Trainee in Quality Assurance GLP

Location: 

Basel Area - Allschwil, BL, CH

 

 

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 will develop Idorsia into one of Europe’s leading biopharmaceutical company, 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 600 highly qualified specialists dedicated to realizing our ambitious targets.

 

We are looking for an enthusiastic and motivated Trainee in Quality Assurance GLP to join our team.

 

The trainee will undertake a range of tasks to verify that non-clinical safety studies and analytical laboratory activities are planned, performed, conducted, reported and archived in accordance with international GLP regulations. 

 

Responsibilities :

 

  • Audit laboratory data and records to assure compliance with the study plan, GLP principles, Standard Operating Procedures and verify data integrity
  • Review study plans to verify compliance with GLP regulations
  • Audit draft study reports against the raw data and supporting study documentation to confirm that the report is a true reflection of the raw data, is internally consistent and that GLP requirements have been met
  • Assist in the planning, performance and reporting of QA audits
  • Ensure timely logging of QA activities, audit observations and retention of QA records
  • Participate in the preparation and management of Standard Operating Procedures and associated training documentation
  • Undertake record management activities and archive documents in accordance company policy

 

Requirements :

 

  • Apprenticeship, college-, or university-degree or equivalent education in the field of chemistry, biochemistry, biology, pharmacy, or chemical engineering
  • Previous experience working in Quality Assurance, a Good Laboratory Practice (GLP) environment or an analytical laboratory would be advantageous
  • Strong interpersonal skills and the ability to develop good working relationships with internal and external colleagues
  • A systematic approach with a good eye for detail
  • Excellent communication and organisational skills
  • Ability to work independently or as a team
  • Good command of written and spoken English

 

What Idorsia offers

 

  • Exciting opportunities  for development and professional growth within our dynamic organization
  • A collaborative and solution oriented enviroment where you can make a difference
  • An innovative and open culture in a truly multicultural environment

 

 

Work  Location: Allschwil

Country: Switzerland

Business Area: Quality Assurance

Schedule: Fulltime

Job Type: Temporary ( until end of January 2021)

Job ID: 1439

 

If you are interested, please click on apply now.

Please be informed that if you are selected for this position, your employment will be subject to a pre-employment background screening process, of which you would be informed in greater detail in due course.

Please note Idorsia operates a strictly-controlled list of preferred recruitment partners. For those partners who have no valid, signed Master Service Agreement in place with Idorsia all unsolicited resumes, CVs, anonymous profiles, or any other candidate details submitted through our website or to personal e-mail accounts of employees of Idorsia Pharmaceuticals (including any of its subsidiaries, affiliates or related companies) are considered the property of Idorsia Pharmaceuticals and are not subject to payment of any form of introduction, placement or referral fees.