Healthcare Product Manager

Job DescriptionYou will participate in Product Life Cycle Management activities, helping us shape the future. You will prepare and support market launches and launch tracking, conduct market research and competitor analyses, and apply theoretical knowledge in practice.You will analyze sales and financial data with SAP and learn to use the corresponding tools...

Job DescriptionAs a Sr. Manager, Corporate Affairs, you will be responsible for developing and implementing an integrated communications strategy that encompasses internal and external communications, issues management, brand/corporate communications, and reputation management for Rare Disease, FA, SMA, and ALS.You will work closely with cross-functional...

About the RoleWe are looking for a highly motivated and experienced Sr. Manager, Corporate Affairs to join our International Corporate Affairs team in Baar, Switzerland.The ideal candidate will have a strong background in corporate and/or marketing communications, with at least 5 years of experience in the healthcare industry.The role will involve developing...

About the Role:This is an exciting opportunity for a seasoned Regulatory Affairs professional to join our team in Switzerland. As a Regulatory Affairs Manager, you will play a key role in ensuring compliance with medical device regulations, supporting product development, and collaborating with cross-functional teams.

Sr. Manager, Corporate AffairsThe role of Sr. Manager, Corporate Affairs is to develop and implement an integrated rare disease communications strategy that encompasses internal and external communications, issues management, brand/corporate communications, and reputation management for Rare Disease, FA, SMA, and ALS.This includes developing and...

We are seeking a highly experienced Manager, International Communications to join our team in Switzerland. As a key member of our International Corporate Affairs team, you will play a critical role in supporting our Rare Disease Lead in developing and implementing an integrated communications strategy that drives business results.Your primary responsibility...

We are seeking an experienced Integrated Quality Manager to join our team at TN Switzerland. As a QA Associate III, you will play a vital role in ensuring product safety, efficacy, and purity through comprehensive quality assurance practices.The ideal candidate will have a Bachelor's or Master's degree in Chemical Engineering, Bioengineering, Biotechnology,...

Job Description:About the RoleWe are seeking a highly experienced Senior Manager, Global Communications Strategy to join our team in Switzerland. As a key member of our International Corporate Affairs team, you will play a critical role in supporting our Rare Disease Lead in developing and implementing an integrated communications strategy that drives...

About the Team:Our team is passionate about ensuring the safe use of pharmaceutical products. As a Senior PV Scientist, you will have the opportunity to work alongside talented professionals who share your commitment to excellence.About the Role:Leverage your pharmacovigilance expertise to drive business growth and success.Develop and implement innovative...

Join our team as a Head of Rare Disease Communications and take on a challenging role that requires strategic thinking, exceptional communication skills, and a passion for the rare disease space. As a key member of our International Corporate Affairs team, you will play a critical role in developing and implementing an integrated communications strategy that...

Your main tasks Focus of this position is supporting our rapidly developing Diabetes Care (active and connected devices) Manage the development and implementation of regulatory strategies Support and prepare product submission documents with main focus on EU and US Partner with business stakeholders on different levels Communication and...

Job Overview:We are seeking a highly skilled Regulatory Affairs Manager to support our rapidly developing Diabetes Care portfolio. This role will be responsible for managing the development and implementation of regulatory strategies, preparing product submission documents for EU and US markets, and partnering with business stakeholders.

Your main tasks Build test automation solutions, encompassing the necessary documentation framework and evidence definitions Strong technical knowledge in develop, enhance, and introduce verification methods, processes, and tools. Programming languages knowledge - JAVA , PYTHON Define test strategies for the subsystem/system under verification ...

Your main tasks Perform medical assessments of technologies and therapies for the treatment of diabetes and translate into comprehensible insights to drive strategic decisions Develop, maintain and deliver medical and educational training programs to support the adoption of Ypsomed's solutions Create scientific materials to support the...

This is a part-time job that offers the opportunity to work in a dynamic and growing organization. We are seeking a highly experienced Director, Corporate Affairs and Reputation Management to join our team in Switzerland.As a key member of our International Corporate Affairs team, you will play a critical role in supporting our Rare Disease Lead in...

As a Senior PV Scientist at TN Switzerland, you will play a critical role in ensuring the safe use of medicinal products.This role will involve collaborating with Global Safety Officers and other Safety MDs for assigned investigational programs.Education and Experience Requirements:Bachelor's Degree or MSc in biologic or natural science; or health care...

Kraftort. Ypsomade. Im Bereich Quality Management, Regulatory & Medical Affairs in der Abteilung Quality Assurance suchen wir am Standort Solothurn eine kundenorientierte und qualitätsbewusste Persönlichkeit als Quality Assurance Manager | - % Ref-Nr. 7 Arbeitsort: Solothurn , Burgdorf | Hybrid Helfen Sie uns, modernste Medizintechnik-Lösungen auf...

We are seeking a highly skilled QA Associate to join our Integrated Downstream Quality Operations team.In this role, you will engage in quality operations and engineering activities for downstream manufacturing and equipment at a large-scale facility. Your focus will be on ensuring product safety, efficacy, and purity through comprehensive quality assurance...

**Job Responsibilities:**As a Quality Control Specialist for Downstream Operations, you will be responsible for ensuring the quality and safety of pharmaceutical products throughout the manufacturing process. This includes:Reviewing and approving GMP documents, such as procedures, work instructions, CAPAs, deviations, change control, equipment qualification...

**Job Description:**We are seeking a highly skilled Pharmaceutical Quality Assurance Expert to join our team at Michael Page International (Switzerland) SA. As a GMP Specialist, you will be responsible for ensuring the quality and safety of pharmaceutical products throughout the manufacturing process.In this role, you will:Review and approve GMP documents,...