48 marketing English-speaking jobs in Visp

Subject Matter Expert (SME) in environmental qualification, analytical testing, and product knowledge. Leads Environmental Monitoring (EM) performance qualifications (PQ) and ensures compliance with European GMP, ISO13485, and 21CFR820 standards.

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.

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.

Biotechnologist to support manufacturing operations in a clean room environment. Ensures safe, clean, and compliant production of liquid and freeze-dried drug forms. Collaborates with the manufacturing team to meet production needs while adhering to GMP standards.

Leads and executes equipment cleaning validation activities, including authoring and reviewing protocols and reports for COP, CIP, USP, DSP, and buffer/media systems. Supports SOP lifecycle for cleaning validation and coordinates with cross-functional teams on new or modified cleaning processes.

Program Management Analyst will translate data into informative views to support data-driven action. The role involves updating reporting and dashboards, supporting monthly revenue reconciliation, and leading projects to transform business management tools.

Associate Principal Scientist - Analytical Development will serve as the AD representative on pre-clinical project teams, coordinating with internal SMEs across all project phases. The role requires experience in protein analysis, physical-chemical methods, biochemical assays, and/or molecular biology techniques.

The End to End Program Leader will plan, manage, and execute the design, construction, commissioning, and validation of the throughput initiative for Integrated Biologics, Mammalian Operations 1k2k Visp. The role requires a Master's degree in a relevant field and 10+ years of experience in Manufacturing/Operations.

Bioprocess Engineer needed for clinical and commercial manufacturing of life-saving therapies. Lead preparation, execution, cleaning, and changeover in assigned area. Master's Degree or equivalent experience in Biotechnology, Biochemical Engineering, Biochemistry, or related field required. Knowledge of USP or DSP units and GMP experience necessary. Excellent communication skills in English.

As a QA Specialist, you will strengthen data-driven quality oversight within environmental and utility monitoring. You will author GMP-compliant EM reports, support batch release reviews, and lead complex investigations. You will present monitoring performance and contribute to continuous improvement initiatives.

Leads a team responsible for deviation investigation, CAPA management, and ensuring cGMP compliance. Manages team performance, investigates deviations, and collaborates with stakeholders to improve processes and meet production schedules.

Lead and develop a high-performing operations team, ensuring timely project delivery and high quality standards. Plan workloads, serve as a point of contact for stakeholders, and support operational strategy development.

This role focuses on connecting data, processes, and people to unlock operational performance in manufacturing. The Process Analytics & Operational Data Intelligence Expert will build analytics-ready datasets, analyze process trends, and develop solutions to improve operational performance.

Manage material processes in module L to ensure timely availability for production. Collaborate with manufacturing and supply chain teams to optimize material use and meet production needs.

Manages a team of 6x20k DSP production staff, overseeing safety, quality, and on-time delivery. Collaborates with the Head of DSP on production planning, problem-solving, and innovation projects. Responsible for shift team performance, safety culture, training, and long-term planning.

Senior Program Manager responsible for leading complex programs from contract signature to delivery. Manages cross-functional teams, ensures on-time and on-budget project completion, and acts as the customer advocate. Requires a Bachelor's or Master's degree in a relevant field, multi-year project management experience, and strong communication and leadership skills. Fluency in English is required, German is a plus.

Perform analytical methods in QC biochemistry, including ELISA and qPCR, ensuring compliance with GMP and safety regulations. Support method implementation, validation, and transfer activities. Contribute to process improvement and daily laboratory operations.

Supply Chain Project Team E2E Lead will bridge the gap between clients and internal teams to ensure flawless operational execution. The role requires strong analytical abilities, presentation skills, and experience in supply chain management, ideally within Pharma or CDMO.

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.

Executes manufacturing activities in Drug Product according to cGMP guidelines. Ensures batch execution, evaluates test results, and resolves issues. Provides technical and procedural support to the manufacturing team. Responsible for production documentation and supports process investigations and CAPAs. Requires 2-4 years of experience in a GMP environment and fluency in English or German.