Lavori attuali relativi a Qc Biochemical Documentation Officer - Monza, Lombardia - Thermo Fisher Scientific
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Documentation Officer
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QC Equipment Calibration Specialist
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Monza, Lombardia, Italia Thermo Fisher Scientific A tempo pieno{"title": "QC NPI Compliance Specialist", "description": "Job SummaryWe are seeking a highly organized and detail-oriented QC NPI Compliance Specialist to join our team at Thermo Fisher Scientific. The successful candidate will be responsible for managing the documentation, reordering, and correct storage of Reference Standards and reagents in the DPS...
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QC Equipment Calibration Specialist
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QC Equipment Calibration Specialist
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QC Equipment Calibration Specialist
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Monza, Lombardia, Italia Tn Italy A tempo pienoJob Summary:We are seeking a highly skilled QC Equipment Calibration Specialist to join our team at Tn Italy. As a key member of our Quality Control Function, you will be responsible for ensuring the correct calibration and maintenance status of our laboratory equipment.Main Responsibilities:Execute daily calibration activities to ensure equipment accuracy...
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QC Equipment Calibration Specialist
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Monza, Lombardia, Italia Thermo Fisher Scientific A tempo pienoAbout Thermo Fisher ScientificAt Thermo Fisher Scientific, we're dedicated to working the right way, for the right reasons. Our team is passionate about making a difference in the world, and we're committed to providing the resources and opportunities our colleagues need to succeed.Our MissionWe enable our customers to make the world healthier, cleaner, and...
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QC Equipment Calibration Specialist
2 settimane fa
Monza, Lombardia, Italia Thermo Fisher Scientific A tempo pienoAbout Thermo Fisher ScientificAt Thermo Fisher Scientific, we're dedicated to working the right way, for the right reasons. Our team is passionate about making a difference in the world, and we're committed to providing the resources and opportunities our colleagues need to succeed.Our MissionWe enable our customers to make the world healthier, cleaner, and...
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Analytical Development Specialist
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Analytical Development Specialist
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Pharmaceutical Development Specialist
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Analytical Development Specialist
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Monza, Lombardia, Italia Thermo Fisher Scientific A tempo pienoAbout the RoleWe are seeking a highly skilled Quality Control Documentation Expert to join our team at Thermo Fisher Scientific. As a key member of our PDS Analytical Development & GMP Department, you will be responsible for ensuring the successful continuation of projects within the department.Key ResponsibilitiesDevelop and maintain accurate and compliant...
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Calibration Specialist for Quality Control Equipment
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Monza, Lombardia, Italia Thermo Fisher Scientific A tempo pienoJoin a Leader in Scientific Innovation: At Thermo Fisher Scientific, we are committed to making a difference in the world through our innovative work and dedication to customer satisfaction. Our mission is to enable our customers to create a healthier, cleaner, and safer world. We are the largest player in the industry, with a strong focus on research and...
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Monza, Lombardia, Italia Thermo Fisher Scientific A tempo pienoJoin a Leader in Scientific Innovation: At Thermo Fisher Scientific, we are committed to making a difference in the world through our innovative work and dedication to customer satisfaction. Our mission is to enable our customers to create a healthier, cleaner, and safer world. We are the largest player in the industry, with a strong focus on research and...
Qc Biochemical Documentation Officer
3 mesi fa
Entrerai a far parte del team QC Biochemical Laboratory, e supporterai la start up di una nuova unità dedicate alla produzione di mRNA. In particolare ti occuperai di:
- Revisione delle procedure operative standard e relativa documentazione associata in Documentum;
- Scrittura di Change control, Deviazioni, Indagini di laboratorio, OOS, SST failure tramite sistema Global TrackWise;
- Scrittura ed emissione dei metodi analitici e degli Analytical Test Record per il laboratorio, interfacciandosi con il reparto Regulatory Affair;
- Scrittura di protocolli e report analitici;
- Apertura delle classi a sistema per il team tramite il sistema Success Factor;
- Scrittura e revisione delle specifiche regolatorie per la parte Quality Control;
- Altre attività di supporto correlate secondo necessità.
REQUISITI:
- Laurea in discipline scientifiche (CTF, Biologia, Biotecnologie..)
- Esperienza di almeno 1 anno in realtà farmaceutiche/biotech in ambito documentale
- Esperienza all'interno di un laboratorio di Quality Control GMP e con i principali strumenti (es. HPLC)
- Buona conoscenza del pacchetto Office, buon uso del PC e dei sistemi informatici per la gestione della documentazione, buona conoscenza di italiano ed inglese e capacità di schematizzare processi/documenti
- Preferibile la conoscenza dei sistemi TrackWise e Documentum
- Preferibile conoscenza, anche di base, in ambito regolatorio (scrittura specifiche)
