Provide advanced aesthetic treatments to enhance skin health and improve facial and body appearance. Perform non-surgical procedures, assess client needs, recommend suitable treatments, ensure safety standards, and deliver high quality patient care.

In order to work in Ireland a non-EEA National, unless they are exempted, must hold a valid employment permit. Please review the Eligibility and requirements for an employment permit if you are unsure of your eligibility to apply for this vacancy.
Scope of the role The role of the Medical Technical Assistant is to work, in co-operation with the Medical Director and laboratory management, as part of a team in the provision of diagnostic laboratory services in accordance with company policies. You will actively contribute to the operation of a quality management system in compliance with ISO15189 INAB standards and cooperate with the Laboratory Manager(s) and with other senior personnel in training staff as required. Roles and Responsibilities -Assist in the preparation and processing of patient samples for analysis, ensuring adherence to laboratory protocols and quality standards. -Operate and maintain laboratory instruments, including setting up, calibrating, and troubleshooting equipment as necessary. -Perform routine and specialised laboratory techniques under the supervision of senior laboratory staff. -Maintain and manage laboratory instruments, ensuring they are clean, functional, and ready for use. Perform regular checks and routine maintenance as required. -Assist in the development and validation of new laboratory methods, under the guidance of senior scientists or laboratory management. -Monitor inventory levels of laboratory supplies and reagents, ensuring adequate stock for laboratory operations. -Participate in quality control procedures to ensure the accuracy and reliability of laboratory results. Document and report any discrepancies or issues in accordance with laboratory protocols. -To treat patients, their personal data and their samples with due care and respect. -Strictly adhere to laboratory safety protocols and procedures, ensuring a safe working environment for all laboratory staff. -Participate in safety audits and contribute to the continuous improvement of laboratory safety practices. -Participate in ongoing training to enhance technical skills and laboratory knowledge, with a focus on advancing towards a Medical or Clinical Scientist role. -Work closely with the sample receipt team and Medical Laboratory Aides (MLAs) to ensure the seamless transfer of samples from the receipt room to the laboratory. -Collaborate with laboratory scientists and other technical staff to optimise laboratory workflows and enhance overall efficiency. -Undertake any other laboratory-related tasks or projects as directed by laboratory management, contributing to the overall success of the laboratory team. Qualifications and Experience -A 3rd level science qualification in a relevant subject OR minimum of 1 year relevant work experience as Medical Laboratory Aide (MLA). -Further qualification(s) in any laboratory discipline, clinical laboratory experience or work in an accredited environment is desirable but not essential as full training will be provided. -Able to work both independently and as part of a team. -Good analytical, critical thinking and problem-solving skills.

We are building a team of dedicated individuals who want to grow with us- offering care, support, and assistance to people who rely on us for essential daily needs.

Ein etabliertes Unternehmen im Bereich Medizintechnik / regulierte Produktion sucht zur Verstärkung des Produktionsteams einen engagierten Assembler. Ziel der Position: Sicherstellung der qualitäts‑ und termingerechten Montage von medizintechnischen Instrumenten und Baugruppen unter Einhaltung aller Qualitäts‑, Sicherheits‑ und regulatorischen Vorgaben (z. B. GMP, ISO 13485). Ihre Aufgaben: • Montage und Inbetriebnahme von Instrumenten und Baugruppen nach Arbeitsanweisungen • Durchführung von Sicht‑ und Funktionsprüfungen • Dokumentation der Arbeitsschritte gemäss Qualitätsmanagement‑Vorgaben • Einhaltung von Qualitäts‑, Umwelt‑ und Sicherheitsrichtlinien (EHS, GMP) • Sorgfältiger Umgang mit Materialien, Bauteilen, Werkzeugen und Prüfmitteln • Meldung von Abweichungen, Fehlern oder Verbesserungsvorschlägen • Mitarbeit bei kontinuierlichen Verbesserungsprozessen (KVP) • Unterstützung bei 5S‑Aktivitäten sowie Ordnung und Sauberkeit am Arbeitsplatz • Mitwirkung bei der Schulung anderer Mitarbeitender • Bereitschaft zu Samstagsarbeit, Schichtarbeit und Teamwechsel je nach Auslastung Ihr Profil: • Abgeschlossene technische Berufsausbildung (EFZ) • Sehr gute Deutschkenntnisse in Wort und Schrift • Grundkenntnisse im Umgang mit Computer und MS Office • Strukturierte, zuverlässige und qualitätsbewusste Arbeitsweise • Teamfähigkeit, Flexibilität und Lernbereitschaft • Bereitschaft zur Arbeit an einem Steharbeitsplatz Von Vorteil • Erste Erfahrung in einem technischen oder produzierenden Umfeld • Kenntnisse in GMP‑ oder ISO‑regulierter Produktion • Erfahrung mit MRP‑ oder SAP‑Systemen • Grundkenntnisse Englisch

