QA Specialist Jobs at Neuraxpharm, Spain | Life Sciences | Apply Now
Are you ready to transition your scientific expertise into a purpose-driven role that directly improves patients’ lives? Neuraxpharm, a European leader in central nervous system (CNS) therapies, is expanding its quality division. For professionals seeking high-impact QA Specialist Jobs, this Junior Quality Assurance Specialist position in Sant Joan DespÃ, Barcelona, offers an exceptional career milestone. Stepping into this temporary contract provides an immersive opportunity to master European compliance standards. It is a highly competitive Life Sciences Job designed for an ambitious professional looking to solidify their expertise as a world-class Quality Assurance Specialist.
About the Company
Neuraxpharm is a leading European specialty pharmaceutical company focused on the treatment of psychiatric and neurological disorders. With a unique understanding of the CNS market built over 40 years, the company constantly innovates to address unmet patient needs across more than 50 countries globally. Backed by funds advised by Permira, Neuraxpharm features a direct presence in over 20 European nations, alongside operations in Latin America, the Middle East, and Australia. Much of the core pharmaceutical manufacturing takes place at Neuraxpharm Pharmaceuticals (formerly Laboratorios Lesvi) in Spain, creating a dynamic, high-volume environment for quality professionals. The organization thrives on an inclusive culture that promotes diversity, result-focused performance, and individualized professional development within an ambitious international growth strategy.
QA Specialist Jobs – Key Responsibilities
The primary mission of a Quality Assurance Specialist at Neuraxpharm is to provide absolute confidence that quality requirements are fulfilled. You will ensure strict compliance with Good Manufacturing Practice (GMP) standards so that CNS products are consistently produced and controlled to marketing authorization specifications.
Your major accountabilities will include:
- Technical Documentation: Writing, reviewing, and approving critical technical documents, including Standard Operating Procedures (SOPs), master and batch manufacturing records, analytical methods, material lists, Out of Specification (OOS) reports, and stability studies.
- Qualification & Validation: Writing, executing, and reviewing qualifications for equipment, utilities, and facilities, alongside validations for manufacturing processes, cleaning procedures, IT systems, and storage/distribution networks.
- QMS Tracking & Monitoring: Writing and monitoring Corrective and Preventive Actions (CAPAs), deviations, and change controls, while actively supporting the maintenance of the overarching Quality Management System (QMS).
- Audits & Training: Preparing and executing internal and external audits, compiling Product Quality Review (PQR) reports, and delivering essential GMP training sessions to internal teams.
- Supplier Management: Participating in the technical management of suppliers and third-party services, ensuring external partners align with Neuraxpharm’s high quality standards.
Candidate Profile Required For QA Specialist Jobs
To stand out in the landscape of QA Specialist Jobs, candidates must bridge the gap between rigorous scientific theory and highly organized document control.
- Educational Foundation: A University Degree in Life Sciences (such as Biology) or Engineering is required to anchor your technical understanding of this Life Sciences Job.
- Targeted Experience: A minimum of 2 years of direct experience working within a pharmaceutical Quality Assurance Department.
- Regulatory & System Mastery: Demonstrated expertise in GMP guidelines and Quality Management Systems, with operational knowledge of specialized enterprise software including SAP, LIMS, and Veeva.
- Linguistic & Communication Skills: Fluency in English is a mandatory requirement, paired with strong interpersonal skills to coordinate with cross-functional, international teams.
- Core Capabilities: An analytical mindset, sharp problem-solving skills, exceptional attention to detail, and a natural orientation toward quality and continuous improvement.
Logistics, Working Conditions & Benefits
- Location: Sant Joan DespÃ, Barcelona, Spain (Fully on-site at the manufacturing facility).
- Contract Type: Temporary contract (Ideal for building immediate depth on your resume with complex European dossiers).
- Mobility: Availability to travel occasionally to conduct external audits and attend advanced professional courses.
- Compensation Package: Offers an attractive remuneration structure aligned directly with the experience and skills you bring to the table.
In summary, this Junior Quality Assurance Specialist role is far more than a standard corporate position—it is an invitation to protect the integrity of therapies that millions of CNS patients rely on daily. By securing this premier Life Sciences Job, you gain direct exposure to complex validation activities, global audits, and advanced documentation workflows. If you possess the required 2 years of QA experience and a meticulous commitment to GMP compliance, apply today to claim your spot in one of Barcelona’s top-tier QA Specialist Jobs.
