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 Europes 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.
The Technical Project Leader Drug Product will lead the technical development (all kind of formulations, mainly oraldosage forms) and CMC team (Chemistry Manufacturing and Control) of several projects from early phase development activities up to commercialization, including production scale up with external partners.
Lead the development, communication and execution of the overall CMC strategy.
Lead and managedevelopment, analysis and productionofdosage forms, including clinical and market forms. Ensure sufficient and timelysupplies for development projects based on input from the Planning & Procurement, CMC, Project and/or Life Cycle management functions
Leading the collaboration with external development partnerswith special emphasis on cost efficiency, timelines and scientific quality
Lead the technical drug productdevelopment 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 7years job relevant working experience in the pharmaceutical industry
Scientific expertise in oral and parenteral formulations
Proven know how of development of dosage forms to be used in combination products.
Profound knowledge of GMP, quality control and pharmaceutical development and/or production processes, based on current guidelines
Profound knowledge in QbD, DOE and QRM
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
A competitive salary and generous social benefits
Business Area:Pharmaceutical Development
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.