Perform routine testing techniques such as the following, with a high degree of reliability, efficiency and accuracy:
HPLC/UPLC chromatography-based methods
Capillary electrophoresis based methods
Spectrophotometry based methods
Process related impurities testing based on ELISA, ddPCR
OD and TOC Test.
Compendials methods
Deliver data treatment and analytical reports of high quality.
Contribute to the writing of SOPs and analytics related documents in English.
Interact with customers when needed, with the aim of result discussion or coordination of routine activity.
In this role your responsibilities will include:
Perform routine testing techniques such as the following, with a high degree of reliability, efficiency and accuracy:
HPLC/UPLC chromatography-based methods
Capillary electrophoresis based methods
Spectrophotometry based methods
Process related impurities testing based on ELISA, ddPCR
OD and TOC Test.
Compendials methods
Deliver data treatment and analytical reports of high quality.
Contribute to the writing of SOPs and analytics related documents in English.
Interact with customers when needed, with the aim of result discussion or coordination of routine activity.
qualifications
Who you are:
You have a CFC or Bachelor's degree in biotechnology, chemistry, biochemistry or a related subject.
You have Knowledge of GLP/GMP/Quality Systems requirements for analytical testing
You have Knowledge in Empower, Softmax Pro, LIMS, Discoverant or other relevant software packages would be a plus.
You have good oral and written communication skills in English. French is a plus.
You have rigorous attention to details.
You have a high degree of self-motivation, commitment, reliability, flexibility, multi-tasking approach to support department and business objectives and a great team-spirit attitude.
You are curios and open minded to new tools & technology
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EK
Estelle Kotelon
Randstad Merck Aubonne
the application process.
See what comes ahead in the application process. Find out how we help you land that job.
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apply with randstad.
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we'll contact you.
Our consultant will call you at a suitable time to discuss your application and further career aspirations.
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getting you registered.
If you’ve never worked with us before, we’ll need some basic additional pieces of information to confirm your eligibility to work in Switzerland.
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compliance, reference and background check.
Next, we just need to verify a few things - we’ll make the relevant compliance checks and and in ensuring you’re perfect for the role, we’ll make contact with any relevant references you’ve provided and will keep you posted.
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the perfect job for you.
Our expert team will either arrange an interview for the role you’ve applied for, or if they believe there’s a better opportunity, they’ll suggest alternative options too.
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the interview.
We’ll ensure that you’re fully prepared ahead of your interview and know exactly what to expect - good luck!
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start your new job.
Congratulations, you’re ready to begin your new job. The team will ensure that you’re fully prepared for your first day.
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ongoing support.
After starting your new mission, we will contact you to check how you are doing and make sure you have our support in your new role.
En tant que membre de l'équipe QC Projet & Equipement, tu participeras aux activités de contrôle qualité liées à l'infrastructure du laboratoire et à la mise en ?uvre de nouvelles technologies.Ton rôle est de conduire notre évolution vers une automatisation accrue et un laboratoire de pointe par la validation de nouvelles méthodes analytique, la validation de feuilles excel et l'implémentation de nouveaux projets digitaux au sein du département. Tu support
En tant que membre de l'équipe QC Projet & Equipement, tu participeras aux activités de contrôle qualité liées à l'infrastructure du laboratoire et à la mise en ?uvre de nouvelles technologies.Ton rôle est de conduire notre évolution vers une automatisation accrue et un laboratoire de pointe par la validation de nouvelles méthodes analytique, la validation de feuilles excel et l'implémentation de nouveaux projets digitaux au sein du département. Tu support
As part of the QC Project & Equipment team , your will be able:To coordinate QC activities related to outsourcing Technology transfer and/or routine analytical activities .To ensure that all QC testing related to Tech Transfert are performed according to the established plan, good manufacturing practices, registration product files and site quality standards.To ensure that the documentation linked to the validation is done according to defined planning to
As part of the QC Project & Equipment team , your will be able:To coordinate QC activities related to outsourcing Technology transfer and/or routine analytical activities .To ensure that all QC testing related to Tech Transfert are performed according to the established plan, good manufacturing practices, registration product files and site quality standards.To ensure that the documentation linked to the validation is done according to defined planning to
TON RÔLE :En tant que membre de l'équipe QC Projet & Equipement, tu participeras à la mise en place de nouveaux équipements, en suivant les flux de qualification interne (IQ,OQ,PQ). Ces qualifications incluent une partie importante de CSV, pour garantir le respect de la data integrity.Ton rôle est de conduire notre évolution vers une automatisation accrue et un laboratoire de pointe par la qualification et la validation de nouveaux équipements et systèmes
TON RÔLE :En tant que membre de l'équipe QC Projet & Equipement, tu participeras à la mise en place de nouveaux équipements, en suivant les flux de qualification interne (IQ,OQ,PQ). Ces qualifications incluent une partie importante de CSV, pour garantir le respect de la data integrity.Ton rôle est de conduire notre évolution vers une automatisation accrue et un laboratoire de pointe par la qualification et la validation de nouveaux équipements et systèmes
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