All jobsEngineeringChemical & Biomedical Engineering
8 Chemical & Biomedical Engineering Jobs in Switzerland
Problems move through the day as experiments run, batches process, and safety protocols shape every decision made.
Average salary: CHF 110,000
Average salary
CHF 110,000
across 6 jobs
- Bioprocess Engineer Cleaning Expert
- Lonza
- Visp, Switzerland
- CHF 90,000 – CHF 120,000New
- Laboratory Technician
- Qnity
- Meyrin, Switzerland
- CHF 65,000 – CHF 85,000New
- Lead Engineer Chemistry
- GE Vernova
- Baden, Switzerland
- CHF 120,000 – CHF 150,000New
- Lead Engineer Chemistry
- GE Vernova
- Baden, Switzerland
- CHF 100,000 – CHF 130,000New
- Process Systems Engineer (w/m/d)
- Endress+Hauser Group
- Reinach, Switzerland
- CHF 90,000 – CHF 120,000New
- Senior Chemical Engineer
- Exyte
- Basel, Switzerland
- CHF 110,000 – CHF 140,000New
- Validation & Compliance Engineer
- PerkinElmer
- Lucerne, Switzerland
- Validation & Compliance Engineer
- PerkinElmer
- Lucerne, Switzerland
Chemical and biomedical engineering roles involve designing, testing, and optimizing processes that manufacture pharmaceuticals, materials, and biologics. Work spans lab-scale development through large-scale production, often requiring hands-on troubleshooting alongside computational modeling. Employers typically seek candidates with degrees in chemical engineering, biomedical engineering, or chemistry, plus experience with process control systems, analytical instruments, and regulatory frameworks like GMP. Roles exist across pharmaceutical companies, contract manufacturers, food production facilities, and medical device firms, ranging from junior engineers supporting senior teams to process leads managing plant operations and regulatory compliance.
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Questions
What qualifications do entry-level roles require?
A bachelor's degree in chemical engineering, biomedical engineering, or chemistry is standard. Internship experience in manufacturing, quality assurance, or research labs strengthens applications, though some employers train graduates through structured rotational programs.
What does a typical day involve?
Days balance between lab work, data analysis, and meetings with cross-functional teams. Engineers might review batch records, troubleshoot equipment issues, design new experiments, or prepare documentation for regulatory submission depending on their project and seniority.
How much time is spent in the lab versus at a desk?
Distribution depends heavily on role and employer. Senior process engineers may spend 60% on analysis and planning; junior engineers often split time equally between lab testing, calculations, and documentation.
What technical skills matter most?
Proficiency with process simulation software, statistical analysis tools, and HPLC or chromatography instruments is common. Knowledge of manufacturing principles, scale-up methodology, and regulatory guidelines like FDA or ICH standards opens more opportunities.
How does this differ from research chemist work?
Biomedical and chemical engineers focus on making processes reliable, scalable, and compliant at production volumes. Research chemists emphasize discovery and synthesis; engineering roles solve how to manufacture consistently while meeting cost and quality targets.
What advancement paths exist?
Junior roles progress to senior engineer, then process lead or technical manager overseeing multiple projects or teams. Specialists may move into quality assurance, regulatory affairs, or plant engineering leadership depending on interests and certifications pursued.
How often does travel occur?
Travel varies significantly. Manufacturing site roles typically stay local; roles supporting multiple facilities or customer sites may travel monthly. Supply chain and quality roles often visit partner plants or attend regulatory audits.
What safety expectations shape the work?
Safety protocols are non-negotiable. Engineers follow strict procedures for hazardous chemicals, maintain cleanroom standards, and document all deviations. Regular training, incident reporting, and compliance audits are built into the rhythm of operations.
How much does regulatory compliance affect daily work?
Heavily. Documentation, batch records, change controls, and traceability are constant. Roles require attention to GMP standards, environmental regulations, and internal procedures; deviations trigger investigations and corrective actions.
What distinguishes this from chemical engineer roles in energy or materials?
Biomedical and pharmaceutical engineering prioritizes purity, potency, and regulatory validation over volume or cost alone. Work involves sterility assurance, stability testing, and patient safety considerations that differ fundamentally from commodity chemical or energy sector priorities.