Validation Technician

COMSER; Sevilla; Presencial; EUR 10.000 - 30.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical services company in Sevilla is seeking a Qualification and Validation Technician. This entry-level position will involve designing validation protocols and executing them in compliance with GMP standards. Ideal candidates will have a scientific background and proficiency in English. A vibrant work environment with opportunities for career growth is offered.

Servicios

Career development opportunities

Multidisciplinary team participation

Positive work environment

Formación

• Knowledge of GMP regulations and aseptic manufacturing is a plus.
• Proficiency in English (spoken and written).
• Own vehicle required for client site visits.

Responsabilidades

• Design equipment or process validation protocols according to GMP.
• Execute and review protocols, analyzing results.
• Continuously improve validation documentation and standards.

Conocimientos

Analytical skills

Organizational skills

Results-oriented

Dynamic individual

Educación

Scientific-technical university degree

Descripción del empleo

2 days ago, be among the first 25 applicants.Direct message the job poster from COMSER.HR & Finance Manager / / Management, People & Values / / CCA Certificate / / Executive MBACOMSER is seeking a Qualification and Validation Technician for the GMP Compliance Services area. We are a company providing services to the pharmaceutical industry.Our mission is to facilitate and streamline the industrialization of new medicines that enhance people's quality of life. We focus on injectable medicines manufactured in aseptic environments.What do we offer?Career development with personalized professional growth in the pharmaceutical sector within a growing company with numerous opportunities.Participation in a multidisciplinary team, where scientific and engineering profiles are prominent, and your creative proposals are valued.Acting as the direct contact with clients during project execution.A positive and youthful work environment.What will your main responsibilities be?Designing and developing equipment or process validation protocols in accordance with GMP and the client's user requirements.Executing and reviewing protocols, analyzing results.Continuously improving validation documentation and updating standards to suit each project.What do we expect from you?You should have a scientific-technical university degree (chemical sciences, pharmacy, biology, chemical engineering, or similar) and / or relevant professional training.You are an analytical, organized, resolute, results-oriented, and dynamic individual.Knowledge of GMP regulations, aseptic manufacturing, and lyophilization techniques is a plus.Availability to travel (domestically and internationally).Proficiency in English (spoken and written).Own vehicle required for client site visits.At COMSER, we value and respect diversity. We believe that having a diverse team is key to success and innovation. We offer equal opportunities to all candidates, regardless of gender, age, race, religion, sexual orientation, disability, or other characteristics.If you believe you are a good fit and are interested in starting a new professional journey, please apply and contact us. We look forward to meeting you!Seniority levelEntry levelEmployment typeFull-timeJob functionManagement and ManufacturingPharmaceutical ManufacturingJ-18808-Ljbffr

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