Job Title: Medical Safety Analyst DevicesLocation: SittingbournePay Rate: £23-£30 per hourDuration: 12 MonthsResponsibilities:Process consumer complaints related to enteral feeding medical devices in accordance with applicable regulations.Collect, assess, and document medical device complaints and adverse events promptly and compliantly.Conduct follow-up calls with customers to gather additional details on adverse events and complaints.Code complaints usin
Job Title: Medical Safety Analyst DevicesLocation: SittingbournePay Rate: £23-£30 per hourDuration: 12 MonthsResponsibilities:Process consumer complaints related to enteral feeding medical devices in accordance with applicable regulations.Collect, assess, and document medical device complaints and adverse events promptly and compliantly.Conduct follow-up calls with customers to gather additional details on adverse events and complaints.Code complaints usin
For our client Merck in Aubonne, we are looking for a Expert Quality Compliance (m/f/d) for a period of 12 months.Your role: As member of the Quality System & Compliance group, you willParticipate in continuous improvement of the site Quality Systems and in daily operational activitiesSupport Risk Management activitiesSupport Quality monitoring and Performance metricsAct Key User and administrator of computerized Quality management systemsDispense training
For our client Merck in Aubonne, we are looking for a Expert Quality Compliance (m/f/d) for a period of 12 months.Your role: As member of the Quality System & Compliance group, you willParticipate in continuous improvement of the site Quality Systems and in daily operational activitiesSupport Risk Management activitiesSupport Quality monitoring and Performance metricsAct Key User and administrator of computerized Quality management systemsDispense training
Vous êtes à la recherche d’une entreprise pharmaceutique dynamique ? Vous souhaitez être au cœur de l'excellence opérationnelle et à garantir la qualité des produits ? Nous recherchons un(e) professionnel(le) passionné(e) pour occuper un poste polyvalent et stimulant de QA spécialisteBasé à MontheyPoste temporaire avec possibilité d'évolution sur un poste permanent Vos missions Revue des dossiers de production et préparation du release : Travailler main da
Vous êtes à la recherche d’une entreprise pharmaceutique dynamique ? Vous souhaitez être au cœur de l'excellence opérationnelle et à garantir la qualité des produits ? Nous recherchons un(e) professionnel(le) passionné(e) pour occuper un poste polyvalent et stimulant de QA spécialisteBasé à MontheyPoste temporaire avec possibilité d'évolution sur un poste permanent Vos missions Revue des dossiers de production et préparation du release : Travailler main da
Do you consider yourself to be an organised individual, with great communication skills? Are you able to work effectively to provide procedural reports and updates? If so, we are looking for an individual who would be interested in joining a UK EHS Commercial Manager. You will be responsible for a number of tasks from supporting issues or incidents, conducting reviews and chairing committee meetings.Role details:Title - UK EHS Commercial ManagerLocation -
Do you consider yourself to be an organised individual, with great communication skills? Are you able to work effectively to provide procedural reports and updates? If so, we are looking for an individual who would be interested in joining a UK EHS Commercial Manager. You will be responsible for a number of tasks from supporting issues or incidents, conducting reviews and chairing committee meetings.Role details:Title - UK EHS Commercial ManagerLocation -
Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working
Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working
Pour notre client spécialisé dans les technologies médicales, englobant divers secteurs chirurgicaux tels que l'orthopédie, la neurochirurgie, la chirurgie générale et reconstructive, nous recherchons un(e) :Ingénieur/technicien en Lean Manufacturing (contrat temporaire indéterminé) Au sein du département d'amélioration continue vous intervenez en tant que professionnel en Lean manufacturing.Vous possédez une expertise dans la gestion des fournisseurs car
Pour notre client spécialisé dans les technologies médicales, englobant divers secteurs chirurgicaux tels que l'orthopédie, la neurochirurgie, la chirurgie générale et reconstructive, nous recherchons un(e) :Ingénieur/technicien en Lean Manufacturing (contrat temporaire indéterminé) Au sein du département d'amélioration continue vous intervenez en tant que professionnel en Lean manufacturing.Vous possédez une expertise dans la gestion des fournisseurs car
Are you ready to dive into the world of Regulatory Affairs and Quality Assurance ? We're on the lookout for a RA & QA Compliance Specialist to join a dynamic team and medical device company ! We are seeking a qualified candidate for the role of Regulatory Affairs and Quality Assurance Specialist. This position is integral to ensuring compliance with the EU Medical Device Regulation (EU MDR), Swiss Medical Devices Ordinance (Swiss MedDO), and relevant regul
Are you ready to dive into the world of Regulatory Affairs and Quality Assurance ? We're on the lookout for a RA & QA Compliance Specialist to join a dynamic team and medical device company ! We are seeking a qualified candidate for the role of Regulatory Affairs and Quality Assurance Specialist. This position is integral to ensuring compliance with the EU Medical Device Regulation (EU MDR), Swiss Medical Devices Ordinance (Swiss MedDO), and relevant regul