GMP/GLP Quality Control Technician – Onsite Spain

Kenvue; Madrid; On-site; EUR 25,000 - 42,000; Full time

Benefits offered by this job

Competitive Benefit Package

Paid Holidays

Paid Vacation

Volunteer Time & More!

Extensive Learning & Development

Employee Resource Groups

Job summary

Kenvue is recruiting a Quality Control Technician to join our Europe/Middle East/Africa team onsite in Spain. You will ensure GLP and GMP compliance, execute analytical tests, and support documentation and data integrity across quality control activities.

The ideal candidate holds a science degree, has GMP knowledge, and communicates well in English. You will train staff, manage procedures, and contribute to CAPAs and quality system tasks in a collaborative lab environment.

Qualifications

• Bachelor-level or higher in a science field (Chemistry, Pharmacy or Biology).
• Proficient with GLP/GMP contexts and documentation.
• Good command of English and ability to work in a regulated lab.
• Experience with quality systems and statistical thinking.

Responsibilities

• Perform/review routine, stability, validation and transfer analytical tests following applicable procedures.
• Manage documentation, data integrity, and sample handling in the QC lab.
• Provide training to new staff and support ongoing training activities.
• Create/update QC procedures and instructions as needed.
• Contribute to Quality System activities (Investigations, GCCs, CAPAs).
• Collaborate in QC activities planning.

Skills

English (medium-high)

GMP knowledge

Problem-solving

Communication

Teamwork

Education

Science-related degree (Chemistry)

Science-related degree (Pharmacy)

Science-related degree (Biology)

Tools

Empower Software

Job description

Kenvue is recruiting a Quality Control Technician to join our Europe/Middle East/Africa team onsite in Spain. You will ensure GLP and GMP compliance, execute analytical tests, and support documentation and data integrity across quality control activities.

The ideal candidate holds a science degree, has GMP knowledge, and communicates well in English. You will train staff, manage procedures, and contribute to CAPAs and quality system tasks in a collaborative lab environment.