Zur Verstärkung des bestehenden Teams in unserer Wirkstoffproduktion suchen wir zum nächstmöglichen Zeitpunkt eine/n engagierte/n Technical Author Peptide Manufacturing (a), 100% (temporär für 12 Monate mit Aussicht auf Übernahme). Sie sind verantwortlich für das Schreiben produktionsrelevanter GMP-Dokumente
Zur Verstärkung des bestehenden Teams in unserer Wirkstoffproduktion suchen wir zum nächstmöglichen Zeitpunkt eine/n engagierte/n Technical Author Peptide Manufacturing (w/m/d), 100%. Sie sind verantwortlich für das Schreiben produktionsrelevanter GMP-Dokumente und sind in dieser Rolle auf eine Produktionseinheit
The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Join our Manufacturing Operations team in Visp, where you will play a key role
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description Are you ready to make a meaningful impact in the world of science? Join Thermo Fisher Scientific as a Senior
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
Entyre Group is one of the fastest-growing health tech scale-ups in Europe and the United States. We are based in Zurich, Berlin, and Boston, Chicago, Detroit, Washington D.C., and other locations and employ over 500 people,
When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This role offers the opportunity to lead and shape a comprehensive contamination control
he actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Today, Lonza is a global leader in life sciences operating across five continents.
QA Engineer – Mobile Testing We are looking for a QA Engineer with a strong focus on mobile testing to join our team. The SBC App Team within the Specialized Global Tech unit is responsible for
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Job Description The Global Clinical Supply (GCS) organization manages the “end-to-end” clinical supply for the company’s portfolio. GCS is accountable for the planning, sourcing, labelling, packaging and delivery of clinical supplies to clinical sites across more
To drive our continuous organic growth, we are constantly looking for highly qualified professionals. To strengthen our team in the Global Engineering department, we are looking for a dedicated Senior Commissioning & Qualification (C&Q) Lead (f/m/d),
To drive our continuous organic growth, we are constantly looking for highly qualified professionals. To strengthen our team in the Global Engineering department, we are looking for a dedicated Senior Commissioning & Qualification (C&Q) Lead (f/m/d),
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
At Sunrise, we think bigger, go further and create new ideas. For us working culture means achieving great things together. It’s where respect and innovative ideas combine with real teamwork – every voice counts, every perspective
Principal Scientist, Pathogen Safety Support The Opportunity The Principal Scientist, Pathogen Safety Support provides scientific and operational expertise to support pathogen safety activities across manufacturing, technical operations, and product lifecycle management. This role partners closely with
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
Um unser kontinuierliches Wachstum voranzutreiben, suchen wir laufend hochqualifizierte Fachkräfte. Zur Verstärkung unseres Teams im Bereich TechOps suchen wir eine engagierte Persönlichkeit als Head Technical Documentation Sisslerfeld (w/m/d) 100% Im Rahmen des Aufbaus unserer neuen Greenfield-GMP-regulierten
Overview The Manager, GMP Quality is responsible for the oversight and day-to-day quality interface with CDMO producing DS & DP for MRTxs ongoing clinical programs. This includes supporting the review of MBRs/EBRs, analytical methods, validation protocols/reports,