Gender: Female
Residence: Vaud, Switzerland
Short summary of skills, experience and career objective
PROFESSIONAL SUMMARY
Laboratory Technician with 4+ years of experience in GMP, GLP, biopharmaceutical, medical device, and research laboratory
environments, including Lonza and Integra LifeSciences. Proven in microbiological QC, environmental monitoring, cleanroom
operations, contamination control, sterile sampling, and GDP documentation - performing 250+ weekly microbiological
samples across 20+ cleanroom zones with zero critical deviations recorded. Skilled in Class A-D cleanrooms, Endotoxin/LAL
testing, HPLC basics, PCR basics, OOS/OOT deviation reporting, CAPA support, SOP documentation, sample preparation, and
trend analysis.
CAREER HIGHLIGHTS
• Maintained zero critical deviations across 250+ weekly microbiological samples (air, water, gas, surface) in sterile
production environments at Integra LifeSciences.
• Monitored 20+ cleanroom zones across Class A-D areas and hot flux zones, ensuring continuous GMP/GLP compliance
throughout production.
• Conducted 4 Endotoxin/LAL tests per month on water and disinfectants, with full OOS/OOT deviation reporting and CAPA
support.
• Installed and qualified Single-Use System filters and performed Filter Integrity Testing to confirm production readiness at
Lonza.
• Supported depyrogenation cycle validation and sterile condition checks during critical phases of medical device
production.
• Created and maintained SOPs and controlled documentation via Agile; managed inventory and material ordering through
Oracle.
PROFESSIONAL EXPERIENCE
Downstream Processing Operator (DSP) - LONZA AG
Visp, Switzerland | November 2025 - December 2025
• Executed GMP-compliant DSP workflows, including filtration, buffer handling, equipment preparation, and material flow in
controlled manufacturing areas.
• Performed environmental monitoring including air, surface, and swab sampling across cleanroom areas, ensuring accurate
GDP-compliant documentation.
• Installed and qualified Single-Use System filters and performed Filter Integrity Testing to confirm production readiness.
• Operated pumps, tubing assemblies, balances, and pH/conductivity meters; maintained Class A/B/C/D cleanroom
standards.
Laboratory Technician II - INTEGRA LIFESCIENCES
Le Locle, Switzerland | March 2025 - June 2025
• Conducted 250+ weekly microbiological samples (air, water, gas, surface) supporting sterile production environments with
zero critical deviations recorded.
• Monitored 20+ cleanroom zones and hot flux zones in compliance with GMP/GLP standards, flagging anomalies and
contributing to contamination trend investigations.
• Performed 4 Endotoxin/LAL tests per month on water and disinfectants; executed bacterial and fungal culture analysis and
microbial growth reporting.
• Reviewed HPLC contamination results and monitored temperature compliance for refrigerators, freezers, and incubators.
• Supported depyrogenation cycle validation and sterile condition checks during critical phases of medical device
production.
• Created and updated SOPs and controlled documentation via Agile; managed inventory and material ordering through
Oracle.
TECHNICAL SKILLS
QC Microbiology & Environmental Monitoring: Microbiological QC - Environmental Monitoring - Sterility Testing (swab) -
Endotoxin/LAL Testing (water/disinfectants) - Contamination Investigation - Trend Analysis
GMP / Quality Documentation: GMP Documentation - Deviation Reporting - OOS/OOT - CAPA Support - SOP Documentation -
GDP Compliance
Laboratory Techniques: Sample Preparation - HPLC Basics - PCR Basics - Cleanroom Operations (Class A-D) - Sterile Sampling -
Filter Integrity Testing - Single-Use Systems
Systems & Data Tools: EBRO - ELLAB - Agile - Oracle - DeltaV - Microsoft Excel - ImageJ
LANGUAGES
Italian (Native)
English (Fluent)
French (Proficient)
EDUCATION & CERTIFICATIONS
Bachelor of Science in Biology - Universita Degli Studi di Parma
Parma, Italy | Graduated 2022
• Relevant areas: microbiology, molecular biology, biotechnology, laboratory methods.
