Technical R&D Senior Associate Scientist (m/f/d)
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Technical R&D Senior Associate Scientist (m/f/d) for F. Hoffmann La Roche
We make it GmbH is a company operating nationally in Switzerland which, thanks to many years of successful experience, has a high level of expertise in the personnel services sector.
Its recruitment activities are focussed on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make it GmbH places the highest demands on quality, ethics and discretion.
For our client, F. Hoffmann La Roche, based in Basel, we are looking for a
Technical R&D Senior Associate Scientist (m/f/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), Ion Chromatography (IC), Mass Spectrometry (MS), and others. The ultimate 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 either have a Masters/Bachelors degree (Analytical Chemistry, Biochemistry, Biotechnology or related field) OR you have completed a vocational scientific qualification (e.g. apprenticeship) with at least 3-5 years experience in the pharmaceutical industry with a strong focus on analytical development for peptide analytics.
General information
Start date: asap
latest Start Date: 1.10.2024
Planned duration: unlimited
Workplace: Basel
barrier free Workplace: no
Workload: 100%
Remote/Home Office: max. 10% remote
Travel: no
Team: 10
Used Template: CH_Senior Laboratory Worker_LSB_CHF_RCM
Department: Development APL Team 1 (MMDCAA)
Working hours: Standard
Is a criminal record extract required: no Working hours: Standard
Task and Responsibilites
- Development, improvement and validation of analytical methods for the quality assessment of starting
materials, intermediates, reaction monitoring, active substances and galenical formsThorough 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
Qualifications
- Hands-on experience in analytical instrumentation and techniques (e.g. HPLC, MS) (*****)
- Strong knowledge on LC-MS applications and instruments is a plus
- A strong interest/background in analytical development for peptides (****)
- Experience in the field of large molecules/biologics analytics would be a plus
- 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
Work hours
Standard 40 h/ Week
Are you interested?
Then Mr. Andre Amstad looks forward to receiving your complete application documents (CV, work reference letters and training certificates).
We look forward to hearing from you
