drug safety specialist oldenburg

... Medical Care. freseniusmedicalcare.de Drug Safety Associate (m/w/d) befristet bis 28.02.2022 Innerhalb von ... erhält und aufrechterhält. Als Drug Safety Associate (m/w/d) übernehmen Sie die Registrierung von ... Art (Adverse Event (AE), Adverse Drug Reaction (ADR)) als auch die Eingabe von Arzneimittelrisiken ... Dokumentation von "Periodic Safety Update Report"-bezogenen, sowie fallbezogenen Compliancedaten Sie ... Ebenfalls unterstützen Sie den Drug Safety Manager administrativ bei der Pflege des Pharmacovigilance System Master ... Als Drug Safety Associate (m/w/d) erwarten wir eine abgeschlossene Berufsausbildung zur ...

Du bist Student? Du sprichst fließend Deutsch und Englisch? Du willst mehr über herausragende Health & Safety Teams erfahren? Dann bewirb Dich auf unser Praktikum im Bereich Health and Safety/ Gesundheitsmanagement (m/w/d)! Wir suchen nach zielstrebigen und engagierten Studenten für die Mitarbeit in einem absolut einzigartigen, ... (4 Monate) betragen. Unser Workplace Health & Safety Team fördert eine positive Sicherheitskultur und die Einhaltung der Amazon-Sicherheitsstandards. Wir kümmern uns um die Aufrechterhaltung einer sicheren Arbeitsumgebung mit dem Amazon Global Safety Program. Hierzu führen wir Schulungen durch und coachen unsere Mitarbeiter ...

... employment Next Steps: By completing the registration process after clicking on "Apply Now", you will speed up your invitation for an interview. Please note that our central recruiting team is responsible for selecting applicants. They will also call you to arrange an appointment (area code 0211). Health and safety are a top priority for all our activities - even more so in the current situation. We and our clients consult with medical and health experts on an ongoing basis and implement all recommended precautions on our premises to ensure the health of our employees and all other people. Your Contact Adecco Personaldienstleistungen GmbH ...

... Company Part of an international organisation, specialising in the production of APIs, Drug Products, and associated Packaging Services. A dedicated professional team ensure the highest ... GMP, translating into high-value products. Role Description As a Quality Assurance Specialist you will join the product complaints and surveillance department which is in charge of ... and clinical products. Responsibilities - Initiate and own product quality complaints, Safety quality investigations and product security investigations - Perform assessments in support of ...

The ideal candidate will possess: - Scientific background along with a medico-scientific university degree e.g. Life Science - Pharmaceutical research / drug safety experience in post-marketing environment - Comprehensive knowledge of global safety regulatory requirements and extensive knowledge of safety regulations pertaining to Germany - Working knowledge of European GVP and Regulations pertaining to Adverse Event Reporting - Effective communicator (written and oral); concise, accurate and business appropriate - Proven ability to work cross functionally - Teamwork and initiative - Excellent attention to detail and be able to demonstrate and ...

Responsibilities & key activities - Oprational IIT management according to client and external (legal) requirements - Tracking of IIT progress and filing of all relevant IIT documents (databases, document repositories) - Liaise closely with respective local Medical Affairs Teams, Regulators Affairs, Compliance and Drug Safety - Liaise with Global Medical Affairs Operations group - Establish local SOPs and Working procedures where needed Requirements - Strong interpersonal skills, be a team player and be willing to work in an environment where individual initiative and accountability to the team are required - Effective communicator: interpersonal ...

... standards. Identifying sources of error and interface problems as early as possible and eliminating them before there is a loss of quality. Supporting the specialist departments in risk assessments and accompanying FMEA's are therefore participating in the further development of our quality management system. The implementation and support of occupational safety inspections and audits as well as the implementation of trainings for our employees complete your area of responsibility. What you bring to the job: Technical studies (Bachelor) - e.g. B. Electrical engineering / electronics, mechatronics, manufacturing technology - or a ...

... plan to ensure the most effective information-sharing possible, while coordinating with the business units - Act as sparring partner to our technology and sales teams - Actively collaborating on the compilation of suitable marketing concepts and tools to underpin the product safety strategy (food safety ink portal) - Setting up and maintaining a slide library for specialist areas - Developing and implementing an advertising strategy, including advertising campaigns, and providing relevant information on media and platforms (especially for technological themes and content) - Planning, organising and performing photo shoots; establishing and ...

Ihre Aufgaben: Als Reliability / Safety Specialist sind Sie für das Radarsystem Airport Surveillance Radar - Next Generation (ASR NG) für folgende Tätigkeiten zuständig: - Umsetzen von Zuverlässigkeitsüberprüfungen und Anfertigen von -berichten - Erstellen von Analysen für Nachbarabteilungen, u. a. Logistik und Engineering - ... Relex)) Ihre Qualifikationen: - Erfolgreich abgeschlossenes Studium der Elektrotechnik oder Ingenieurwesen - Erste Berufserfahrung als Reliability / Safety Specialist ist wünschenswert - Kenntnisse in den Tools: - Isograph Workbench - Isograph Fault Tree+ - PTC Windchill Quality Solutions (former Relex) - Erfahrungen in folgenden ...

