9 process manager emplois trouvés à Vaud.

For our client, we are seeking a Process Specialist to coordinate and execute site activities within the MSAT (Manufacturing Science and Technology) department.Your Role :Coordinate with the project stakeholders the site activities for new product introductions, technology transfer (TT), validation of processes or process changes for commercial products. Ensure coordination of production activities on the shop floor falling under your

Vous êtes expert·e en procédés Downstream (DSP) et passionné·e par l’optimisation des processus biopharmaceutiques ? Dans le cadre d’une mission  d’un an, rejoignez notre site de Corsier-sur-Vevey, au cœur d’un environnement technologique de pointe et collaboratif !Votre rôle :En tant que DSP Process Expert au sein de l’équipe MSAT (Manufacturing Sciences and Technology), vous jouez un rôle central dans le soutien aux opérations de production GMP. Vos

For our client, a company specialized in advanced technologies for the healthcare industry, we are looking for aCustomer Service SpecialistDuration: until end of Q1 2026Start date: as soon as possibleLocation: Greater Lausanne areaWorkload: 100% - 3 days/week remoteYour responsibilitiesHandle incoming customer and distributor inquiries via phone and email regarding orders, quotations, product requests, returns, or complaintsProcess sales orders and

Within the Global Drug Product Development function in our new center, we are looking for a highly motivated (senior) technician with practical experience in a chemical, biological or biotech laboratory. She or he will work together with other scientists within the team, as well as analytical scientists, throughout all steps of drug product development. Your role:Reporting to DP Development manager in the Early-Phase Drug Product Development unit, you

Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "DSP Manufacturing Senior Technician " who will support the DSP large-scale operations (GMP and pilot).You will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells. You will support the DSP activities from an operational and documentation point of view: column

Pour notre client basé dans le canton de Vaud, nous recherchons un(e) QA Manager – ISO 17025.  Rattaché(e) à la Direction, vous assurez la conformité réglementaire, la fiabilité des résultats analytiques et l’amélioration continue du système qualité du laboratoire. Vos responsabilités principales : Structurer, maintenir et faire évoluer le système documentaire qualitéVeiller à l’application des exigences ISO 17025 sur l’ensemble des processusPiloter les

The Technology & Innovation department strives to transform Global Drug Substance Development (GDSD) operations by exploring and evaluating cutting-edge technologies with agility and efficiency. Our mission is to create a diverse project portfolio that ranges from quick wins to visionary advancements and shine a light on future trends and empower our teams to embrace every challenge as an opportunity for growth.Key ResponsibilitiesThis position is

Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "DSP Manufacturing Associate Scientist " who will support the DSP large-scale operations (GMP and pilot).You will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells. You will support the DSP activities from an operational and documentation point of view:

We are looking for an Aseptic Operations Expert for a one-year mission to revamp one of our aseptic filling lines.As an Aseptic Operations Expert, you will ensure the highest standards of Sterility Assurance and Contamination Control during this one-year mission focused on the revamping of our filling line (Line 6) in the Fill & Finish (FDF) department. Your expertise will help ensure compliance with Annex 1 and other relevant GMP requirements,