60559MKP - Scientist for Biologics Quality Control (morning shift) (KYMOS)

Ubicació: Barcelona (Espanya)
Tipus de Contracte: Indefinit
Jornada: Temps parcial
Sector: Farmacèutica i biofarmacèutica
Vacants: 1
Salari: 27000/39000€ Brut/any
Disciplina: Altres
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 job posting is part of the Talent Biohealth Job Marketplace, which will take place in person at CONNECTION DAY'26 on May 6 from 3:00 PM to 6:00 PM. The event is organized by Barcelona Activa in collaboration with Clúster Catalonia.Health at the World Trade Center building.

KYMOS is seeking to fill 1 position for the following role: .

Only candidates who meet the company’s requirements will be contacted. Attendance and details will be confirmed via email.

ROLES and RESPONSABILITIES

We are seeking a highly motivated Scientist to join our Biologics and Advanced Therapies Quality Control team. This role, reporting to the Department Manager, focuses on the analysis of biological products in a GMP-regulated environment.

Key responsibilities:

Design, execution, and oversee of analytical method development and validation studies for biologic products, including monoclonal antibodies, recombinant proteins, and advanced therapies.
Hands-on experience with techniques such as HPLC, capillary electrophoresis, ELISA, protein quantification (e.g., BCA, UV), and other relevant biochemical methods.
Lead and manage assigned development and validation projects, ensuring timely execution, compliance with regulatory requirements, and effective communication with internal and external stakeholders.
Draft, review, and manage technical documentation including method validation protocols and reports, SOPs, risk assessments, and technical justifications.
Collaborate with cross-functional teams including Quality Assurance and Marketing to support method development and validation.
Supervise and mentor laboratory analysts and technical staff during experimental work, promoting scientific excellence and GMP compliance.

OFFER

Contract type: Permanent

Hours per week: 20

Working hours: 2pm to 10pm

Gross annual salary: €27,000–€39,000 if it were a full-time job

Requisits

Requirements:

Bachelor's or higher degree in Biochemistry, Biotechnology, Pharmacy, or a related life science field.
Solid hands-on experience in analytical method development and validation for biologics, particularly using HPLC, capillary electrophoresis, and immunoassay-based techniques.
In-depth understanding of GMP requirements and ICH guidelines relevant to analytical method validation.
Experience with HPLC and Capillary electrophoresis development will be considered a strong asset.
Excellent organizational and documentation skills, with the ability to manage multiple projects simultaneously.
English level equivalent to Cambridge First Certificate (B2) or higher.
Willingness and availability to work the afternoon shift (2:00 PM – 10:00 PM).

Ubicació: Barcelona (Espanya)
Tipus de Contracte: Indefinit
Jornada: Temps parcial
Sector: Farmacèutica i biofarmacèutica
Vacants: 1
Salari: 27000/39000€ Brut/any
Disciplina: Altres
Modalitat de treball: Presencial

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