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Full-time
postgraduate degree
Posted 22d ago
~40 hrs/week
Responsibilities
Lead investigations, root cause analysis, and CAPA implementation for QC HPLC projects in a GMP environment. Responsible for the implementation, validation, and optimization of analytical methods while mentoring junior colleagues.
Requirements
Requires a Master's or PhD in chemistry, biochemistry, biology, or a related field with 5-10 years of pharmaceutical industry experience. Proficiency in GMP and experience with HPLC, CE, or icIEF is highly desired.
Full job description
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 people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
We are looking for a Scientist to join our QC HPLC Mammalian and mRNA team in Visp. Become part of our energetic and growing international team and take the opportunity to work on interesting projects in the rapidly developing field of Biologics.
Key responsibilities:
Investigation and management of deviations, as Lead Investigator
Root cause analysis (RCA) and CAPA implementation for project topics, and general lab topic.
Coaching and mentoring of junior QC colleagues.
QC analytical review and evaluation of results.
Technical writing and document review (test methods, APs, protocols, reports).
Quality oversight and audit readiness in GMP-regulated labs (participation in audits for assigned projects).
Support optimization of laboratory processes and workflows
Continuous improvement initiatives (Lean, 5S, Six Sigma, etc.)
Implementation, optimization, transfer and validation of analytical methods, with focus on HPLC, CE and icIEF.
Responsibility for all HPLC project related tasks and representation of HPLC team in the project team for the assigned projects.
Processing of investigations, change requests and deviations under cGMP.
Extraction and evaluation of analytical data, preparation of reports and presentations.
Preparation, review and approval of documents to ensure compliance with regulatory guidelines.
Expertise in analytical and technical issues for the assigned projects.
Key requirements:
Master or PhD in chemistry, biochemistry, biology or related field.
Minimum 5-10 years of proven experience in pharma industry.
Good understanding of GMP required.
Experience with HPLC, CE or icIEF desirable.
Ideally experience with IT systems like LIMS and CDS.
Proficient in English, German is a plus.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as meaningful as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a significant difference.
Related keywords
HPLCCEicIEFGMPLIMSCDSRoot Cause AnalysisCAPALean5SSix SigmaBiologicsMammalianmRNAAnalytical Method TransferQuality Control
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
How many Manufacturing jobs are open in Visp, Switzerland right now?
There are currently 120 open manufacturing positions in Visp, Switzerland listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Visp, Switzerland?
Companies currently hiring include Lonza, Arxada - NA Wood Protection Business Unit, Vaxcyte, ten23 health, Fusion Consulting, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Manufacturing jobs in Visp, Switzerland?
Yes — 11 of the 120 open manufacturing positions offer remote or hybrid work (0 remote, 11 hybrid).
How do I apply for Manufacturing jobs in Visp, Switzerland?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.