... auf einem hohen Praxisniveau. Wenn Sie derartige Praxiserfahrungen gewinnen konnten und Spaß haben einmal auf der Software-Herstellerseite zu arbeiten, dann sollten wir uns schnellstmöglich einmal kennenlernen. Eine absolute Vertraulichkeit Ihrer Kontaktaufnahme ist für uns selbstverständlich und sichern wir Ihnen bereits im Vorfeld zu. Als Dienstorte können Sie zwischen unserem Standort in Timmel (Gemeinde Großefehn / Landkreis Aurich) in Ostfriesland, unserem City-Office in Oldenburg (Oldb.) oder unserem süddeutschen Standort in Ebermannstadt (Landkreis Forcheim) in Bayern wählen. Wir freuen uns über Ihre Bewerbung und/oder Kontaktaufnahme.

... are responsible for staff development and report to the Senior VP In Vivo Pharmacology. You are an experienced Senior Scientist or Group Leader with strong, proven leadership skills. You have a proven track record of in vivo phamacology and drug expertise in the field of drug development. You earned your merrits either in an academic research facility, or in a biotech or pharmaceutical company. You are a specialist in the area of immunological / inflammatory diseases. You have experience in moving projects from target validation to the PDC stage and beyond. Furthermore you have an understanding of PK / PD and know how to apply it to find the ...

... company with an extensive geographic coverage in Europe. Services include laboratory medicine, medical imaging, histophathology, reproductive medicine and drug development services. Clients include public and private healthcare providers, county councils, general public, insurance companies and the pharmaceutical industry. ... the business. Profile: - Bilingual German/French (written and spoken) + English - University degree in economics/administration/HR - 5 years experience as HR Specialist or in a project development role - A solid background in project management methodology - A track record in improving performance - Driven, tenacious, curious ...

... are responsible for staff development and report to the Senior VP In Vivo Pharmacology. You are an experienced Senior Scientist or Group Leader with strong, proven leadership skills. You have a proven track record of in vivo phamacology and drug expertise in the field of drug development. You earned your merrits either in an academic research facility, or in a biotech or pharmaceutical company. You are a specialist in the area of immunological / inflammatory diseases. You have experience in moving projects from target validation to the PDC stage and beyond. Furthermore you have an understanding of PK / PD and know how to apply it to find the ...

... unmet medical needs and contribute science-based information - Supervise provision of information to the respective disease areas and product-specific training, enabling the sales representatives to understand and convey the scientific benefits of a brand appropriately - Close interactions with Regulatory Affairs and Drug Safety when needed: manage the impact of SAEs and help manage the customer accordingly when SAEs and unexpected AEs arise - Act as Therapeutic Area Consultant for all other departments outside of the medical team including health economy as well as sales and marketing: provide ongoing scientific and medical support - Give ...

... South Germany and with occasional presence at our client's Munich office. The Senior Regional Market Access Manager is a Market Access and Reimbursement specialist who works with a cross-functional team on regional level. This role will be responsible for all therapeutic areas and it will be a partner to public ... - Must have in depth understanding of growing influence of public accounts on pharmaceutical marketplace. - Familiarity with regional contracts, agreements and drug steering features on national and regional level required, as well as ability to analyze regional contracts/agreements/features in respect to their influence on ...

... responsible for the external manufacturing of drug product. As Manufacturing GMP Specialist, you are involved in all GMP-related activities for ... execution and follow-up actions of aseptic drug product manufacturing at the external drug product manufacturing sites. You work with different ... Organizing drug product distribution to the different storage and clinical facilities; Keeping the oversight of the drug product inventory; ... - At least 4 years of experience in QA or aseptic drug product manufacturing is required, experience in (bio-) pharma industry is ...

Als bundesweit agierende Personalberatung suchen wir im Auftrag führender Arbeitgeber in den verschiedensten Branchen Fach- und Führungskräfte. Unser Kundenunternehmen ist erfolgreich in der der Personaldienstleistungsbranche tätig und hat uns mit der Suche nach einem erfahrenen Recruiter in Oldenburg beauftragt. Das Angebot: - Eine Festeinstellung mit Entwicklungsperspektive - Ein starkes Vergütungspaket zzgl. Provisionszahlungen - Ein angenehmes Arbeitsklima und motivierte, sympathische Kollegen - Transparente Strukturen, klare innerbetriebliche Kommunikation und gezielte Förderung Ihrer Stärken Ihre Aufgaben: - Sie beraten und pflegen den ...

... are responsible for staff development and report to the Senior VP In Vivo Pharmacology. You are an experienced Senior Scientist or Group Leader with strong, proven leadership skills. You have a proven track record of in vivo phamacology and drug expertise in the field of drug development. You earned your merrits either in an academic research facility, or in a biotech or pharmaceutical company. You are a specialist in the area of immunological / inflammatory diseases. You have experience in moving projects from target validation to the PDC stage and beyond. Furthermore you have an understanding of PK / PD and know how to apply it to find the ...