What are you looking for? Loading component... Medical Monitoring High quality oversight for safety and compliance. Expert medical monitoring is crucial for streamlining clinical research. An integrated approach will improve outcomes while ensuring trial subject safety. We offer unrivaled expertise in medical monitoring services, providing tailored solutions in accordance with study specifications and requirements. Our safety physicians have extensive knowledge of a broad range of therapeutic areas and will support essential project oversight and procedure clarity, enabling close interaction with key partners and timely delivery of evaluations. We also offer support for smooth patient recruitment, ensuring safety and helping you to define and qualify inclusion/exclusion criteria. Our experts provide high-quality medical review services for study protocols, clinical study reports, review and approval of MedDRA and ATC codes, as well as medical reviews of a wide range of safety data, including adverse effects (AEs) and serious adverse effects (SAEs) reported in the clinical and/or safety database. Additional services include independent medical monitoring for safety review meetings and participation in Independent Data Monitoring Committees (IDMCs) and Data Safety Monitoring Boards (DSMBs). SGS is recognized as the benchmark for quality and integrity in clinical research. We are your first choice when looking for exceptional customized medical monitoring for your research project.

Medical Advisor - Location: Amsterdam, Netherlands - Contact: Stefan Charles - Job type: - Contact phone: +31 (0)20 406 97 50 - Industry: Clinical Research - Contact email: stefan_charles@oxfordcorp.com Our client operates within the global pharmaceutical industry and focuses on clinical research and the development of innovative therapies. Working in a highly regulated and collaborative environment, the organization supports clinical studies that contribute to advancing healthcare. To strengthen the Clinical Study team, our client is seeking a Medical Advisor who can bridge science, operations, and stakeholders. Job Description As a Medical Advisor, you act as the medical and scientific expert within clinical trial activities. You support both local and international study teams by ensuring that research is conducted in line with regulatory standards and scientific best practices. The role involves advising on study designs, supporting feasibility assessments, and addressing medical questions that arise during trials. You collaborate with internal departments and external partners such as investigators and specialists, ensuring strong alignment between global strategies and local execution. You also contribute to documentation and support communication with regulatory authorities. Requirements - Medical degree preferred, or PhD/PharmD in life sciences. - Strong scientific knowledge and understanding of clinical development. - Experience in clinical practice, research, or pharmaceutical development. - Familiarity with ICH-GCP guidelines and regulatory frameworks. - Strong stakeholder management and communication skills. - Fluent in English. - Proactive, independent, and comfortable working in a dynamic environment. - Work visa required, and already situated in the Netherlands. If these requirements are not met you will not receive a response to your application

Institut AllergoSan

Arbeiten mit gutem Bauchgefühl.

Werden Sie Teil unserer Erfolgsgeschichte!

Das Institut AllergoSan ist mit seiner Marke OMNi-BiOTiC® seit Jahren die Nummer 1 am österreichischen und deutschen Probiotika-Markt sowie in über 40 Ländern weltweit vertreten. Denn 30 Jahre Erfahrung in der Erforschung und Entwicklung von Probiotika, pflanzlichen Wirkstoffen und orthomolekularer Medizin begeistert unsere Kunden und die verordnenden Ärzte. Qualität liegt in unserer DNA - dies bedeutet spürbare Wirksamkeit, sowie Anerkennung weltweit und damit Freude für jedes unserer Team-Mitglieder. 1 MEDICAL DIRECTOR M /W / D

Vollzeit - Graz

Zur Vergrößerung und Unterstützung unseres Teams suchen wir eine begeisterte und aufgeschlossene Persönlichkeit.

Schwerpunkte

>> Entwicklung und Umsetzung der Forschungsstrategie im Bereich Darm-Mikrobiom sowie von wirksamen Pro-, Prä- und Postbiotika

>> Gesamtverantwortung für die Planung, Steuerung und Umsetzung von Forschungsprojekten in interdisziplinären Teams aus Medizin, Biologie, Pharmazie und Biochemie

>> Repräsentation des Unternehmens durch die Präsentation wissenschaftlicher Ergebnisse auf nationalen und internationalen Fachkongressen sowie in wissenschaftlichen Publikationen

>> Aufbau, Pflege und strategische Erweiterung von Netzwerken in Wissenschaft, Industrie, Öffentlichkeit sowie innerhalb der Ärzte- und Apothekerschaft

>> Führung, Förderung und Weiterentwicklung des medizinisch-wissenschaftlichen Fachpersonals im Institut AllergoSan

