Job Description You will contribute directly to the establishment and validation of robust HPLC methods for complex biological molecules. Working in a GMP environment, you will collaborate closely with scientists and reviewers and ensure high‑quality analytical results for antibodies, proteins, and peptides. Your scientific expertise and customer‑focused mindset will strengthen our technical partnerships and help deliver reliable analytical solutions.
Responsibilities
Establishing HPLC methods in a GMP laboratory
Planning and conducting feasibility studies, method development and validation for antibodies, proteins, and peptides
Closely collaborating with laboratory staff, reviewers and other scientists
Writing and reviewing reports, validation documents and SOPs
Building trustworthy relationships with our customers and presenting results & findings
Qualifications
At least three years of professional experience in a GMP environment within the pharmaceutical industry required
Team player, who wants to share their knowledge with our team and improve their personal capabilities
Problem‑solving and solid interpersonal skills
Experience with High Performance Liquid Chromatography (HPLC)
Background in biochemistry, life sciences or a similar field
Experience in feasibility studies, method development and validations
Knowledge of software such as Chromeleon is an advantage
English fluency, German is an advantage
About Us Solvias is a global provider of chemistry, manufacturing, and control (CMC) analytics to the life sciences industry. Our expert team combines decades of experience with regulatory expertise across small molecules, biologics, and cell and gene therapies. Solvias offers end‑to‑end solutions from raw material testing to drug product release and API development for small molecules. Headquartered near Basel, Switzerland, Solvias operates six global Centers of Excellence, all adhering to the highest ISO, GMP, GLP, and FDA standards
#J-18808-Ljbffr
Responsibilities
Establishing HPLC methods in a GMP laboratory
Planning and conducting feasibility studies, method development and validation for antibodies, proteins, and peptides
Closely collaborating with laboratory staff, reviewers and other scientists
Writing and reviewing reports, validation documents and SOPs
Building trustworthy relationships with our customers and presenting results & findings
Qualifications
At least three years of professional experience in a GMP environment within the pharmaceutical industry required
Team player, who wants to share their knowledge with our team and improve their personal capabilities
Problem‑solving and solid interpersonal skills
Experience with High Performance Liquid Chromatography (HPLC)
Background in biochemistry, life sciences or a similar field
Experience in feasibility studies, method development and validations
Knowledge of software such as Chromeleon is an advantage
English fluency, German is an advantage
About Us Solvias is a global provider of chemistry, manufacturing, and control (CMC) analytics to the life sciences industry. Our expert team combines decades of experience with regulatory expertise across small molecules, biologics, and cell and gene therapies. Solvias offers end‑to‑end solutions from raw material testing to drug product release and API development for small molecules. Headquartered near Basel, Switzerland, Solvias operates six global Centers of Excellence, all adhering to the highest ISO, GMP, GLP, and FDA standards
#J-18808-Ljbffr
Scientist - Biological HPLC (m/f/d) 100% Arbeitgeber: Solvias
Solvias ist ein hervorragender Arbeitgeber, der seinen Mitarbeitern die Möglichkeit bietet, in einem dynamischen und innovativen Umfeld zu arbeiten. Mit einem starken Fokus auf Mitarbeiterentwicklung und einer offenen Unternehmenskultur fördern wir Teamarbeit und individuelle Entfaltung. Unsere zentrale Lage in der Nähe von Basel, Schweiz, ermöglicht es Ihnen, Teil eines globalen Netzwerks zu sein und an bedeutenden Projekten in der Pharma- und Biotech-Branche mitzuwirken.
