Temporary Assistant Scientific Associate
vor 19 Stunden
**About Idorsia Pharmaceuticals Ltd**
Idorsia Ltd is reaching out for more - We have more ideas, we see more opportunities and we want to help more patients.
In order to achieve this, we want to develop Idorsia into one of Europe’s leading biopharmaceutical companies, with a strong scientific core.
Headquartered in Switzerland - a European biotech hub - Idorsia is specialized in the discovery and development of small molecules, to transform the horizon of therapeutic options. Idorsia has a broad portfolio of innovative drugs in the pipeline, an experienced team, a fully-functional research center, and a strong balance sheet - the ideal constellation to bringing R&D efforts to business success.
Idorsia was listed on the SIX Swiss Exchange (ticker symbol: IDIA) in June 2017 and has over 1,000 highly qualified specialists dedicated to realizing our ambitious targets.
We are looking for a motivated **Temporary Assistant Scientific Associate** to join our dynamic team
**Responsibilities**:
- Analytical Development / Quality Control (AD/QC) is dealing with the analytical development of Drug Substance (DS) and Drug Product (DP)._
- AD/QC must ensure that products are delivered according to quality standards defined during development and in compliance with GMP and regulatory guidelines._
The Assistant Scientific Associate working in AD/QC will have the following responsibilities and tasks which are related to the company site Idorsia Pharmaceuticals Ltd, Allschwil, Switzerland:
- Active participation in Sampling activities for excipients and packaging material in collaboration with Clinical Manufacturing units of Idorsia Pharmaceuticals.
- Internal laboratory activities execution for excipients and packaging material when needed. Follow the processes defined in Guidelines and SOP’s.
- Drafting of certificate of analysis for excipients and packaging material according to USP and Ph. Eur.
- Active participation of visual inspection activities and related documentation internally and with external partner following GMP regulations.
- Collaboration with clinical manufacturing unit 1 for swabbing activities in the frame of cleaning verification.
The assistant scientific associate of the MOS group may fulfill the following activities:
- Conduct of release, retest, stability studies, transfer and validation analyses.
- Proper documentation of all analytical activities according to Good Documentation Practices through compilation of all analytical testing records (e.g., notebooks, raw data hardcopies).
- Interpretation of analytical data
- Ensuring of cleanliness of laboratory and work space.
- Handling of laboratory equipment according to respective SOPs.
- Apprenticeship-, college-, or university-degree or equivalent education in the field of chemistry, biochemistry, biology, pharmacy, or chemical engineering
- Ability to efficiently plan, execute and document analytical experiments in a GMP-compliant pharmaceutical environment
- Basic knowledge of sample preparation, HPLC techniques and instrumentation
- Good communication and team-working skills
- Proficient in English
**What Idorsia offers**
- Exciting opportunities for development and professional growth within our dynamic organization
- A collaborative and solution-oriented environment where you can make a difference
- An innovative and open culture in a truly multicultural environment
- A competitive salary and generous social benefits
**Work Location**: Allschwil (Basel Area)
**Country**: Switzerland
**Business Area**: Global Pharmaceutical Development & QA - Analytical Development and Quality Control Drug Products
**Schedule**: Fulltime
**Job Type**: **Temporary for 1 year**
**Job ID**: 3293
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