Assurer les opérations de Conditionnement (Barrière Stérile et étiquetage) des produits dans le respect des délais, qualité, quantité, des procédures, réglementations, règles d’hygiène, de sécurité et valeurs de l’entreprise
Assurer les opérations de production (nettoyage, conditionnement Zone) Atmosphère Contrôlé (ZAC), et/ou étiquetage)
Respecter les règles de mise en place sur son poste de travail (6S)
Respecter les règles d’hygiène et bonnes pratiques comportementales dans son environnement de travail, et du port des tenues / EPI associées
Veiller au fonctionnement correct et régulier des équipements utilisés, et réaliser les maintenances de premier niveau
Requirements
Nice to have: Montages complexes avec contrôle
Nice to have: Paramétrage des machines
Nice to have: Tests micro-biologiques des surfaces et environnements
Field Service Specialist providing technical expertise on TA Instruments' innovative product suite for customer laboratories across Pharmaceutical & Life Sciences, Chemical Materials, Clinical, Food, Environmental, Forensics, Academia and Government industries.
Locations (3)
Connecticut, United States
Rhode Island, United States
Massachusetts, United States
Responsibilities
Provides customer service, training, diagnoses and troubleshoots customer problems, assists with parts management issues
Repairs, installs, and uses all currently supported instrument models and accessories; gains limited knowledge of applications software; calibrates instruments for efficient performance
Prepares a variety of reports, logs and documentation of service and repair activities; prepares service reports for input to the product reliability report; maintains up-to-date manuals, service notes, drawings, and other materials needed for efficiency
Senior Quality Partner responsible for ensuring medical devices and IVDs meet internal and external quality standards, managing change control, nonconformities, product release, design transfer, and continuous process improvement.
Responsibilities
Review and approve changes in the manufacturing process and product maintenance
Evaluate and authorize project, product, and process documents and evidence
Process and approve nonconformities and ensure timely resolution
Lead or support cross-functional quality management projects
Provide expertise in QMS and process consulting
Requirements
Technical or natural science degree or equivalent long-term experience in a technical field
The Quality Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards.
Compensation
Salary Range: 30.000€ - 37.000€.
Responsibilities
Complete document control transactions.
Manage Customer complaint investigations and complete complaint documentation.
Facilitate CAPA and NCR investigations and may coordinate investigation documentation.
Review DHR’s and support batch record release.
Manage record retention practices within the site.
Prepares a variety of paperwork to document work in progress, completed work, and other vital tracking paperwork; submits required paperwork on a timely basis to department management
Establishes and maintains prompt professional communications with customers and internal resources
Requirements
Associates Degree in Chemistry, Engineering, Biology, or other science related field
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