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51235MKP - Bioassay Quality Control Analyst (LeanBioPro)


  • Ubicació: Barcelona (Espanya)
  • Tipus de Contracte: Indefinit
  • Jornada: Jornada completa
  • Sector: Farmacèutica i biofarmacèutica
  • Vacants: 1
  • Salari: 36000/46000€ Brut/any
  • Disciplina: Innovation
  • Modalitat de treball: Presencial

Barcelona Activa

BARCELONA 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. 

 

Descripció de l'oferta

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:  Bioassay Quality Control Analyst

Only those who meet the company's requirements will be notified.

Attendance and details will be confirmed by email.

 

ABOUT BIOPRO

  • 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 cell proliferation methods and others bioassays to verify the potency of biotechnology products, according to to USP, EP, and internal methodologies. Cell bank production, caracterization and release management. Maintain detailed and contemporaneous records in laboratory notebooks, logbooks, or electronic systems (LIMS). 

Participate in quality system activities including investigation of OOS/OOT microbiological results, deviation reporting, and support in CAPA implementation. Maintain laboratory equipment calibration and functionality and promptly report any malfunctions or maintenance needs. Follow all biosafety and safety protocols contributing to maintaining a clean, organized, and compliant laboratory environment. Collaborate effectively with QA, production, validation, and other cross-functional teams to support quality assurance and compliance.

 

OFFERED

  • Type of professional relationship: Contract
  • Type of contract: Permanent
  • Hours per 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.

Requisits

REQUIREMENTS

  • Advanced training in bioassays analysis with 2 to 5 years of proven experience in Quality Control within a GMP-regulated pharmaceutical environment.
  • Practical expertise in bioassays used in biotechnology, including cell proliferation assay, following USP and EP methods. Skilled in cell culture.
  • Strong knowledge of ALCOA++ data integrity principles and GMP documentation practices.
  • Experienced in managing quality systems including Out of Specification (OOS) investigations, deviation reporting, CAPA implementation, and change control.
  • Proactive team player with strong organizational skills and the ability to work independently while ensuring strict compliance with regulatory requirements. Fluent in Spanish with basic to intermediate English communication skills (reading and writing preferred).
  • Categoria professional: Tècnics superiors i assimilats
  • Education:  reglada requerida: m. Doctorat - m. Doctorat, o. Master Oficial (Bolonia) - o. Master Oficial (Bolonia)

  • Ubicació: Barcelona (Espanya)
  • Tipus de Contracte: Indefinit
  • Jornada: Jornada completa
  • Sector: Farmacèutica i biofarmacèutica
  • Vacants: 1
  • Salari: 36000/46000€ Brut/any
  • Disciplina: Innovation
  • Modalitat de treball: Presencial