R&d Scientist

Vor 2 Tagen

Bern, Schweiz Consultys Switzerland Vollzeit

**About Us**

Consultys Group is a 100% specialist LifeScience consulting firm. With more than 550 experts working in France, Belgium, Germany and Switzerland on major engineering, R&D and compliance projects for the world's leading pharmaceutical, medical device and biotech companies.

Consultys links operational compliance, quality, processes, R&D, regulatory, own solutions and technology in ways that master complex business challenges to help its LifeScience clients exploit their existing strengths and develop new capabilities by combining its experience and innovative thinking across in the regulated environment.

**Role & Responsibilities**
- Execute analytical development activities for new drug product development, including pre-formulation studies, method development, method validation, and stability studies utilizing analytical instrumentation such as HPLC, UPLC, GC, FT-IR, UV-Vis, dissolution apparatus, and wet chemistry, as applicable
- Responsible for the independent execution of analytical project deliverables, as well as the authoring of technical documents such as analytical method
- Validation protocols and reports in compliance with standard operating procedures and regulatory requirements.
- Design new drug therapies using natural or synthetic (man-made) ingredients
- Determine the most effective formulation and dosage for a specific drug
- Work on improving the drug manufacturing process
- Document all the developments in experiments and researches
- Conduct experiments and analyzing results
- Collaborate with different researchers, academics, scientists and research institutes to aid in the development of drug
- Use computer technology for research and development
- Set up and follow safety measures in the place of work

**Requirements**:

- Hands-on personality, with flexibility and dedication to maximize our client's value
- Masters' degree and/or PhD in Analytical Chemistry, Biotechnology, Biochemistry or related field
- At least 2 years of experience in GMP pharma business activities
- More than 1 year of experience in GMP laboratory activities, for the research and development of new API and drugs
- Cell culture experience is plus
- Hands-on experience on instrumentation, data acquisition and analysis is preferred
- Ability to effectively work as part of a multidisciplinary, international team
- Hands-on personality, with flexibility and dedication to maximize our client's value
- Fluency in English is required, German, French or Italian would be a plus

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