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Quality Assurance Specialist

On-site in Madrid·Added 25 days ago

Overview

Requirements

  • Have the right to work in Spain

    Project Delivery Partners doesn't mention sponsorship in the ad.

  • Speak fluent Spanish

    Listed as a requirement in the ad.

  • Work on-site in Madrid

    No relocation package mentioned.

  • Have 5+ years of experience

    Mid-level role.

Requirements

What we're looking for

  • Minimum 5+ years of experience in Quality Assurance (pharma, biotech, or related regulated fields).
  • Fluent in Spanish (spoken and written).
  • Solid experience with deviation investigations, CAPAs, change control.
  • Strong understanding of GMP, data integrity, validation processes, and quality systems.
  • Availability to work occasionally on weekends.
  • Excellent attention to detail, communication, and problem-solving skills.

The role

PharmEng / Efor is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative solutions to the challenges facing our industries. We pride ourselves on our dedication to quality, safety, and excellence in everything we do. As we continue to grow, we are looking for a highly qualified and motivated Automation Engineer to join our team.

We are looking for a highly skilled QA Specialist to join our Quality Assurance team. The ideal candidate brings strong GMP knowledge, experience in deviation/CAPA management, batch record review, and QA oversight in a regulated environment.

What you'll do

  • Perform QA oversight of daily operations, ensuring compliance with GMP and internal quality standards.
  • Review and approve deviations, CAPAs, change controls, and other quality records.
  • Support root cause investigations and ensure timely and effective CAPA implementation.
  • Conduct batch record review and release processes, ensuring data integrity and regulatory compliance.
  • Perform on-site GMP audits, walkthroughs, and quality checks on production and QC areas.
  • Support Environmental Monitoring (EM) oversight and ensure adherence to microbiological control strategies.
  • Participate in validation activities, such as equipment, utilities, and water system validation, from a QA perspective.
  • Ensure compliance with data integrity principles and maintain high-quality documentation.
  • Collaborate cross-functionally to promote continuous improvement and quality culture.

How you'll work

Language: Fluent Spanish
Availability: Must be available to work on weekends; minimum 6-month uninterrupted commitment

Position

Position: Quality Assurance Specialist

Experience Required

Experience Required: Minimum 5 years

About Project Delivery Partners

Project Delivery Partners (PDP) is a specialized consultancy providing project management, commissioning, qualification, and validation (CQV) services primarily for the life sciences and pharmaceutical industries. The company supports clients in the design, construction, and regulatory qualification of manufacturing facilities, ensuring compliance with Good Manufacturing Practices (GMP) and other industry standards. With a global footprint, PDP operates across multiple regions, including Europe, the US, and Asia, and is known for its expertise in delivering complex capital projects on time and within budget.

In Spain, PDP has a significant presence, with offices in Madrid and a strong focus on supporting pharmaceutical and biotech projects in the region. The company is actively hiring for a range of roles in Spain, including QA/QC specialists, validation experts, and project managers, many of which are remote or site-based. For international professionals, PDP offers opportunities to work on high-stakes projects in a growing life sciences hub, with a collaborative and dynamic work culture that values technical excellence and cross-border collaboration.

Founded
2005
Employees
500–1,000
Headquarters
London, UK
In Spain
Madrid

Good to know if you are moving

  • PDP offers remote and hybrid roles, which can facilitate relocation to Spain while working on international projects.
  • The company has a strong focus on life sciences, providing opportunities to work on cutting-edge pharmaceutical and biotech facilities.
  • PDP's global presence means employees may have opportunities to collaborate with teams across different countries.
  • The company values technical expertise and offers a dynamic work environment with a focus on professional development.

In their own words

Additional information

Join us: If you are a dedicated and highly motivated person with a passion for ensuring the highest standards of Quality Assurance in the Pharmaceutical Industry, we encourage you to apply. PharmEng / Efor offers a dynamic and inclusive work environment, competitive compensation, and opportunities for professional growth. Be part of our team and contribute to the success of our industry-leading solutions.

PharmEng/Efor is an equal opportunity employer and welcomes applicants from all backgrounds.

Thank you for your consideration and application! We review all resumes and submissions, however, due to the high volume of applications we receive, only approved candidates will be contacted.

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