>> Mitwirkung an strategischen und operativen Unternehmensentscheidungen aus wissenschaftlicher Perspektive

Anforderungsprofil

>> Managementpersönlichkeit mit einem akademisch geprägten Werdegang und praktischer Erfahrung in der Industrie oder einer Forschungseinrichtung

>> Promotion im Bereich Medizin, Pharmazie, Mikrobiologie oder verwandten Disziplinen

>> Vertiefte Expertise im Bereich Darmmikrobiom-Forschung und in der wissenschaftlichen Bewertung bzw. Anwendung von Probiotika ist von besonderem Vorteil

>> Mehrjährige Forschungserfahrung

>> Ausgeprägte Fähigkeit, komplexe, wissenschaftliche Inhalte verständlich und überzeugend zu vermitteln (Marketing-Mindset)

>> Gutes Netzwerk in Wissenschaft und/oder Industrie

>> Unternehmerisches Denken, Innovationsgeist, Empathie und Flexibilität

>> Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift

Benefits

>> Kostenlose Parkplätze oder Klimaticket Steiermark

>> Gleitzeit und Home-Office-Möglichkeit

>> Events und familiäres Setting

>> Geförderte Mahlzeiten

>> Gesundheits- & Sportangebote

>> OMNi-BiOTiC®-Bar und viele Goodies

Gehalt

Für diese Position gilt ein Mindestbruttoentgelt von € 5.357,- auf Vollzeitbasis. Unser attraktives Gehaltspaket liegt jedoch über dem angegebenen Mindestgehalt.

JETZT BEWERBEN

Bitte laden Sie Ihre Bewerbungsunterlagen auf unserem Bewerbungsportal unter folgendem Link hoch:

https://www.allergosan.com/at/karriere/?jh=gr5bfi41rwfhv9tdoy3oj6syt469z53

Wenn Sie uns zusätzlich Ihr Porträtfoto oder ein kurzes Video übermitteln möchten, freuen wir uns, ein Gesicht zu Ihrer Bewerbung zu erhalten.

Ansprechpartnerin:

Magdalena Wallner, BA

Tel.: +43 (0)316 405 305 141

www.omni-biotic.com

https://www.allergosan.at Das Mindestentgelt für die Stelle als MEDICAL DIRECTOR M /W / D beträgt 5.357,00 EUR brutto pro Monat auf Basis Vollzeitbeschäftigung. Bereitschaft zur Überzahlung.

FMTC logo Amsterdam - Instructor Medical Frist Aid & Medical Care - On-site - - Amsterdam , Noord-Holland , Netherlands - €2,800 - €4,000 per month Job description Do you thrive on inspiring others, sharing knowledge, and making a real impact through hands-on training? Are you someone who takes ownership, embraces variety, and feels at home in an international and fast-moving environment? Who Are We? At FMTC Safety, everything revolves around people and safety. We are a fast-growing, global organization preparing professionals to work safely in some of the world's most demanding environments: from offshore platforms and wind farms to ships and industrial sites. Job requirements You don't just deliver courses, you create impactful learning experiences that truly prepare people for real-life offshore emergencies. What will you do? No two days are the same and that's exactly what excites you. You take full ownership of your trainings and: Why FMTC? Because here, you don't just join a company, you become part of a journey.

