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.
Technical Project Leader Drug Product (parenteral combination product)
The Technical Project leader Drug Product will mainly lead the technical development of a parenteral combination product from early phase activities up to commercialization and production scale up with external partners. The candidate will eventually also be responsible for other projects with all kind of formulations (e.g. oral solid dosage form).
Lead and manage development, analysis and production of dosage forms, including clinical and market forms
Ensure sufficient and timely supplies for development projects based on input from the Planning & Procurement, CMC, Project and/or Life Cycle management functions
Leading the collaboration with external development partners with special emphasis on cost efficiency, timelines and scientific quality
Lead the technical drug product development activities: plan, organize and administer the different aspects of the technical activities required for development, scale-up, validation and manufacturing of a drug from early development up to commercial supplies
Ensure compliance with regulatory guidelines
Pharmacist or Equivalent with PhD
Minimum of 5 years job relevant working experience in the pharmaceutical industry
Scientific expertise in parenteral (lyophilization) formulation and preferably device development
Profound knowledge of GMP, quality control and pharmaceutical development and/or production processes, based on current guidelines
Knowledge in QbD and DOE
Ability to negotiate, plan, and coordinate technical development and manufacturing activities
Excellent interpersonal skills with the ability to adapt effectively to rapidly changing organization issues, structures and dynamics
Excellent English knowledge (oral and written)
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
If you are interested, please send your CV and motivation letter by email to firstname.lastname@example.org clearly stating the job title and reference of the position to which you are applying in the subject line.
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.