Technical Author - Basel

+We are looking for a Technical Author to join our team in Basel. You will work on high-level aeronautical projects within commercial, VIP, or defense aircraft programs. · +Support in building up the AMM and IPC supplements · Work independently on writing AMM supplements (all P/B ...

Develop high-quality maintenance and parts documentation for aircraft programs. · ...

Your primary responsibilities include supporting the development of AMM and IPC supplements by writing content according to airworthiness requirements. · Support in building up the AMM and IPC supplements · Work independently on writing AMM supplements (all P/B) according to airw ...

Wir suchen nach einer engagierten Technischen Author für unsere Abteilung Oligonucleotides. · ...

Bachem ist ein führendes, innovationsgetriebenes Unternehmen, das sich auf die Entwicklung und Herstellung von Peptiden und Oligonukleotiden spezialisiert hat. · Wir suchen eine/n engagierte/n Technische/n Author/in (w/m/d) zur Verstärkung unseres Teams in der Abteilung Oligonucl ...

At Novartis we are reimagining medicine to improve and extend people's lives Without safe easy-to-use high-quality drug delivery systems our patients could not get their medicines This is where you come in; the Device Technology Solution Center needs you as Senior Expert Engineer ...

We are seeking a Technical Regulatory Affairs CMC Associate Director to strengthen the team in 2026 in support of Phase 3 development activities. · ...

As a GMP Compliance Expert in the field of Enable Compliance you are responsible for the realization and Maintenance of the biotechnological chemical and galenic production facilities of the Pharmaceuticals Division at plants. · ...

+Job summary · This temporary hybrid videography position at Revnuu involves video production tasks such as camera operation lighting setup coordination execution of video shoots. · +ResponsibilitiesVideo production including pre-production planning post-production editing · Came ...

Congenius provides tailored expertise and leadership to global firms. If you enjoy working with a diverse range of people across a broad range of projects and are passionate about making a positive contribution to the MedTech industry. · Evaluate and develop new materials... · Co ...

The position of Senior Device Engineer at Roche involves leading cross-functional teams to develop combination products and medical devices. This includes evaluating new technologies, applying engineering knowledge to establish technical product requirements, and developing desig ...

The Principal Device Engineer will engage in extensive cross-functional collaboration with Quality Assurance (QA), Regulatory Affairs, Clinical, and Commercial teams to successfully bring combination products and medical devices to the market. · ...

Act as the technical authority for automation systems, including PCS7, Zenon and Isys platforms. · ...

The position of Deskside Technician – End User Computing performs troubleshooting, repair, · and preventative maintenance of end user computing equipment and peripheral equipment at corporate locations. · ...

We are reimagining medicine to improve and extend people's lives. We discover and develop breakthrough treatments and find new ways to bring cures to as many people as possible. Without safe, easy-to-use, high-quality drug delivery systems our patients could not get their medicin ...

The position is open for a Quality Specialist to support our Basel based client in the Pharma sector. · ...

As an SAP ABAP OO Developer, you will be part of a dedicated team driving innovation within our SAP system landscape. · ...

We are seeking an Associate Director Science & Technology for drug product formulation and process development of parenteral innovative medicines. · Authors source documents for regulatory submissions. · Lead and manage project and network cross-functional team activities. · ...

+Regulatory affairs associate for a leading global pharmaceutical company based in Basel's BioValley region. · ...

Quality Specialist responsible for standard activities and supportive project work. Supports the timely release of GMP relevant documents and batches. · ...