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• Plan and perform drug discovery contract research studies using liquid handling platforms
• Study related client communication in English
• Data evaluation and interpretation
• Summarize data, analyze results and formulate conclusions
• Work with other project team members and communicate results with the team

• Innovatív oltóanyagok tervezése, fejlesztése és előállítása laborméretben a CEVA új generációs vakcinaportfóliója részeként együttműködésben belső és külső partnereinkkel
• Tech transzfer & méretnövelés támogatása folyamatoptimalizálás révén

CSV Engineer You can find all of our job offers by clicking here: /. Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. Teoxane strength is to offer a global patient...

QA Specialist (f/m/d) - CSV & QV In Bern, we're not just expanding-we're reaching a major milestone by launching a new production site and introducing innovative ways of working. This is what being a Persistent Pioneer in our BN DNA is all about-bringing a pioneering spirit to everything we do....

Provide deep medical expertise across relevant therapeutic areas, ensuring continuous awareness of scientific and clinical developments and effectively disseminating updates to Medical Affairs and, where appropriate, to commercial teams. Lead, coach, and develop a team of Medical Affairs Managers...

• Planning, designing, and performing (primary) cell–based, molecular biological, and biochemical experiments
• Conducting animal experiments using mouse models
• Establishing new project-related laboratory methods, including experimental design, implementation, and validation of results

• Cover the PRRC role when requested from the needs of the company (e.g. during the absence of the current PRRC)
• Develop and execute regulatory strategies for products and services
• Provide regulatory expertise for complex or unique issues and challenges regarding registration and compliance activities.

• Management of the QC department, including responsibility for budget and personnel
• Ensuring the timely QC testing of relevant materials (e.g., raw materials, intermediates, drug substances, finished drug products)
• Responsibility for method qualification/validation

• Build, lead, and develop an international team to achieve sales and market development goals
• Own regional responsibility for ECMO business development in EMEA, Eastern Europe, and Latin America, including assigned product partners

• Line manager for the organization/project management of clinical studies in the Gastro II department
• Transfer of project responsibilities to assigned employees

We are looking for a creative, ambitious, and collaborative EARLY-CAREER RESEARCHER to establish an independent junior research group () in TRANSLATIONAL GYNECOLOGIC CANCER RESEARCH, FOCUSING ON EARLY DETECTION, DIAGNOSIS, THERAPY, OR PREVENTION OF OVARIAN AND/OR ENDOMETRIAL CANCER AND OTHER...

• Use MINFLUX microscopy to track proteins during their translocation into mitochondria.
• Establish labeling techniques to tag proteins for MINFLUX tracking.
• Isolate proteins and assemble protein complexes in vitro.
• Work in an interdisciplinary and international environment.

Általános orvosi munkakörbe tartozó feladatok teljes körű ellátása...

RESPONSIBILITIES: • Provide clinical care to students • Keep records in accordance with German law and regulations • Be aware of special needs, e.g. students with health issues and/or chronic conditions • Demonstrate familiarity with procedures in case of infectious diseases • Communicate...

Create high-quality, scientifically accurate, and compliant content aligned with client objectives with guidance Build knowledge of therapeutic areas, client products, competitors, and industry regulations Adapt writing styles across various project types, formats and audiences Participate in...

Lead quality initiatives, processes and oversight of customer service / service recovery responses, in partnership with the in-country teams....

• The DPL and IDT ensure that the project is advanced in a scientifically sound, efficient, and regulatory-compliant manner, with optimal use of resources
• The DPL should possess a broad, cross-functional skill set and act less as a subject matter expert (SME) in a single area

• Preparation of analytical evaluation protocols
• Data evaluation (internal / external performance data) by using statistical tools
• Preparation of performance study reports
• Support the post-marked performance follow-up process
• Support the creation of templates for Clinical Evidence requirements

As a Senior Product Portfolio Manager (f/m/x) within ZEISS Meditec AG, your role is similar to and in strong collaboration with product management for the single products contributing to your clinical workflow solution...

As a Product Portfolio Manager (f/m/x) within ZEISS Meditec AG, your role is similar to and in strong collaboration with product management for the single products contributing to your clinical workflow solution....