Aktuell 14 English-Speaking Jobs in Blatten 3919 & Umgebung

KI-Beschreibung

In this role, you will oversee quality assurance operations for a growth project, ensuring compliance and timely delivery by coordinating 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
• •Fluent English (written & verbal) required

Deine Vorteile

KI-Beschreibung

In this role, you will lead impactful projects and drive technology changes across a global network, while mentoring scientists and influencing external forums to promote innovative capabilities.

• •10+ years of experience in upstream development in GMP environment
• •Advanced degree in chemical engineering, biotechnology, or related field
• •Proven track record in technology transfer and scale-up

Deine Vorteile

KI-Beschreibung

In this role, you will lead IT and OT infrastructure projects on a global scale, ensuring they meet established standards while collaborating with various teams. Your day-to-day responsibilities will include managing project lifecycles, budgets, and stakeholder communications to drive innovative solutions.

• •Proven experience in IT/OT infrastructure project management
• •Strong knowledge of IT and OT architecture, security, and compliance requirements
• •Familiarity with infrastructure topics such as servers, firewalls, LAN/WAN, and data centers

Deine Vorteile

KI-Beschreibung

In this role, you will focus on ensuring the successful validation of mammalian manufacturing processes, collaborating with various teams to meet regulatory standards and improve operational efficiency. Your day-to-day responsibilities will include planning validation activities, managing technical risks, and representing the organization in key meetings.

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

KI-Beschreibung

In this role, you will lead IT and OT infrastructure projects on a global scale, ensuring they meet established standards while collaborating with various teams. Your day-to-day responsibilities will include managing project lifecycles, budgets, and stakeholder communications.

• •Proven experience in IT/OT infrastructure project management
• •Strong knowledge of IT and OT architecture, security, and compliance requirements
• •Experience in Pharma or other validated production industries

Deine Vorteile

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 in a sterile environment.

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

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 or biology
• •Strong process understanding in Biopharma manufacturing
• •MS in Natural Science, Analytical Chemistry, Chemistry, or Biology

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

In this role, you will ensure that Environmental, Health, and Safety requirements are met throughout investment projects, from feasibility studies to detailed design. You will foster a strong EHS culture and conduct essential safety assessments.

• •EHS specialization in Process Safety or Fire Safety

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

You manage quality control processes, ensuring compliance with regulations and standards while overseeing testing, documentation, and method validation in partnership with contract laboratories.

• •Bachelor of Science
• •Minimum 9 years of experience
• •Excellent experience in managing CDMOs

Deine Vorteile

KI-Beschreibung

As a Trainee ERP Specialist, you will optimize ERP systems by managing part codes, developing BOMs, and ensuring compliance with SOPs. This role involves collaborating with teams to enhance processes and train others, making a significant impact on operational efficiency.

• •Degree or equivalent experience in Supply Chain Management or Business Management
• •Advanced experience in Supply Chain and Operations
• •Expertise in SAP Skills modules MM and PP