Quality Assurance Technician - Process Validation
At Medinfar, your work has a real impact: helping to bring healthcare to everyone. Join a team driven by purpose, innovation, ethics, and sustainability.
👉 Together, we care better.
Your role at Medinfar As a Quality Assurance Technician - Process Validation, you will be responsible for generating documentary evidence that demonstrates that manufacturing processes are robust, consistent, and capable of producing reproducible results, ensuring the maintenance of the validated state throughout their entire life cycle. How will you make a difference? Attention to detail: Prepare, review, and execute process validation protocols and reports, ensuring the robustness and reliability of manufacturing processes.
Regulatory knowledge: Ensure that validation activities comply with GMP requirements, SOPs, and other applicable standards.
Analytical capacity: Evaluate manufacturing data and analytical results of processes and support technical decisions based on evidence.
Process validation throughout the life cycle: Participate in the introduction of new products through the execution of process validation activities and ensure continuous monitoring and periodic revalidations necessary to maintain the validated state of the processes.
Multidisciplinary collaboration: Work in close collaboration with R&D, Production, Quality Control, Quality Assurance, and other technical areas to ensure project success and compliance with respective deadlines.
Documentary organization: Ensure the timely preparation, review, and availability of validation documentation, ensuring compliance with project deadlines and manufacturing activities.
Problem solving: Actively participate in the opening and investigation of deviations and in the implementation of corrective and preventive actions that ensure the maintenance of the validated state.
What we are looking for: Master's degree in Pharmaceutical Sciences, Chemical Engineering, Biological Engineering, Biotechnology, Chemistry, or a similar field.
Attention to detail, strong critical thinking, and analytical capacity to interpret results, solve problems, support technical decisions, and identify improvement opportunities.
Experience in a GMP environment in the pharmaceutical industry, preferably in the area of Manufacturing Process Validation and Production.
Knowledge of GMP and regulatory requirements applicable to the pharmaceutical industry.
Good computer skills in Microsoft Office.
Intermediate or advanced level of English (mandatory).
Good communication and teamwork skills.
Excellent organizational capacity and results orientation.
Why Medinfar? Because here you will find more than a professional challenge. You will find purpose, impact, growth, and a team that believes that, when we care for one another, we care better for everyone.
Help us build a better future for all. 👉 Together, we care better.