Senior Medical Writer (m/w/d) Are you looking for a full-time position in a pan-European strategic consultancy as a Senior Medical Writer to streamline patient access to life-changing treatments through expert guidance, innovative tools, and impeccable delivery? Location: Hybrid with office in Hannover & regular in-person presenceSalary: Competitive, based on experience We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC), a pan-European specialist consultancy that partners with ambitious health technology developers through the complex journey to achieve successful market access across Europe, with our tailored approach, global perspective and local expertise. Our clients in healthcare and life sciences are leading innovators in pharma, biotech, medtech, digital health, and diagnostics. As part of Kintiga, we support the successful launch and reimbursement of breakthrough therapies and technologies. Join our team and help shape the future of the cutting-edge healthcare solutions. At Kintiga, we cultivate a collaborative and entrepreneurial culture where every voice matters. We value diversity, openness, and integrity - encouraging our team members to bring their ideas and passion to work every day. Become part of a supportive, dynamic team that thrives on innovation, lifelong learning, and making a meaningful impact in healthcare and life sciences. How you will create an impact As Senior Medical Writer at Kintiga, you will take on a leading role in the content and organizational delivery of market access projects. You will act as a key contact for clients, manage timelines and resources, and contribute to the strategic direction and quality of projects. In addition, you will support team development through coaching, training, and the continuous advancement of methods and best practices, thereby helping to drive sustainable project success and organizational growth. - Act as end-to-end Project Lead / Product Owner, ensuring high-quality delivery across content, timelines, risks, budgets, and cross-functional workstreams - Develop and execute medical and market access strategies, including HTA dossier strategy, market access risk assessments, and strategic positioning for price negotiations - Lead G-BA advice meetings, Joint Scientific Consultations (JSC), and the development, preparation, and submission of AMNOG and JCA dossiers in close collaboration with clients - Collaborate in and promote interdisciplinary, agile teams, applying modern working methods and driving continuous improvement - Support business development activities, including proposal development and opportunity identification - Actively contribute to knowledge sharing, internal capability building, mentoring, and cultural development About you: - Master’s degree in life sciences, medicine, pharmacy, health economics, or a related field - 1–3 years of professional experience in the pharmaceutical industry and/or market access or management consulting - Good knowledge of the German healthcare system and the AMNOG process, including experience with benefit dossiers - Strong skills in scientific literature research and medical writing - Experience in project management, as well as conducting and moderating trainings and workshops - Native level German and excellent English language skills (C2), both written and spoken - Strong analytical, structured, and detailoriented working style with a high level of independence and reliability - Confident communication and presentation skills, including the ability to explain complex topics clearly - Agile mindset with an understanding of modern working methods and the Product Owner role - Committed, flexible team player with enthusiasm for complex topics and willingnes to travel occasionally across Europe What we offer on top: - Competitive Salary (dependent on experience) - Extensive benefit programme - Company-wide meet-ups - International work environment with cross-border responsibilities - Generous annual leave entitlement - Hybrid environment – a mixture of office and home working - Flexible working – to help maintain a better work/life balance We bring together diverse backgrounds and expertise, and our team is dynamic, solutions-focused, and committed to delivering excellence. If you are a results-driven Medical Writer professional looking for an opportunity to help shape the future of a growing business, we'd love to hear from you! Sounds good to you? Apply now! We look forward to receiving your application, incl. - Letter of application - Curriculum vitae - Complete certificates incl. high school diploma - Earliest possible start date - Salary expectations Please submit your application via ouronline application portal (https://kintiga.bamboohr.com/careers/91?source=aWQ9MTM%3D) .

In order to work in Ireland a non-EEA National, unless they are exempted, must hold a valid employment permit. Please review the Eligibility and requirements for an employment permit if you are unsure of your eligibility to apply for this vacancy.
Post ID: 039273 Post Summary:- The Discipline of Medical Education in the School of Medicine at Trinity College invites applications for the post of Assistant Professor in Medical Education with a particular focus on clinical education, the development of high-quality clinical learning experiences for students, and the building of networks of clinical educators across partner healthcare sites. The postholder will play a key role in the design, delivery, evaluation and enhancement of workplace-based learning across the undergraduate and internship continuum, ensuring alignment with university policy, international best practice, and the standards of the Irish Medical Council. The successful applicant will have an established or emerging reputation in teaching, faculty development, and educational scholarship, and will contribute to curriculum review with particular emphasis on clinical placements, longitudinal integrated clerkships, internship preparation, and transitions into postgraduate training. Appointees will divide their time between teaching, educational research, and leadership of initiatives that support clinical supervisors, clinical tutors, and teaching hospitals in delivering excellent learning experiences. The postholder will play a critical role in strengthening partnerships between the School of Medicine and its affiliated clinical sites, and in developing sustainable communities of practice among clinical educators. Post status: 2 Year Fixed-Term Contract This employment is for the specific purpose of supporting the development of clinical placements across affiliated sites and delivering identified short- to medium-term strategic objectives in medical education and clinical training. This employment is not offered on an indefinite duration basis as it is aligned to a fixed-term requirement to support curriculum reform and the development of clinical education initiatives within the School of Medicine. Hours of Post: Hours of work for academic staff are those as prescribed under Public Service Agreements. For further information please follow the link below: http://www.tcd.ie/hr/assets/pdf/academic-hours-public-service-agreement.pdf Salary: This appointment will be made on the Assistant Professor Salary Scale (€43,859 - €104,618 per annum) at a point in line with current Government pay policy. monthly/weekly payscales. (tcd.ie) Closing Date: 12 Noon Irish Standard Time, 4th August 2026 How to apply: To assist the selection process, applicants should submit; Cover Letter (1x A4 page) A comprehensive curriculum vitae, including a full list of publications The names and contact details (i.e. addresses, e-mail, etc.) of three referees A comprehensive research plan (maximum 2 pages) and a teaching statement (maximum 2 pages) Please note: Applicants who do not submit the above will not be considered at the short list stage Applicants should note that the interview process for this appointment will include the deliver