Eurofins

Unfortunately we are unable to offer visa sponsorship for this role.This is a permanent full time position working a 35 hour week 7 hours per day flexibly between 7am & 7 pm on 5/7 days as per business needs.  The purpose of this job is to perform analysis of pharmaceutical raw materi

Unfortunately we are unable to offer visa sponsorship for this role.This is a permanent full time position working a 35 hour week 7 hours per day flexibly between 7am & 7 pm on 5/7 days as per business needs.  The purpose of this job is to perform analysis of pharmaceutical raw materi

Eurofins BioPharma Product Testing ricerca per la propria sede di Vimodrone (MI) un/a laureato/a da inserire in stage nel proprio reparto Quality Assurance. La risorsa dovrà collaborare con il QA Manager alla gestione della documentazione cambi deviazioni e CAPA.Il ruolo non prevede a

Eurofins BioPharma Product Testing ricerca per la propria sede di Vimodrone (MI) un/a laureato/a da inserire in stage nel proprio reparto Quality Assurance. La risorsa dovrà collaborare con il QA Manager alla gestione della documentazione cambi deviazioni e CAPA.Il ruolo non prevede a

Working in Eurofins BPT Toronto you will provide preparing Quotations to present to Business Development or to the Senior Management for onward submissions to the clients. Principal Duties & Responsibilities:Organize prioritize and provide accurate and timely delivered quotations requ

Working in Eurofins BPT Toronto you will provide preparing Quotations to present to Business Development or to the Senior Management for onward submissions to the clients. Principal Duties & Responsibilities:Organize prioritize and provide accurate and timely delivered quotations requ

The Laboratory IT Support Technician is responsible for maintaining the Laboratory Information Management System (LIMS) configuration and supporting day-to-day laboratory IT needs. This role includes but is not limited to creating analytical packages custom test lists and updating reg

The Laboratory IT Support Technician is responsible for maintaining the Laboratory Information Management System (LIMS) configuration and supporting day-to-day laboratory IT needs. This role includes but is not limited to creating analytical packages custom test lists and updating reg

Key ResponsibilitiesProduct Design & ArchitectureLead the design and architecture of complex software products built on the .NET ecosystem.Translate business requirements into scalable technical designs ensuring alignment with enterprise architecture standards.Define product technical

Key ResponsibilitiesProduct Design & ArchitectureLead the design and architecture of complex software products built on the .NET ecosystem.Translate business requirements into scalable technical designs ensuring alignment with enterprise architecture standards.Define product technical

Prise en charge des échantillons et effectuer les ensemencements incubations et lectures selon les normes / procédures en vigueurLecture des résultatsEntrée des résultats dans le LIMSPréparation des milieux de culture réactifs et solutionsGestion des déchets biologiques selon procédur

Prise en charge des échantillons et effectuer les ensemencements incubations et lectures selon les normes / procédures en vigueurLecture des résultatsEntrée des résultats dans le LIMSPréparation des milieux de culture réactifs et solutionsGestion des déchets biologiques selon procédur

Als Mitarbeiter (m/w/d) Probeneingang Logistik nimmst Du die tägliche Probenanlieferung entgegen und priorisierst sie entsprechend unserer Vorgaben.Dabei übernimmst Du selbstständig die Eingangskontrolle der angelieferten Proben (Boden Bausubstanz Wasser Abwasser) auf Plausibilität un

Als Mitarbeiter (m/w/d) Probeneingang Logistik nimmst Du die tägliche Probenanlieferung entgegen und priorisierst sie entsprechend unserer Vorgaben.Dabei übernimmst Du selbstständig die Eingangskontrolle der angelieferten Proben (Boden Bausubstanz Wasser Abwasser) auf Plausibilität un

Som Key Account Manager Drinking- & Coastal Water bliver du den der kombinerer faglig indsigt med tillidsskabende dialoger. Du trives i rollen som rådgiver der både kan skabe nye relationer og sikre at kunderne oplever høj kvalitet og gennemsigtighed i samarbejdet. Du er nysgerrig ana

Som Key Account Manager Drinking- & Coastal Water bliver du den der kombinerer faglig indsigt med tillidsskabende dialoger. Du trives i rollen som rådgiver der både kan skabe nye relationer og sikre at kunderne oplever høj kvalitet og gennemsigtighed i samarbejdet. Du er nysgerrig ana

Logs and tracks the receipt and shipment of all samples into and out of the Service Center and verifies receipt of samples. Assists in preparing bottle kits for delivery to clients and ensures accurate and timely documentation of sample log in labeling and routing. Determines the prio

Logs and tracks the receipt and shipment of all samples into and out of the Service Center and verifies receipt of samples. Assists in preparing bottle kits for delivery to clients and ensures accurate and timely documentation of sample log in labeling and routing. Determines the prio

Eurofins Environment Testing Southwest- Tustin CA is searching for a SVOA GCMS Chemist I to prepare and analyze environmental samples following EPA protocols in adherence with Eurofins Quality Assurance programs and SOPs.Chemist / Analyst duties will include but are not limited to the

