About this role TFS HealthScience is a leading global
mid-size Contract Research Organization (CRO) that partners with
biotechnology and pharmaceutical companies across development and
manufacturing. Our expertise includes full-service capabilities,
resourcing, and Functional Service (FSP) solutions. The Quality
Systems Specialist (GMP) is responsible for supporting and
maintaining quality systems within a GMP-regulated pharmaceutical
manufacturing environment. This includes ensuring compliance
through audit activities, CAPA management, and effective quality
system processes. As part of our SRS/FSP team, you will be
dedicated to one sponsor, a integral pharmaceutical company operating
within a GMP-regulated manufacturing environment. Contract: 3-month
consultancy Key Responsibilities Support and maintain Quality
Management System (QMS) activities in line with GMP requirements
Manage and follow up on CAPAs, ensuring timely closure and
effectiveness Perform and support internal and supplier audits
Support supplier qualification and ongoing supplier management
activities Maintain GMP documentation, including document control
and training records Participate in change control processes and
ensure compliance with internal procedures Support GMP training
management activities Collaborate with cross-functional teams to
ensure quality and compliance standards Qualifications Bachelor’s
degree in Life Sciences or a related field Minimum 3 years of




experience within Quality Assurance in a GMP environment Strong
knowledge of GMP regulations and quality systems Experience with
CAPA management and audit activities (internal and/or supplier
audits) Experience with document control, change control, and
training management Experience within pharmaceutical manufacturing
(injectables or sterile environment is a plus) Strong communication
skills in English (written and spoken) Ability to work
independently and manage multiple priorities What We Offer We
provide opportunities for personal and professional growth in a
rewarding environment. You will join a team that values
collaboration, quality, and making a difference in the lives of
patients. Our core values of Trust, Quality, Passion, Flexibility,
and Sustainability guide our decisions and shape our culture. By
aligning on these values, we foster collaboration, innovation, and
a shared commitment to excellence. Together, we make a difference.
A Bit More About Us Our journey began over 30 years ago in Sweden,
in the city of Lund. As a full-service global CRO, we build
solution-driven teams working toward a healthier future. Bringing
together over 600 professionals, TFS delivers tailored clinical
research and resourcing services in more than 50 countries,
supporting both clinical development and GMP-regulated
manufacturing environments across key therapeutic areas including
Dermatology, Neuroscience, Oncology, and
Ophthalmology.

📌 Quality Systems Specialist (GMP) (Madrid)
🏢 TFS HealthScience
📍 Madrid