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Technical responsible - quality assurance (veterinary medicines)

Antas (Provincia de Pontevedra)
MNDP INNOVA
Medicina
Publicada el 31 marzo
Descripción

We are a fast-growing Animal Health MAH with a strong R&D and technological development backbone. Innovation is at the core of our value proposition, and we work closely with multiple stakeholders to bring solutions to life. Our way of working is agile and "startup-like": hands-on, collaborative and focused on execution with rigor. As we scale, we are building a solid team of people who take ownership, enjoy learning, and want to grow with the company while making a real impact.


La información a continuación detalla los requisitos del puesto, la experiencia esperada del candidato y las cualificaciones correspondientes.

The mission

You will help us "do Quality properly" while we keep moving fast. Your main focus will be to build, implement and run our Quality Management System, ensuring compliance and continuous improvement. You will work closely with R&D, Regulatory and other teams, and support coordination with AEMPS within the Technical Responsible scope (as required).

What you'll do (Responsibilities)

• Build and scale the QMS: design, implement and continuously improve a fit-for-purpose Quality Management System aligned with company's growth (SOPs, templates, logs, training and records).

• Own document control end-to-end: manage the full document lifecycle (drafting, review, approval, versioning, distribution and archiving).

• Make GDP operational: translate GDP requirements into practical workflows (distribution flows, storage/transport controls and third-party oversight) that teams can follow day-to-day.

• Run core QA processes: deviations/non-conformances, CAPAs, risk-based change control, training/competence records, supplier qualification/monitoring (as applicable), and quality metrics/continuous improvement.

• Audit readiness: prepare documentation packs, support internal/external audits and inspections, and drive follow-up actions to closure with evidence and effectiveness checks.

• Cross-functional integration: partner with R&D and Regulatory to embed quality requirements into operations and development activities (documentation readiness, traceability, training, controlled processes).

• Authority interface support (AEMPS): support coordination and compliance-related interactions/documentation within the Technical Responsible scope (as required).

• Support beyond QA when needed (secondary): contribute to light coordination of pharmacovigilance interfaces and/or regulatory documentation readiness, depending on business needs.

What we're looking for

• Pharmacy degree (Pharmacist) — mandatory.

• 2+ years of experience in Quality Assurance in regulated environments (ideally veterinary medicines / pharma / healthcare).

• Practical understanding and exposure to GDP (implementation experience is a plus).

• Comfortable building structure from scratch and improving it iteratively in a growing environment.

• Strong documentation discipline and stakeholder management skills.

• English is mandatory (professional level). Spanish is highly desirable.

• Based in Galicia is ideal; otherwise remote with occasional travel.

Mindset that will make you successful

• Ownership and accountability: you take responsibility and close loops.

• Execution focus: you turn requirements into practical ways of working.

• Learning agility and adaptability: you enjoy growing with the business.

• Cross-functional attitude: you like working with R&D/Regulatory and other team

What we offer

• A real build-and-own role: you won't be "maintaining someone else's system"—you'll help shape the way Quality is done at our company.

• High impact, fast learning: strong exposure to R&D, technology development and cross-functional stakeholders. You'll see the impact of your work quickly.

• Remote-first with flexibility: ideally based in Galicia, but remote is fine—with occasional travel when it really adds value (workshops, audits, key alignment moments).

• A pragmatic culture: we care about compliance and doing things right, but we avoid unnecessary bureaucracy. We value clarity, ownership and execution.

• Growth journey: a company in a strong growth phase where you can grow with it—responsibility increases as the business scales.

• Salary aligned to profile and experience (indicative around €30k, within budget parameters), plus the opportunity to take real ownership.

Interested? xsgfvud

If you want to grow your career in Quality Assurance within an Animal Health environment where you learn fast and see the impact of your work every day, we'd love to hear from you.

Please send us your CV and a brief cover note with the subject line REF2026155 to, and tell us why you're a great match for our company and this role.

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Inicio > Empleo > Empleo Salud > Empleo Medicina > Empleo Medicina en Antas (Provincia de Pontevedra) > Technical Responsible - Quality Assurance (Veterinary Medicines)

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