Professional profile
Career level:
Entry level
Status as medical specialist:
Laboratory monitoring
Medical specialty, field of interest:
Microbiology
Current (last) position held
Current employer company:
Lonza AG
Visp, Switzerland
Job title:
Downstream Processing Operator
Duration:
01 November 2025 - 31 December 2025
Work experience
Executed GMP-compliant DSP workflows, including filtration, buffer handling, equipment preparation, and material flow in
controlled manufacturing areas.
• Performed environmental monitoring including air, surface, and swab sampling across cleanroom areas, ensuring accurate
GDP-compliant documentation.
• Installed and qualified Single-Use System filters and performed Filter Integrity Testing to confirm production readiness.
• Operated pumps, tubing assemblies, balances, and pH/conductivity meters; maintained Class A/B/C/D cleanroom
standards.
Further work experience
Conducted 250+ weekly microbiological samples (air, water, gas, surface) supporting sterile production environments with
zero critical deviations recorded.
• Monitored 20+ cleanroom zones and hot flux zones in compliance with GMP/GLP standards, flagging anomalies and
contributing to contamination trend investigations.
• Performed 4 Endotoxin/LAL tests per month on water and disinfectants; executed bacterial and fungal culture analysis and
microbial growth reporting.
• Reviewed HPLC contamination results and monitored temperature compliance for refrigerators, freezers, and incubators.
• Supported depyrogenation cycle validation and sterile condition checks during critical phases of medical device
production.
• Created and updated SOPs and controlled documentation via Agile; managed inventory and material ordering through
Oracle.
Education and Qualifications
Language skills:
English: Excellent
Italian: Native
French: Excellent
German: Basic
Portuguese : Good
Special skills:
QC Microbiology & Environmental Monitoring: Microbiological QC - Environmental Monitoring - Sterility Testing (swab) -
Endotoxin/LAL Testing (water/disinfectants) - Contamination Investigation - Trend Analysis
GMP / Quality Documentation: GMP Documentation - Deviation Reporting - OOS/OOT - CAPA Support - SOP Documentation -
GDP Compliance
Laboratory Techniques: Sample Preparation - HPLC Basics - PCR Basics - Cleanroom Operations (Class A-D) - Sterile Sampling -
Filter Integrity Testing - Single-Use Systems
Systems & Data Tools: EBRO - ELLAB - Agile - Oracle - DeltaV - Microsoft Excel - ImageJ
Other qualifications
Laboratory Technician with 4+ years of experience in GMP, GLP, biopharmaceutical, medical device, and research laboratory
environments, including Lonza and Integra LifeSciences. Proven in microbiological QC, environmental monitoring, cleanroom
operations, contamination control, sterile sampling, and GDP documentation - performing 250+ weekly microbiological
samples across 20+ cleanroom zones with zero critical deviations recorded. Skilled in Class A-D cleanrooms, Endotoxin/LAL
testing, HPLC basics, PCR basics, OOS/OOT deviation reporting, CAPA support, SOP documentation, sample preparation, and
trend analysis.
Desired job profile
Desired job profile:
My ideal role would be a Laboratory Technician or QC Microbiology position within a GMP-regulated pharma, biotech, or medtech environment. I am particularly interested in hands-on laboratory work involving microbiological QC, environmental monitoring, cleanroom operations, contamination control, sample preparation, GMP/GDP documentation, and trend analysis.
I would be very interested in temporary or permanent opportunities, especially roles where I can contribute to reliable lab operations, quality compliance, and sterile production environments.
Desired job title:
Laboratory Technician | QC Microbiology | GMP & Cleanroom Operations
Type of position:
Laboratory position
Medical speciality:
Microbiology
Type of contract:
Permanent, Temporary/contract/project
Job status:
Full-time, Part-time
Years of relevant work:
1
Geographical preference:
Switzerland
Availability:
07 May 2026
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