Recipharm is hiring a Technician for the Computer System Validation (CSV) + Commissioning & Qualification (C&Q) area!
Recipharm is a leading pharmaceutical company with over 75 years of experience providing integrated services, from drug development to manufacturing, always ensuring high standards of quality, safety, and regulatory compliance.
To strengthen our Engineering Department, we are looking for a Technician for the Computer System Validation (CSV) + Commissioning & Qualification (C&Q).
The core mission is to manage the day-to-day execution of validation activities. Your mission is to perform the tests, verifications, and document every step to ensure our systems remain in a state of compliance.
This role bridges quality assurance, engineering, and IT to ensure data integrity and process safety.
Key responsibilities
- Protocol Management: Author and approver of critical validation deliverables, including Validation Master Plans (VMP), Risk Assessments, and IQ/OQ/PQ protocols.
- Protocol Execution: Perform physical testing for Installation (IQ), Operational (OQ), and Performance Qualification (PQ)on new and existing equipment.
- System Verification: Verify that equipment is correctly connected to utilities and that all software and firmware versionsmatch the approved specifications.
- Operational Checks: Conduct functionality tests, including checking alarms, fail-safes, and control systemsto ensure equipment operates within safe limits.
- Documentation & Record-Keeping: Meticulously record test results, troubleshoot deviationsduring execution, and maintain clean, organized validation files according to GxP standards.
- Continuous Improvement: Drive the transition toward "digital validation" and paperless systems while maintaining a high state of inspection readiness.
Profile
- Education: Master degree in Engineering, Life Sciences, Computer Science, or a related technical field.
- Experience: 1-3+ years in a highly regulated GxP environment (Pharma/MedTech), with proven experience in both hardware qualification and software validation.
- Technical Expertise: Deep knowledge of GAMP 5, Risk-Based Validation, and the V-Model. Familiarity with systems like LIMS, PLC, or MES is a major plus.
- Soft Skills: Excellent technical writing skills and the ability to explain complex compliance requirements to non-technical stakeholders.
- • Solid knowledge of GMP and Good Engineering Practices (GEP);
- • Good IT skills and fluency in English;
What we offer
- Integration into a solid and growing international company;
• Integration into a specialized technical team focused on innovation and continuous improvement;
• Salary package aligned with the role and experience.
Location: Lisbon
Schedule: Full-time
If you are looking for a leadership challenge in a critical area for the quality and safety of medicines, we encourage you to apply.