Eurofins Environment Testing Southwest- Tustin CA is searching for a SVOA GCMS Chemist I to prepare and analyze environmental samples following EPA protocols in adherence with Eurofins Quality Assurance programs and SOPs.Chemist / Analyst duties will include but are not limited to the

Job Summary: Eurofins BPT-Columbia is looking for a Sr. Scientist to join our team located in Columbia Missouri. This individual will be a subject matter expert in testing Drug Substances and Drug Products in the Biotech department. The successful candidate will perform method establi

Job Summary: Eurofins BPT-Columbia is looking for a Sr. Scientist to join our team located in Columbia Missouri. This individual will be a subject matter expert in testing Drug Substances and Drug Products in the Biotech department. The successful candidate will perform method establi

About the RoleWe have an exciting opportunity for a Robotics/Automation Engineer with a strong background in pharmaceutical laboratory experience to join a growing team at a PSS client site. This role focuses on building operating and maintaining automated liquid handling and robotic

About the RoleWe have an exciting opportunity for a Robotics/Automation Engineer with a strong background in pharmaceutical laboratory experience to join a growing team at a PSS client site. This role focuses on building operating and maintaining automated liquid handling and robotic

Eurofins Environment Testing is seeking a Sample Control Technician to join our Team in Tustin CA!Sample Control Technician responsibilities include but are not limited to:Perform all duties as outlined in the Standard Operating Procedure for Sample Control Technicians.Receive log in

Eurofins Environment Testing is seeking a Sample Control Technician to join our Team in Tustin CA!Sample Control Technician responsibilities include but are not limited to:Perform all duties as outlined in the Standard Operating Procedure for Sample Control Technicians.Receive log in

Location: Baltimore MD This position requires working on-site at our Baltimore office 5 days per week with up to 25% travel to company sites (typically one week per month).Position Overview:The Systems Administrator is a key IT professional responsible for the configuration managemen

Location: Baltimore MD This position requires working on-site at our Baltimore office 5 days per week with up to 25% travel to company sites (typically one week per month).Position Overview:The Systems Administrator is a key IT professional responsible for the configuration managemen

General Responsibilities:Responsible for performing a variety of tasks in support of the daily production of sterile cell therapy products. Tasks are predominately performed within a cleanroom environment under current Good Manufacturing Practices (cGMP) conditions.Responsibilities:Pr

General Responsibilities:Responsible for performing a variety of tasks in support of the daily production of sterile cell therapy products. Tasks are predominately performed within a cleanroom environment under current Good Manufacturing Practices (cGMP) conditions.Responsibilities:Pr

Perform cGMP Microbial testing (Environmental Monitoring Gas Monitoring)Execute phase-appropriate test method validation protocols as neededSupport operational systems (equipment/instrument maintenance/calibration equipment alarm monitoring sample handling/tracking cGMP documentation

Perform cGMP Microbial testing (Environmental Monitoring Gas Monitoring)Execute phase-appropriate test method validation protocols as neededSupport operational systems (equipment/instrument maintenance/calibration equipment alarm monitoring sample handling/tracking cGMP documentation

The Quality Assurance Specialist is responsible to support the Quality Assurance department and laboratory staff; assist with the certification processes (renewals scope additions Proficiency Test Sample tracking and reporting etc.); process laboratory and client requests for informat

The Quality Assurance Specialist is responsible to support the Quality Assurance department and laboratory staff; assist with the certification processes (renewals scope additions Proficiency Test Sample tracking and reporting etc.); process laboratory and client requests for informat

We are seeking a motivated and detail-oriented Biochemistry Team Lead with at least 2 years of relevant laboratory experience to join our team. This role combines hands-on technical expertise with leadership responsibilities supporting the characterization of early-stage biotherapeuti

We are seeking a motivated and detail-oriented Biochemistry Team Lead with at least 2 years of relevant laboratory experience to join our team. This role combines hands-on technical expertise with leadership responsibilities supporting the characterization of early-stage biotherapeuti

The Quality Assurance (QA) Specialist is responsible for performing internal audits assisting with external audits overseeing the maintenance of QC records certifications review and revision of Standard Operating Procedures (SOPs) training records Demonstrations of Capability (DOCs) a

The Quality Assurance (QA) Specialist is responsible for performing internal audits assisting with external audits overseeing the maintenance of QC records certifications review and revision of Standard Operating Procedures (SOPs) training records Demonstrations of Capability (DOCs) a

Responsible for performing a variety of tasks in support of the daily production of sterile cell therapy products. Tasks are predominantly performed within a cleanroom environment under current Good Manufacturing Practices (cGMP) conditions.Responsibilities:Proficient in aseptic techn

Responsible for performing a variety of tasks in support of the daily production of sterile cell therapy products. Tasks are predominantly performed within a cleanroom environment under current Good Manufacturing Practices (cGMP) conditions.Responsibilities:Proficient in aseptic techn