QC Analyst / Data Reviewer — Lonza
- Location
- Visp
- Contract
- full-time
- Posted
- 8 days ago
Role overview
Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is dedicated individuals working together, brainstorming ideas that support businesses in making a positive impact on society.
- Today, Lonza is a global leader in life sciences operating across three continents.
- While we work in science, there’s no magic formula to how we do it.
- Your primary responsibilities will revolve around conducting routine analysis of biopharmaceuticals using HPLC and capillary electrophoresis techniques.
- In this role, you will also be responsible for reviewing data generated during routine Quality Control (QC) analysis in the QC Laboratory.
- in Visp What you will do:
- You review HPLC data and other laboratory-related raw data to ensure accuracy, completeness, and compliance.
Main responsibilities
- Your primary responsibilities will revolve around conducting routine analysis of biopharmaceuticals using HPLC and capillary electrophoresis techniques.
- In this role, you will also be responsible for reviewing data generated during routine Quality Control (QC) analysis in the QC Laboratory.
- Your expertise will ensure that all laboratory work aligns with GMP and SOPs, enabling the timely release of monoclonal antibody batches. What you will get:
- An agile scientific career in a dynamic, GMP‑regulated environment.
- An inclusive and ethical workplace that values collaboration and accountability.
- Compensation programs that recognize performance and technical expertise.
- Opportunities to deepen your expertise and take ownership of impactful projects.
- Exposure to cross‑functional collaboration and regulatory interactions.
- A supportive culture that encourages continuous improvement and learning.
- Competitive local benefits.
What the company offers
- in Visp What you will do:
- You review HPLC data and other laboratory-related raw data to ensure accuracy, completeness, and compliance.
- You perform tasks within the gLIMS laboratory execution system, including creating consumable types and managing instruments and consumables.
- You ensure all activities comply with GMP requirements and internal procedures.
- You investigate ambiguous results with curiosity and attention to detail.
- You adapt effectively to changing priorities in a dynamic Quality Control environment. What we are looking for:
- You have completed training as a laboratory technician or hold a bachelor’s degree in chemistry, biochemistry, or a related scientific field.
- Experience in a GMP-regulated Quality Control environment is highly preferred.
- Hands-on experience with HPLC and/or capillary electrophoresis (CE) is preferred.
- You bring a highly detail-oriented, flexible, and investigative mindset. You communicate fluently in English;
Application process
- now.
- Lonza is a global leader in pharma and biotech manufacturing.
- The company operates major production facilities in Visp (Valais), Basel, and Stein (Aargau), Switzerland.
Additional details
- Your expertise will ensure that all laboratory work aligns with GMP and SOPs, enabling the timely release of monoclonal antibody batches.
- You adapt effectively to changing priorities in a dynamic Quality Control environment. What we are looking for:
- You bring a highly detail-oriented, flexible, and investigative mindset. You communicate fluently in English;
- German skills are a plus.
Notes and original content
- What you will get:
- Benefits in Visp
- What you will do:
- You adapt effectively to changing priorities in a dynamic Quality Control environment.
- What we are looking for:
- You bring a highly detail-oriented, flexible, and investigative mindset.
- You communicate fluently in English;
- About Lonza
Questions about this listing
What salary does Lonza offer for this role?
Lonza lists CHF 60'500 - 91'500 gross per year for this position in Visp. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Lonza offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Lonza during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Valais?
EU/EFTA residents living in the border zone of the country adjoining Canton Valais can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Valais's cantonal migration office or with HR during the application.
How do I apply for this position at Lonza?
Use the "Apply now" button on this page — it links directly to Lonza's original listing at lonza.wd3.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
