Egészségügy, gyógyszeripar állások, munkák Külföldön

• Lead and coordinate the cleanroom cleaning team
• Act as the site's Hygiene Responsible Person
• Ensure correct gowning and hygienic behavior, conduct training for new and existing employees
• Coordinate cleanroom garments and clothing supply

• USP process development and optimization using various bioreactor systems (Sartorius, Finesse, Cytiva)
• Transfer of processes to the GMP environment
• Support of general laboratory organization
• Participation in weekend duties as required
• Regular reporting in the form of written reports and presentations

HOW YOU WILL MAKE AN IMPACT • Provide education on all aspects on one technology of the device, device handling, implantation and troubleshooting techniques related to equipment, tools and products required for device implants including full certification for independent case support • Educate and...

Support the country's LT in the development and execution of multi-year strategic account plans tailored to customer needs; co-creating solutions and value propositions that elevate customer relationships....

Working independently in the areas of valve crimping, case management, pre-case planning, post-case management, 3 Mensio management, Therapy Awareness program management and clinical education programs...

• Host audits and inspections, ensuring compliance with internal and regulatory requirements
• Manage and support GMP/GCLP procedures, including qualification and periodic review of facility equipment
• Support vendor qualification procedures and maintain related documentation as needed

Embedded Software Engineer myLife Diabetes Care AG is a new, independent Medtech company specialising in the treatment of diabetes. We are developing the next generation of the YpsoPump. Join us to engineer miracles for patients with diabetes. We're looking for a skilled, energetic and dynamic...

Manager QA Operations & FvP (m/w) 100%...

CMC Program Lead (Biologics) -Try&Hire (a) As CMC Program Manager, you will play a key role in driving the Chemistry, Manufacturing, and Controls (CMC) strategy and execution for the company's lead biologic program. You will collaborate closely with external Contract Development & Manufacturing...

• Strategic distribution of embecta's product portfolio in the field of diabetes care
• Holistic care and further development of specialist practices, diabetes centres, clinics, and pharmacies
• Systematic analysis of the assigned accounts, including derivation of individual sales and development strategies

As a medical physicist, you will be responsible for operating imaging devices in both clinical and research contexts. Ensuring safety in handling radioactive materials and the use of X-rays is a primary responsibility, and an appointment as radiation protection officer is foreseen. A major function...

Johnson & Johnson MedTech is the world leader in the electrophysiology market: the diagnostic and treatment by catheter ablation of cardiac arrythmias. Our growth has enabled a relentless focus on talent development by providing many new opportunities for our employees to expand their knowledge and...

Scientist Quality Assurance (100%) INNOMEDICA IS A YOUNG NANOTECH COMPANY with around 40 employees, several promising drugs in preclinical and clinical development and its own clean room production. The pipeline is based on a liposomal delivery system and includes, in particular, parenteral drug...

Scientific oversight and coordination of preclinical and toxicology studies conducted in collaboration with CROs, academic partners, and scientific institutions - covering both GLP-regulated and exploratory/non‑GLP research...

Active contribution to international projects in the areas of reimbursement and market access, including coordination, analysis, and substantive input on strategic topics...

Global Scientific Manager - IBU Critical Care Become part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced...

• You are responsible for quality related topics like change control, deviations and/or complaints related to DS products at CMOs
• Define together with the CMO effective CAPAs and track the timely implementation

Provide comprehensive In-patient clinical case management for a patient where they will be completing status reports upon admission and whilst the patient remains admitted to the provider....

Legal Advisory: Provide expert legal advice and guidance to senior management and legal colleagues on European regulations, directives, and policies impacting the business, including REACH, CLP, MDR/IVDR, GMP guidelines, pharmaceutical and/or medical device law, regulations, and guidance related to...

Supporting the advanced development team on a variety of projects that entail design, manufacturing, and testing of prototypes necessary to arrive at proof of concept for a novel eye implant technology...