The English-language job board for Spain

Quality Control Technician

On-site in Paterna·Full-time·Added yesterday (last checked 20 Oct)

Curapath

3 open roles

Overview

Work mode
On-site, Paterna
Contract
Fixed-term contract, full-time hours
English
Required
Experience
2+ years
Education
University degree

Visa options

  • The ad doesn’t mention sponsorship

    Not a refusal, but not a yes. Worth asking in your first message.

Find jobs with visa support

Skills

This job advert was originally written in Spanish.

Requirements

What we're looking for

  • Degree in Chemistry, Pharmaceutical Sciences, Biotechnology, or similar.

  • At least 2 years of professional experience.

  • Intermediate English, spoken and written.

Pay & benefits

What you'll get

  • Temporary contract for substitution.

  • Position with a high level of learning and continuous improvement.

  • Very good working environment.

  • Flexible hours.

The role

Curapath is a full-service CDMO (Contract Developing and Manufacturing Organizations) that connects innovative technology and scientific precision, centralizing your manufacturing process from preclinical to clinical development. We offer the best drug delivery solutions to potential clients seeking specific therapies.

We believe in science to transform the world, and we want the people who work at Curapath to thrive in an environment that makes this possible. That is why we are committed to developing the talent of every person in our company.

What you'll do

  • Understand, use, and execute the SOPs and instructions provided, including sampling and analysis of raw materials, stability studies, IPC, release, R&D samples, standards, and cleaning verifications.

  • Perform routine laboratory work such as mobile phase preparation, equipment conditioning, preparation of standards and samples, measurements, stock controls, and basic equipment maintenance.

  • Perform basic handling of analytical equipment such as chromatography, IR, Karl Fischer, pH/conductivity, and osmolality.

  • Prepare samples, execute SOPs, and perform basic calculations and data analysis under guidance.

  • Draft the investigation part of deviations, change controls, CAPAs, and OOS under supervision.

  • Prepare certificates of analysis (CoAs) in accordance with established specifications.

  • Draft SOPs, analytical methods, TIs, general procedures, protocols, and reports following existing templates, as well as maintaining the laboratory notebook.

  • Use and understand relevant technical bibliography.

  • Routinely control standards, reagents, and product/solution stocks, ensuring their proper labeling, storage, and traceability.

  • Participate in the general cleaning of the workplace and in maintaining laboratory order, complying with established good practices.

About Curapath

Curapath is a biotech Contract Development and Manufacturing Organization (CDMO) based in Barcelona, Spain, specializing in the development and production of advanced therapies, including cell and gene therapies. The company provides end-to-end services from process development to clinical and commercial manufacturing, supporting biotech and pharmaceutical clients in bringing innovative treatments to market. As a CDMO, Curapath operates at the intersection of biotechnology and manufacturing, with a focus on quality, regulatory compliance, and scalability.

Curapath's operations are centered in Barcelona, a key European biotech hub, and the company is actively expanding its team to support growing client demand. The work culture emphasizes scientific excellence, innovation, and collaboration, making it an attractive destination for international professionals with expertise in bioprocessing, quality assurance, and regulatory affairs. With a small but growing team, Curapath offers the opportunity to have a significant impact in a fast-paced, mission-driven environment.

Industry
Biotech CDMO
Employees
50
Headquarters
Barcelona, Spain
In Spain
Barcelona

Good to know if you are moving

  • Curapath is based in Barcelona, a leading European biotech hub with a strong international community and excellent quality of life.
  • As a CDMO, Curapath offers roles in bioprocessing, quality, and manufacturing, which are in high demand globally, providing valuable experience for career growth.
  • The company is small and growing, which may offer greater visibility and faster career progression compared to larger organizations.
  • Working at Curapath involves collaboration with international clients, making English a likely working language alongside Spanish.
  • Spain offers a favorable work-life balance and a relatively lower cost of living compared to other European biotech hubs.

In their own words

About the company & team

At Curapath, we are looking for a Quality Control Technician to join our team. The selected person will execute the necessary actions to ensure the satisfactory completion of the assigned project, guaranteeing overall alignment with Curapath's objectives.

All open roles at Curapath
WhatsApp
Hybrid in PaternaNo Spanish needed

Work with us

Curapath2w ago
Paterna
See all 3 jobs