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- ...Our client is seeking an experienced Senior Documentation Quality Specialist to act as a subject matter expert for the quality of clinical, nonclinical, and regulatory documentation. The role ensures that key deliverables are clear, accurate, consistent, compliant, and...QualitätTemporärVollzeit
- Hast du ein abgeschlossenes naturwissenschaftlich-technisches Studium (z. B. Pharma oder Chemie) sowie 1 bis 3 Jahre Berufserfahrung in der pharmazeutischen Qualitätskontrolle oder Produktion unter GMP-Bedingungen? Wir freuen uns, von dir zu hören! Allgemeine Informationen...QualitätSelbständige TätigkeitSoforteinstellungHomeoffice
CHF 133700 pro Jahr
...to offer relocation support for this role. Please only apply if this location is accessible for you. Are you ready to shape the quality strategy behind some of the world's most innovative medicines? As Global Head CQA Development Unit, you will play a pivotal...QualitätFlexible Arbeitszeit- ...begleiten wir in ihrer beruflichen Entwicklung und finden für sie zu ihrer jeweiligen Lebenssituation passende Karrieremöglichkeiten. Quality Systems Specialist ITOT Unser Kunde ist ein Pionier in der Arzneimittelforschung und -entwicklung und einer der Vorreiter in der...QualitätSelbständige Tätigkeit
- ...is to discover, develop, and commercialize innovative medicines to help more patients. Stellenbeschreibung Provide GMP/GDP quality assurance expertise during development and commercialization of clients products Ensure all required quality activities are initiated...QualitätVollzeit
CHF 82600 - CHF 153400 pro Jahr
...international partners to advance innovation programs. Lead process improvement initiatives that enhance operational efficiency and service quality. Mentor and train colleagues on patent prosecution processes and intellectual property administration. Support cross-...QualitätFlexible Arbeitszeit- ...The Trial Data Manager leads end-to-end Data Management activities for assigned clinical trials, ensuring high-quality, consistent data delivery in line with internal standards, applicable regulations, and agreed timelines. The role coordinates eCRF development, data...QualitätTemporärVollzeit
- Summary We are looking for a dedicated QC Analyst to support Good 'x' Practice (GxP) activities in our quality department. This role involves managing quality systems, implementing operational processes and ensuring compliance with Novartis quality standards...QualitätSchichtarbeit
CHF 160 - CHF 270 pro Tag
...passionate about delivering excellent customer service. We are looking for a dependable individual who takes pride in producing high-quality work and contributing to a positive, professional workplace. The ideal candidate is organized, reliable, and able to manage...Qualität- ...manufacturing. Communicate and coordinate with suppliers and manufacturers regarding part and assembly production, sourcing and quality issues. Create documentation to be submitted for FDA (US) or Notified Body (EU) approval for medical devices. Ensure the maintenance...QualitätVollzeit
CHF 65870 - CHF 122330 pro Jahr
...Supporting both low molecular weight and radioligand therapy projects, you will collaborate across disciplines and sites to generate high-quality scientific insights that advance oncology drug discovery. About the Role Key Responsibilities Develop and execute...QualitätPostdoc StelleFlexible Arbeitszeit- ...fairness and consistency, including employee relations, employee communication, training and development, coaching and counselling, quality of life and leadership training. The Human Resource Manager reports to Captain. WHAT YOU WILL DO ON BOARD Provide...Qualität
- ...multiple systems and channels. Collaborate closely with infrastructure, release management, and development teams to ensure high-quality solutions from design through deployment. Support testing activities, production rollouts, and ongoing service improvements....Qualität
- ...reproducible data-analysis workflows; Experience working with complex, high-dimensional biomedical or imaging datasets, including data quality control and validation; Ability to explain technical methods and results clearly to both computational and clinical...Qualität
- ...multiple systems and channels Collaborate with infrastructure, development and release management teams Ensure end-to-end solution quality from design through deployment Support testing activities, releases and production rollouts Your Profile: ~ Degree in...QualitätFestanstellung
- ...Director of Technology & Engineering within Novartis Biomedical Research Data & Digital Software & Workflows, you will shape how high-quality, AI-enabled software solutions are designed, built, and delivered across scientific workflows and laboratory processes. You will...Qualität
- ...clear investment insights Work closely with Portfolio Management, Investment Compliance and Operations to maintain robust data quality and ensure reporting is delivered accurately and on time Support the continued enhancement of risk and performance analytics, including...QualitätFestanstellung
- ...world evidence studies, and other HEOR analyses. Managing external HEOR and evidence-generation vendors, ensuring delivery of high-quality outputs aligned with JCA timelines and business needs. Reviewing study protocols, analysis plans, reports, and evidence...QualitätTemporärRemote job
- ...Target Assessment through Lead Optimization across different disease areas. You will integrate deep scientific expertise with high quality execution of discovery programs. The Opportunity Therapeutic Design Strategy: Lead the drug design strategy of oligonucleotides...Qualität
- ...and with the PI, postdocs, and PhD students who analyze the data. Your work ensures that every dataset entering the lab is secure, quality-controlled, and analysis-ready, and that the computational environment is reliable and reproducible. In line with our and Uni Basel...QualitätPostdoc StelleSoforteinstellungFestanstellung
- ...No Stellenbeschreibung Development and optimization of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, KF) for the quality assessment of starting materials, intermediates, and active pharmaceutical ingredients (APIs). Planning and meticulous execution...QualitätTemporärVollzeitHomeoffice
CHF 146300 pro Jahr
...including M&A, research collaborations, and in-licensing opportunities, with advice on contract drafting and negotiation Ensure high-quality, timely delivery of work aligned with business goals and budgets Essential Requirements University degree in law, admission...QualitätFlexible Arbeitszeit- ...innovative statistical methodolog ies to support drug development; and overseeing external vendors and CRO to ensure high quality , timely and compliant deliverables . Essential Functions: ~ Serves as the lead statistician and primary statistical...Qualität
- ...forms that support cutting-edge clinical trials. Joining our TRD PHAD Oral Supply team, you will work in a highly collaborative and quality-focused environment where your expertise directly contributes to the development of new treatments and helps transform patients’...QualitätFlexible Arbeitszeit
- ...strategy implementation in collaboration with other colleagues within Safety Science, chairs benefit–risk discussions and ensures high‑quality safety deliverables within cross‑functional product teams, including active participation in the Medical Development Team (MDT),...QualitätVollzeit
- ...Revolution Medicines seeks an experienced Principal Regulatory Medical Writer in Basel to author and coordinate high-quality regulatory documentation for European clinical development and marketing authorization activities. The role involves leading complex submissions...Qualität
- ...reports to the Senior Director, EU Legal Counsel. This position will support all international functions (Commercial, Supply Chain, Quality, Clinical, Medical Affairs, Compliance…) in day by day activities. Responsibilities will span a wide range of duties ensuring that...QualitätRemote job
- ....) Be the local contact for customers Be the guarantor of quality and HSE policy Report to the office director concerning the... ...chemical, pharmaceutical or other process industries. Personal qualities: Strong management potential / Industrial culture / Ability to...QualitätVollzeit
- ...pharmacovigilance portions of regulatory filings and clinical documents Develop controlled documentation for pharmacovigilance oversight and quality system demonstration Collaborate with EU Qualified Person for Pharmacovigilance on European regulatory compliance...Qualität
- ...Responsibilities Develop and execute EU labelling strategy aligned with global regulatory approach Prepare and oversee high-quality labelling documents for EU, UK, and Swiss submissions Serve as regional labelling subject matter expert, advising internal teams...Qualität
