Ubicació: Barcelona (Espanya)
Tipus de Contracte: Indefinit
Jornada: Jornada completa
Sector: Farmacèutica i biofarmacèutica
Vacants: 1
Salari: 36000/46000€ Brut/anyDisciplina: Innovation
Modalitat de treball: PresencialBARCELONA ACTIVA gestiona ofertes d'empreses que necessiten cobrir vacants de personal. Les posicions que es publiquen no són per a Barcelona Activa. NOMÉS ES TINDRAN EN COMPTE LES CANDIDATURES QUE ARRIBIN PER AQUEST CANAL. El Servei de Cerca de Treballadors/es s'adreça a aquelles empreses del territori que necessiten incorporar nous professionals als seus equips i ofereix suport en la identificació de les vacants, el reclutament de personal i la preselecció de candidatures que s'ajustin als perfils sol·licitats.
This offer is part of the Job Marketplace of the Health Sector Talent event, which will take place in person at the Employment Fair on October 15th from 3:30 PM to 6:30 PM, organized by Barcelona Activa in collaboration with the Health Hub Barcelona.
LeanbioPro company needs to fill sales assistant vacances:Biochemical Quality Control Analyst
Only those who meet the company's requirements will be notified.
Attendance and details will be confirmed by email.
ABOUT LEANBIO
- Leanbio is a CDMO that develops and manufactures biopharmaceutical products as New biological entities and Biosimilars, located in Barcelona.
- Leanbio follows a knowledge-based strategy, applying cutting edge technological platforms and working altogether with customers.
- Leanbio is currently building a new GMP manufacturing facility with state-of-the-art technology that will cover all phases of the production process.
ROLE DESCRIPTION:
Perform routine and non-routine analyses of raw materials, intermediates, and finished products using biochemical techniques. Envolve in batch release, stability studies, comparability and molecular characterization.
Ensure strict adherence to GMP and ALCOA++ data integrity principles, maintaining complete, accurate, and traceable documentation.
Document all activities clearly and contemporaneously in lab notebooks, logbooks, or electronic systems (e.g., LIMS), in compliance with internal SOPs.
Participate in quality system activities, such as investigation of OOS / OOT results
reporting of deviations and support in CAPA implementation.
Maintain and calibrate laboratory equipment, performing routine checks and informing of any malfunction or need for maintenance.
Follow safety protocols and contribute to keeping the lab in a clean condition at all times.
Collaborate with cross-functional teams, including QA, production, and validation, when needed.
OFFERED
Type of professional relationship: Contract
Type of contract: Permanent
Hours week: 40 hours
Schedule: Intensive with flexible start times. Possibility of organizing shifts
Gross annual salary: 30k-45k depending on experience.
- Powerful professional development and growth contributing to the creation of the Quality Control department from scratch, and supporting GMP activities of the new manufacturing facility
- Be a part of a CDMO company that works with multiple biological products. You will have the opportunity to gain perspective of the life-cycle of a biological product.
REQUIREMENTS
Advanced Training in Laboratory Analysis and Control with 2–5 years of experience in Quality Control in a GMP-regulated pharmaceutical environment.
Practical experience in biochemical testing including HPLC, electrophoresis SDS-PAGE, capillary electrophoresis, ELISA, qPCR and UV-vis.
Skilled in verification and equipment calification following USP/EP methods.
Familiarity with environmental monitoring in cleanroom environments or physicochemicals methods will we a plus.
Strong knowledge of ALCOA++ principles and GMP documentation practices.
Experience with quality systems (OOS, deviations, CAPAs, change control).
Proactive team player with good organizational skills and the ability to work independently.
Fluent in Spanish with basic to intermediate English communication skills (reading/writing preferred).
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