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Pharma Technical Development (PTD) is a global team of over 2000 experts focused on developing innovative medicines to address patients needs.
Within PTD Synthetic Molecules Technical Development (PTDC) specializes in drug substance drug product and analytical sciences. PTDC is instrumental in advancing the synthetic molecules pipeline supporting research early development and clinical trials through technical innovation and collaboration.
This opportunity lies within analytical development for synthetic molecules where cutting-edge techniques like high-performance liquid chromatography gas chromatography ion chromatography and mass spectrometry are employed to develop efficient and robust analytical methods. The goal is to ensure the release of clinical trial products and their eventual commercial supply through a strong control strategy.
Take the lead in pioneering innovative analytical techniques while contributing to the successful delivery of clinical and commercial therapiesapply now and help shape the future of healthcare!
Development 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 (GMP) guidelines as well as the relevant SOPs.
Work on end to end processes in close collaboration with other associates 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 and validation reports.
Routinely apply GxP (GMP) requirements where necessary and understand how to exert them in different clinical phases.
You hold a solid vocational qualification with at least 1-3 years experience in the pharmaceutical industry with a strong focus on analytical methods development (i.e. chromatography) or a bachelors degree (Analytical Chemistry Biochemistry Biotechnology or related field). The role does not require any further academic qualifications.
Hands-on experience in analytical instrumentation and techniques (e.g. HPLC GC KF)
A strong interest / background in analytical methods development.
A good scientific writing style and good documentation practice for utilization of corresponding data in regulatory filings.
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.A strong quality mindset and excellent attention to detail.
Excellent command of English. Good command of German would be a plus.
Routinely apply GxP requirements where necessary and understand how to exert them in different clinical phases
We are looking forward to your application!
A healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver life-changing healthcare solutions that make a global impact.
Lets build a healthier future together.
Roche is an Equal Opportunity Employer.
Required Experience:
IC
F. Hoffmann-La Roche AG is a Swiss multinational healthcare company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange. The company headquarters are located in Basel.