projects. Responsibilities include operational buying, supplier coordination, and compliance with procurement processes. The role requires a Bachelor's degree or equivalent experience in a related field and initial experience in procurement, supply chain, or operational buying.

CSV Engineer responsible for the validation of computerized systems on process engineering equipment and facilities. Prepares commissioning and validation documents, supervises deviations and changes, and coordinates CSV executions with internal and external groups. Requires a Bachelor's/Master's degree in a technical field and significant experience in CSV within a regulated environment.

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.