Job Detail

Senior Lab Technician AD/QC (1 year temporary)

Inseriert am: 14.06.2018

Senior Lab Technician AD/QC (1 year temporary)

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.


 


Job 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 Temporary Lab Technician working in AD/QC will have the following responsibilities and tasks:



  • Development, optimization and application of analytical methods, e.g., for purity-, stability-, content determinations, identity tests

  • Write-up of analytical methods for implementation (GMP and non-GMP)

  • Conduct of validation, release, retest, and transfer analyses (all GMP)

  • Proper documentation/presentation of analytical data (non-GMP developmental activities and GMP-activities according to Good Documentation Practices through compilation of all analytical testing records (e.g., notebooks, raw data hardcopies))

  • Conduct of stability studies (GMP and non-GMP)

  • Interpretation and documentation of analytical data including results from method development, release, retest, validation, stability, and transfer

  • Write-up of analytical protocols and reports, e.g., for validation and stability studies

  • Handling of laboratory equipment according to respective SOPs

  • Assurance of adequate maintenance and operation of analytical equipment according to GMP

  • Drafting and review of CoAs

  • Drafting of SOPs

  • Training of Laboratory Technicians on routine tasks

  • Ensuring of cleanliness of laboratory and work space


 


Candidate Requirements



  • Apprenticeship-, college-, or university-degree or equivalent education in the field of chemistry, biochemistry, pharmacy, or chemical engineering with a minimum of 2 years’ experience.

  • Ability to efficiently plan and effectively execute and document analytical experiments in a GMP-compliant pharmaceutical environment.

  • Good knowledge of GMP and sample preparation, HPLC instrumentation and techniques.

  • Basic knowledge of spectroscopic methods, e.g. UV/VIS, IR, NMR, MS.

  • Good trouble-shooting skills for analytical analyses.

  • Flexibility, good communication, time management and team-working skills.

  • Ability to work independently and to take initiative

  • Good command of English (written and spoken)


 


What Idorsia offers



  • 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
Country: Switzerland
Business Area: Pharmaceutical Development
Schedule: Fulltime
Job Type: Temporary for 1 year
Job ID: 926


 


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.

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