Validation Technician

COMSER; Barcelona; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

COMSER is seeking a Qualification and Validation Technician to support GMP Compliance Services in the pharmaceutical industry. This entry-level role involves designing validation protocols, analyzing results, and improving documentation standards, with opportunities for career growth in a dynamic team environment.

Servicios

Career development opportunities

Positive and youthful work environment

Participation in a multidisciplinary team

Formación

• Degree in chemical sciences, pharmacy, biology, or similar required.
• Knowledge of GMP regulations and aseptic manufacturing is a plus.
• Proficiency in English (spoken and written) required.

Responsabilidades

• Design and develop validation protocols according to GMP.
• Execute and review protocols, analyze results.
• Continuously improve validation documentation.

Conocimientos

Analytical skills

Organizational skills

Results-oriented

Dynamic attitude

Educación

Scientific-technical university degree (chemical sciences, pharmacy, biology, chemical engineering, or similar)

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 MBA

COMSER 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 level

• Entry level

Employment type

• Full-time

Job function

• Management and Manufacturing
• Pharmaceutical Manufacturing

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