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Technical R&D Senior Associate Scientist
vor 1 Monat
We make it GmbH ist ein national in der Schweiz agierendes Unternehmen, welches dank langjähriger und erfolgreicher Erfahrung über eine hohe Kompetenz im Personaldienstleistungsbereich verfügt. Konzentration der Vermittlertätigkeiten auf die Kernbereiche Industrie, Technik, Büro/Administration, Engineering, Pharma und Informatik. Die We make it GmbH stellt höchste Ansprüche an Qualität, Ethik und Diskretion.
Für unseren Kunden, die Firma F. Hoffmann La Roche mit Sitz in Basel, suchen wir eine/n
Technical R&D Senior Associate Scientist (m/w/d)
Background
In this role you are working in Analytical Development Synthetic Molecules within Pharma Technical Development. Analytical Development Synthetic Molecules is responsible for the development of resource and cost-efficient analytical methods using state of the art methodologies such as e.g. High-performance liquid chromatography (HPLC), Gas Chromatography (GC), Mass Spectrometry (MS), and others. The goal of our work is a robust control strategy to release products for clinical trials, and finally for commercial supply.
The perfect candidate: For this interesting challenge, you bring the following qualification: You have completed a vocational scientific qualification (e.g. apprenticeship) with at least 1 years’ experience in the pharmaceutical industry. An interest in analytical development for peptide analytics is a Plus. Applications of candidates with a Masters/bachelor’s degree (Analytical Chemistry, Biochemistry, Biotechnology or related field) who are willing to actively participate in lab work and routine measurements are considered as well.
AufgabenDevelopment, improvement and validation of analytical methods for the quality assessment of starting materials, intermediates, reaction monitoring, active substances and galenical forms
Thorough and efficient planning, execution and documentation of experiments in collaboration with the relevant team members, analytical project lead and your supervisor, following current GxP guidelines as well as relevant SOPs
Work on end-to-end processes in close collaboration with other associate scientists, scientists, and partners from other departments to ensure efficient analytics and continuous improvement
Coordination of analytical activities, including sample management for the development of synthetic products
Authoring of documents, e.g., analytical procedures, validation reports, user manuals, SOPs
QualifikationApprenticeship or a Bachelor /Master in analytical chemistry or in related field (*****)
1-3 years of work experience in lab environment preferable in a pharmaceutical industry (*****)
Hands-on experience in analytical instrumentation and techniques (e.g. HPLC, MS) (*****)
A good scientific writing style and good documentation practice for utilization of corresponding data in regulatory filings Excellent digital skills and an innovative mindset Preparedness to learn, continuously improve and apply novel ideas, tools and processes to quickly adapt to a fast-changing environment (*****)
Self-motivated, open-minded, proactive, reliable, goal-oriented and an excellent team player
You are open to new ways of working and support our team on the way to more flexibility and agility
(*****)
Excellent command of the English language. Good command of the German language would be a Plus
A stringent quality mindset and excellent attention to detail
Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phases
Nice to haves
Experience in analytical development for peptides is a Plus
Knowledge on LC-MS applications and instruments is a Plus
Experience in the field of large molecules/biologics analytics would be a Plus
Work hours
➢ Standard 40 h/ Week / Remote/Home Office: possible up to max. 10%
Sind Sie interessiert?
Dann freut sich Herr Andre Amstad auf Ihre vollständigen Bewerbungsunterlagen (Lebenslauf, Arbeitszeugnisse und Ausbildungsnachweise)