Job Title: Product Support InvestigatorLocation: DundeePay rate: £12.83Work days: Mon-FriShift Pattern: 08:30 - 16:30 Main Purpose of Role:The Product Support Investigator is responsible for logging, assessing the reportability of end-user complaints, and conducting investigations in accordance with site procedures and regulations.Main Responsibilities:Log, acknowledge, and assess alleged product deficiencies from end users for adverse event reportability
Job Title: Product Support InvestigatorLocation: DundeePay rate: £12.83Work days: Mon-FriShift Pattern: 08:30 - 16:30 Main Purpose of Role:The Product Support Investigator is responsible for logging, assessing the reportability of end-user complaints, and conducting investigations in accordance with site procedures and regulations.Main Responsibilities:Log, acknowledge, and assess alleged product deficiencies from end users for adverse event reportability
For our client, an international company in Solothurn, we are looking for a Senior QA Release LeadStart date: 01.05.2024End: 31.12.2024Extension: must be discussedWorkplace: BaarWorkload: 100%Job SummaryAct as Responsible Person (RP) delegate for Commercial Biologics Drug Substances (DS), Parenteral Drug Products (DP), Parenteral Finished Goods (FG) technical release or Active Pharmaceutical Ingredients (API), Pharmaceutical Drug Products, Pharmaceuticals
For our client, an international company in Solothurn, we are looking for a Senior QA Release LeadStart date: 01.05.2024End: 31.12.2024Extension: must be discussedWorkplace: BaarWorkload: 100%Job SummaryAct as Responsible Person (RP) delegate for Commercial Biologics Drug Substances (DS), Parenteral Drug Products (DP), Parenteral Finished Goods (FG) technical release or Active Pharmaceutical Ingredients (API), Pharmaceutical Drug Products, Pharmaceuticals
Nous recherchons pour notre client, une société internationale basée à Neuchâtel, un analyste QC (en travail posté) pour un contrat de 24 mois.Date de début : ASAPContrat : d'une durée de 24 mois via RandstadProlongation : possibleLieu de travail : NeuchâtelCharge de travail : 100 %Informations Piquet et Shift:Horaire variables: pas d’horaires fixes, peuvent venir 6h et 9h, pause midi de 30 min ou 1h entre 11h et 14h, et peuvent partir entre 16h et 20h le
Nous recherchons pour notre client, une société internationale basée à Neuchâtel, un analyste QC (en travail posté) pour un contrat de 24 mois.Date de début : ASAPContrat : d'une durée de 24 mois via RandstadProlongation : possibleLieu de travail : NeuchâtelCharge de travail : 100 %Informations Piquet et Shift:Horaire variables: pas d’horaires fixes, peuvent venir 6h et 9h, pause midi de 30 min ou 1h entre 11h et 14h, et peuvent partir entre 16h et 20h le
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
We are currently seeking a Senior Quality System engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you.This is an open ended temporary contract.Please note this vacancy requires fluency in French. Your responsibilities:QMS:Participate to procedure creation and updateEnsures GMP, GDP rules are known, understood and respected
We are currently seeking a Senior Quality System engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you.This is an open ended temporary contract.Please note this vacancy requires fluency in French. Your responsibilities:QMS:Participate to procedure creation and updateEnsures GMP, GDP rules are known, understood and respected
We are currently seeking a Quality engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you.This is an open ended temporary contract.Please note this vacancy requires fluency in French. Your responsibilities:Ensures that adequate Quality support is provided to productions and to open projects /initiativesEnsures that Non Confor
We are currently seeking a Quality engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you.This is an open ended temporary contract.Please note this vacancy requires fluency in French. Your responsibilities:Ensures that adequate Quality support is provided to productions and to open projects /initiativesEnsures that Non Confor
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
Senior Packaging EngineerLocation: Canton of NeuchatelType of contract: temporary,open-endedIf you’d like to work in a dynamic and friendly environment in the medical devices field then this position is made for you !This position requires fluency in both French and English. Your responsibilities:Activity linked to Packaging Engineering / Project ManagementOrganize work in a common approach to projects.Ability to define objectives.Decisions on technical d
Senior Packaging EngineerLocation: Canton of NeuchatelType of contract: temporary,open-endedIf you’d like to work in a dynamic and friendly environment in the medical devices field then this position is made for you !This position requires fluency in both French and English. Your responsibilities:Activity linked to Packaging Engineering / Project ManagementOrganize work in a common approach to projects.Ability to define objectives.Decisions on technical d
For our client, an international company in Solothurn, we are looking for a Manufacturing Associate IVStart date: ASAPEnd: contract for 1 yearExtension: possibleWorkplace:SolothurnWorkload: 100%Please not that the position includes shift work : Shift work - 2 shift work / 5 shift work (with allowance)Job SummaryPerforms and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation proto
For our client, an international company in Solothurn, we are looking for a Manufacturing Associate IVStart date: ASAPEnd: contract for 1 yearExtension: possibleWorkplace:SolothurnWorkload: 100%Please not that the position includes shift work : Shift work - 2 shift work / 5 shift work (with allowance)Job SummaryPerforms and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation proto