140+ English-Speaking Jobs in St. Niklaus

KI-Beschreibung

As a QA Manufacturing Specialist, you will ensure product quality by monitoring manufacturing processes, conducting audits, and providing on-the-floor training. This role involves real-time oversight, documentation review, and supporting compliance with GMP standards.

• •Strong background in quality assurance within pharmaceutical or regulated manufacturing environment
• •Solid understanding of GMP (Good Manufacturing Practices)
• •Good understanding of aseptic process and its core requirements

Deine Vorteile

KI-Beschreibung

In this role, you will lead the evolution of Quality Management Systems while ensuring compliance with global regulations. Your day-to-day responsibilities will involve driving cultural transformation, mentoring teams, and collaborating across departments to uphold stringent quality standards.

• •Proven experience in a GMP-regulated environment
• •Leadership in building, optimizing, or remediating Quality Management Systems (QMS)
• •Strong track record managing end-to-end quality processes

Deine Vorteile

KI-Beschreibung

In this QA internship, you will engage in various quality assurance activities, ensuring compliance with standards while collaborating with teams to enhance production and documentation processes.

• •Enrollment in or completion of Bachelors or Masters in Pharmacy, Pharmaceutical Sciences, Biotechnology, Biochemistry, Biology, or related field
• •Fluency in written and spoken English
• •Prior experience in a research laboratory environment

KI-Beschreibung

In this role, you will support the Project Director in managing large investment projects from design to handover. Your day-to-day responsibilities will include organizing workshops, preparing reports, and enhancing project structures to ensure smooth operations.

• •Diploma, Master's, or Bachelor's in project management, engineering, mechanical, chemical, or related field
• •Technical knowledge in chemical or pharmaceutical engineering
• •Experience in SharePoint or website management

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KI-Beschreibung

In this role, you will manage IT and OT systems in a regulated pharmaceutical environment, ensuring compliance and reliability. You will collaborate with various teams to troubleshoot issues and drive continuous improvement.

• •Bachelor's degree in a corresponding field
• •X years of experience
• •Pharma/GMP experience preferred

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KI-Beschreibung

In this role, you will be at the forefront of integrating and optimizing MES data within logistics operations. Daily tasks will involve leading automation projects, troubleshooting issues, and collaborating with various teams to enhance efficiency and drive digital transformation.

• •Bachelor degree in a corresponding field
• •SAP knowledge mandatory
• •X years of experience

Deine Vorteile

KI-Beschreibung

In this internship, you will engage in hands-on lab work with advanced techniques while collaborating with a team of scientists. You will also have the chance to lead improvement projects and contribute to training efforts, all within a well-maintained and organized lab environment.

• •MSc or BSc specializing in biology, biochemistry, or a similar field
• •Good knowledge of English
• •Team player and well organized

KI-Beschreibung

In this role, you will focus on organizing sample storage, preparing and packaging samples, and ensuring accurate documentation. Your day-to-day responsibilities will involve maintaining inventory and managing tasks in software systems, all while adhering to GMP standards.

• •Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related field
• •Experience in a laboratory or regulated environment
• •Proficiency with laboratory software and documentation practices

Deine Vorteile

KI-Beschreibung

In this role, you will oversee quality assurance operations for a growth project, ensuring compliance and timely delivery by collaborating with various departments and making informed decisions on the manufacturing floor.

• •Significant experience in pharmaceutical Quality area
• •Work experience in Quality Assurance, Production or Engineering in pharmaceutical industries and cGMP regulated environment
• •Excellent knowledge of computer systems and quality tools such as risk based approaches

Deine Vorteile

KI-Beschreibung

In this role, you will focus on ensuring the successful validation of mammalian manufacturing processes. You will collaborate with various teams to manage technical risks and maintain compliance while actively participating in audits and continuous improvement initiatives.

• •Minimum 1 year of experience in process validation within a cGMP-regulated biopharmaceutical environment
• •Proven experience in managing complex projects
• •Bachelor’s, Master’s or PhD degree in biotechnology, chemical engineering or related disciplines

KI-Beschreibung

In this role, you will lead a dynamic team focused on process validation for mammalian manufacturing. Your day-to-day responsibilities will include managing validation activities, collaborating with cross-functional teams, and ensuring compliance with regulatory standards.

• •Minimum 5 years of experience in process validation within a cGMP-regulated biopharmaceutical environment
• •Bachelor’s, Master’s or PhD degree in biotechnology, chemical engineering or related disciplines
• •Proven leadership experience in managing technical teams and complex projects

KI-Beschreibung

In this role, you will be at the forefront of drug product manufacturing, ensuring compliance with cGMP while troubleshooting issues and supporting the team. Your day-to-day responsibilities will involve operating equipment, training staff, and maintaining high standards of quality.

• •2-4 years of experience in GMP environment on the shopfloor or completed EFZ apprenticeship as a mechanic or related profession
• •Proficiency in English
• •Familiarity with GMP requirements, quality procedures, and SOP execution

Deine Vorteile

KI-Beschreibung

In this role, you will focus on validating mammalian manufacturing processes, ensuring compliance with regulatory standards, and collaborating with various teams. Your expertise will be vital in managing technical risks and enhancing process efficiency.

• •Minimum 1 year of experience in process validation within a cGMP-regulated biopharmaceutical environment
• •Proven experience in managing complex projects
• •Bachelor’s, Master’s or PhD degree in biotechnology, chemical engineering or related disciplines

KI-Beschreibung

In this role, you will focus on assessing workplace health hazards and conducting exposure monitoring. You will also deliver training to promote safe practices, maintain exposure data, and collaborate with teams to ensure compliance and improve health protection.

• •Minimum 5 years of experience in analytical chemistry, biology, or chemical/biological production
• •MS in Natural Science, Analytical Chemistry, Chemistry, or Biology
• •Strong process understanding in Biopharma manufacturing, cGMP, safety, and biosafety compliance

Deine Vorteile

KI-Beschreibung

In this leadership role, you will shape global regulatory strategies for vaccine development, guide cross-functional teams, and ensure compliance with regulatory requirements while interacting with authorities to expedite approvals.

• •15+ years industry experience demonstrating technical and regulatory expertise
• •10+ years of extensive and relevant regulatory experience
• •Direct experience engaging multiple health authorities

Deine Vorteile

KI-Beschreibung

You will lead the development of materials and chemical processes while managing laboratory work and data analysis. Building customer relationships and mentoring lab technicians are also essential aspects of this role.

• •Advanced degree in material science
• •Significant knowledge of material characterization
• •Enjoy experimental work in the laboratory

KI-Beschreibung

As a Junior Quality Engineer, you will engage in a variety of tasks, including conducting inspections and audits, as well as supporting quality improvement initiatives. This role focuses on optimizing processes and ensuring compliance with safety and quality standards.

• •Bachelor’s degree or equivalent combination of education and relevant experience
• •Experience in quality assurance, manufacturing, or process engineering
• •Strong analytical, problem-solving, and data-interpretation skills

Deine Vorteile