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(Job Opening) - Medinfar

Indeed

Company

Job typeFull-time
Workplace typeOnsite
Experience levelNo experience limit
Education levelNo degree limit

Description

Job Summary: The Quality Assurance Supervisor \\ Process Validation at Medinfar will be responsible for developing, implementing, and managing process validation activities, ensuring regulatory compliance and continuous improvement. Key Highlights: 1. Team driven by purpose, innovation, ethics, and sustainability. 2. Real impact: helping deliver healthcare to everyone. 3. Professional growth and career development. At Medinfar, your work makes a real impact: helping deliver healthcare to everyone. Join a team driven by purpose, innovation, ethics, and sustainability. **Together, we care better.** **Your role at Medinfar** As the ***Quality Assurance Supervisor*** **\\ Process Validation**, you will be responsible for developing, implementing, and managing validation activities, ensuring manufacturing processes meet regulatory requirements and promoting continuous improvement in line with industry standards at our industrial facility in Condeixa, Coimbra. **How will you make a difference?** * **Attention to detail:** Develop, review, and execute validation protocols/reports for manufacturing processes. * **Regulatory knowledge:** Ensure all validation activities comply with GMP, SOPs, and other regulatory requirements. * **Analytical ability:** Conduct risk assessments and develop validation strategies. * **Project management:** Collaborate with other teams to ensure validation activities are integrated into project timelines. * **Document management:** Maintain and update validation documentation, including master plans, protocols, and reports. * **Problem solving:** Investigate and resolve deviations and occurrences related to validation. * **Professional development:** Stay informed about industry trends and regulatory changes to ensure ongoing compliance. **What we are looking for:** * Minimum 3 years of experience in the pharmaceutical industry, preferably in Manufacturing Process Validation or Production. * Master’s degree in Pharmaceutical Sciences, Chemical Engineering, or a related field. * Proficiency in Microsoft Office (Excel). * Excellent command of English (mandatory). * Strong critical thinking, problem-solving, and decision-making skills. * Good teamwork and proactive attitude; * Strong organizational, prioritization, planning, and results-oriented skills. **Why Medinfar?** Because here you’ll find more than just a professional challenge. You’ll find purpose, impact, growth, and a team that believes that when we care for each other, we care better for everyone. **Help us build a better future for all.** **Together, we care better.**

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Posted by

João Santos

Indeed · HR

Location

João Santos

Indeed · HR

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