Be at the forefront of cardiometabolic innovation in Switzerland. Shape how leading clinicians understand and apply breakthrough treatments that transform patient lives! Your new role As Medical Science Liaison Manager East, youll establish Novo Nordisk as
About Us ten23 health is a human-centric and sustainable strategic partner of choice for the pharmaceutical industry and biotech start-ups for the development, manufacture, and testing of tomorrow’s medicines. We support our clients in developing differentiated,
Quality Manager for Compliance & GDP Processes (m/f/d) YOUR TASKS AND RESPONSIBILITIES: This position offers an exciting opportunity for you as a senior quality professional to oversee and advance the Quality Management System (QMS) for BCC
Overview: The Manager, Clinical Trial Authorization (CTA) is responsible for ensuring that CTA activities for assigned clinical studies are planned, governed, and overseen in line with CSL regulatory expectations, quality standards, and development timelines. Reporting to
Overview This position supports the entire QC team in continuous improvement activities at the STA Pharmaceutical Switzerland SA site. The Specialist QC Operational Excellence plays a pivotal role in ensuring that products and processes meet stringent
Since over 170 years Pfizer colleagues from all over the world are working together to positively impact health for everyone, everywhere. Apart from marketing over 100 products in the Swiss market, the Pfizer AG commits itself
MISSION Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with
The eTMF Specialist, Regulatory Affairs is responsible for the maintenance, quality, and inspection readiness of the electronic Trial Master File (eTMF) documents owned by Regulatory Affairs. The role ensures eTMF-relevant regulatory documentation is complete, accurate, timely,
Analytical Compliance Record Specialist Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in Personalised Healthcare. As the world’s largest R&D spender in the pharmaceutical and diagnostics domain, they work
GRANITE BIO is a private biotechnology company located in Basel (Switzerland). GRANITE BIO is supported by top-tier investors with ~$100M raised to date. Based on fundamental research conducted over the last two decades, GRANITE BIO’s is
Obstetrician/Gynaecologist Jusluis, an MSF obstetrician-gynaecologist, provides a family planning consultation. Venezuela, March 2022. © Jesus Vargas Jobs in the Field Obstetrician/Gynaecologist Jusluis, an MSF obstetrician-gynaecologist, provides a family planning consultation. Venezuela, March 2022. © Jesus Vargas
Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together,
Manager and Senior Manager in Life Sciences R&D Management Consulting Grow here. Go further. Zürich Per Agreement 100% Advisory Everyone welcome ID: WD Your Impact As a Manager / Senior Manager in our fast growing Life
Position Summary For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market positioning. Specifically, evidence must be generated and maintained throughout the product lifecycle as the
Main Responsibilities: Maintain Regulatory Affairs content within the eTMF in accordance with regulatory requirements, ICH guidelines, and internal SOPs. Liaise closely with third parties to obtain regulatory eTMF documents. Prepare and perform ongoing quality control (QC)
A leading biopharmaceutical company in Switzerland is seeking a Responsible person to oversee Quality Compliance for pharmaceutical products. The ideal candidate should possess a degree in Chemistry, Pharmacy, Biology, or a related field, with a minimum of
Aperçu With a reporting line in the Quality Assurance team, this position leads the daily Quality System activities and related operations associated with the development and the maintenance of a Quality Management System for Incyte manufacturing