Quality Control Technician VHIOs clean room

VHIR; Barcelona; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A leading research institution in Barcelona is seeking a qualified professional for quality control of Advanced Therapies Medicinal Products (ATMPs). The role involves performing analytical and microbiological tests, ensuring compliance with GMP standards, and managing inventory. Ideal candidates possess a scientific background with experience in cellular techniques and quality assurance in a laboratory setting. This full-time position offers competitive remuneration and a dynamic working environment.

Servicios

Flexible working hours

23 days of holidays

Health insurance

International mobility support

Formación

• Fluency in Catalan, Spanish, and English is essential.
• Knowledge of GMP and quality guidelines specific for ATMPs is a plus.
• Experience in T-cell based ATMP is desired.

Responsabilidades

• Conduct analytical and microbiological tests on raw materials.
• Ensure compliance with specifications through analytical method validation.
• Manage inventory control of raw materials and finished products.

Conocimientos

Technical and practical knowledge of molecular biology

Experience in cell culture techniques

Fluency in Catalan

Fluency in Spanish

Fluency in English

Educación

Higher Vocational Training Diploma / University Degree / Master in scientific or healthcare fields

Herramientas

Computer skills (Office suite)

Descripción del empleo

Reporting to the Clean Room - Advanced Therapies Medicinal Products (ATMPs) Qualified Person (QP) and the Manufacturing Manager of VHIO the mission of the role will be to ensure at all ATMPs meet the required quality safety and efficacy standards before being released.

Education and Qualifications

• Higher Vocational Training Diploma University Degree Master or equivalent qualification in the scientific or healthcare field.
• Fluency in Catalan Spanish English

Experience and Knowledge

Required:

• Technical and practical knowledge of molecular biology immunology and microbiological techniques (qPCR flow cytometry ELISA mycoplasma endotoxin etc.).
• Experience in cell culture techniques.
• Experience working in quality control laboratories cell culture laboratories or controlled conditions (clean rooms or similar environments).
• Experience with drafting technical documents and protocols. Experience with laboratory equipment.
• Computer skills (Office suite and Internet).

Desired:

• Knowledge of GMP and quality guidelines specific for ATMPs.
• Experience in analytical method validation for the release of clinical-grade ATMPs.
• Experience in T-cell based ATMP such as TIL PBL CAR-T and TCR.
• Technical and practical knowledge of tissue manipulation biotechnological techniques and viral vector handling in controlled conditions (clean rooms or similar environments).
• Experience in aseptic processes as well as aseptic process validations.
• Experience in process development for GMP manufacturing.

Main Responsibilities and Duties

• Performing analytical and microbiological tests on raw materials in-process samples and intermediate and final products to verify compliance with specifications.
• Performing analytical method validation in accordance with GMP standards.
• Manage the inventory control of raw materials starting materials intermediates and finished pharmaceutical products.
• Reviewing and validating test results and documentation of analytical testing to ensure data integrity and regulatory compliance.
• Ensuring proper documentation and traceability of all QC activities as part of the batch release process.
• Documenting each step of the process meticulously to maintain traceability and compliance.
• Preparing and operating equipment in accordance with strict protocols. Participate in the verification / calibration of analytical instruments. Ensure the proper use and maintenance of laboratory equipment in accordance with GMP standards.
• Contributing to the drafting and revision of standard operating procedures (SOPs) always ensuring their implementation and full compliance with GMP regulations.
• Supporting quality assurance activities such as in-process controls and deviation reporting.
• Identifying and reporting deviations or non-conformities and collaborating with other departments in root cause investigations.
• Supporting process validation in accordance with GMP standards.
• Supporting environmental monitoring of the cleanroom to ensure sterile conditions are maintained.
• Supporting handling and processing biological materials under sterile conditions.

Competences

• Flexible mindset
• Teamplayer
• Innovative
• Proactive

Labour Conditions

• Full‑time position
• Starting date: immediate
• Gross annual salary: Remuneration will depend on experience and skills. Salary ranges are consistent with our Collective Agreement pay scale.
• Contract: Technical and scientific activities contract linked to the project activities.

What We Offer

• Incorporation to Vall dHebron Research Institute (VHIR) a public sector institution that promotes and develops the biomedical research innovation and teaching at Vall dHebron University Hospital (HUVH) the biggest hospital of Barcelona and the largest of Catalan Institute of Health (ICS).
• A scientific environment of excellence highly dynamic where high-end biomedical projects are continuously developed.
• Continuous learning and a wide range of responsibilities within a stimulating work environment.
• Individual training opportunities.
• Flexible working hours.
• 23 days of holidays 9 personal days.
• Flexible Remuneration Program (including dining checks health insurance transportation and more)
• Corporate Benefits: platform through which you can obtain significant discounts on travel culture technology gastronomy sports ... among many others.
• Healthy Offering: choose from a variety of wellbeing focused activities to be the healthiest you.
• International Mobility Support (Welcome Services): We aim to make your arrival in Barcelona smooth and pleasant by providing city information guidance on required procedures access to the International Welcome Desk family recommendations and support in finding accommodation.

Hiring Process

1. Pre-selection: Candidates are shortlisted based on their skills, qualifications and relevant experience as outlined in their CVs.
2. Interviews: Meetings may be held with Talent Acquisition and/or the hiring manager.
3. Practical assessment: Depending on the role candidates may complete a case study, technical task, presentation or written exercise on‑site or remotely.
4. Checks: Education references and other job‑related verifications may be carried out.
5. Job offer: The selected candidate receives a formal job offer upon successful completion of the process.

VHIR embraces Equality and Diversity. As reflected in our values we work toward ensuring inclusion and equal opportunity in recruitment, hiring, training and management for all staff within the organization regardless of gender, civil status, family status, sexual orientation, gender identity and expression, religion, age, functional diversity or ethnicity.

Key Skills

• Quality Assurance
• Quality Inspection
• Calipers
• Coordinate Measuring Machine
• Food Industry
• GD&T
• ISO 9001
• Math
• Micrometer
• Quality Control
• HACCP
• Manufacturing

Employment Type: Full Time

Experience: years

Vacancy: 1