Validation Technician | Pharma (Hybrid)

We are looking for a "Validation Technician" to join a leading company in the pharmaceutical and equipment manufacturing sector, participating in qualification and validation projects for equipment and facilities under GMP regulations.

The selected person will be responsible for ensuring compliance with pharmaceutical quality standards and customer requirements, participating in all phases of project validation and qualification.

TASKS AND RESPONSIBILITIES 🚀:

• Ensure project quality through the correct execution of validation and qualification activities.
• Draft and execute qualification and validation documentation, including FDS/DQ, FAT, SAT, IQ and OQ.
• Coordinate quality assurance activities associated with assigned projects.
• Collaborate in the planning and monitoring of qualification activities.
• Collect, analyze, and agree on validation requirements with the client, ensuring compliance with internal and regulatory standards.
• Participate in the execution of Factory Acceptance Tests (FAT) together with the client.
• Execute SAT, IQ and OQ activities at the client's facilities.
• Drive continuous improvement of documentation and validation standards.
• Manage and supervise external qualifications, including protocol review and supplier monitoring.
• Provide support in the management and maintenance of documentation related to pharmaceutical regulations.
• Collaborate in the definition and monitoring of calibration plans for measuring instruments used during testing.
• Actively participate in continuous improvement initiatives for validation and quality processes.

REQUIREMENTS 🤹:

• 3 - 5 years of experience in validation and qualification activities within regulated environments.
• Knowledge of pharmaceutical regulations and applicable quality standards (GMP/GxP).
• Experience in drafting and executing DQ, FAT, SAT, IQ and OQ protocols.
• Ability to interpret and manage client requirements related to validations and qualifications.
• Skill to coordinate activities with multidisciplinary teams and clients.
• Good organizational, documentation, and project monitoring skills.
• Availability to travel to client facilities when necessary.
• Sufficient level of English to work with technical documentation and international clients.

OPTIONAL REQUIREMENTS:

• Previous experience in manufacturers of machinery or equipment for the pharmaceutical industry.
• Knowledge of instrument calibration and measurement systems.
• Experience managing external qualification and validation providers.
• Knowledge of sterilization processes, aseptic filling, or pharmaceutical equipment.
• Familiarity with audits, inspections, and highly regulated GMP environments.

SCHEDULE 🕘:

08/09h - 17/18h from Monday to Friday

1-2 days of remote work

CONDITIONS 🌱:

Permanent contract.

Flexible compensation program (medical insurance, public transport ticket, and childcare vouchers)

Discounts on the gym network (Urban Sport Club)

Training and development.

Friend referral program.

Our goal is for you to be well in every sense!