QA/QC Engineer Junior

Anotech Energy company; Schelle; Remote; EUR 38,000 - 60,000; Full time

Job summary

Anotech Energy is expanding its pharmaceutical quality team and seeks a Junior QA/QC Engineer to support quality activities across projects. You will help maintain the Quality Management System and ensure GMP/GxP compliance on the shop floor, while collaborating with production and laboratory teams to uphold quality standards.

You will contribute to deviation handling, CAPAs, change controls, audits, and continuous improvement initiatives, gaining hands-on experience in a highly regulated

Qualifications

• Master's degree in Pharmacy, Industrial Pharmacy, Chemistry, Biology, or a related scientific field.
• First experience through internships, apprenticeships, or academic projects in a pharmaceutical environment is an asset.
• Good knowledge of GMP/GxP requirements.
• Fluent in Dutch with a good command of English; knowledge of French is considered an advantage.

Responsibilities

• Participate in quality documentation management (procedures, work instructions, reports, and records)
• Support the handling of deviations, CAPAs, and change controls
• Assist in monitoring quality control activities
• Contribute to quality investigations and root cause analyses
• Review production and laboratory documentation to ensure compliance
• Support internal and external audits
• Participate in continuous improvement initiatives within the Quality Management System
• Ensure GMP/GxP requirements are applied and maintained on the shop floor

Skills

Analytical skills

Attention to detail

Organizational skills

Team player

Communication skills

Dutch language

English language

French (advantage)

Education

Master's degree in Pharmacy or related field

Job description

As part of the growth of our activities within the pharmaceutical industry, we are looking for a Junior QA/QC Engineer to support quality teams across various projects.

You will contribute to maintaining and continuously improving the Quality Management System while ensuring compliance with GMP requirements and applicable regulatory standards.

Responsibilities

• Participate in quality documentation management (procedures, work instructions, reports, and records)
• Support the handling of deviations, CAPAs, and change controls
• Assist in monitoring quality control activities
• Contribute to quality investigations and root cause analyses
• Review production and laboratory documentation to ensure compliance
• Support internal and external audits
• Participate in continuous improvement initiatives within the Quality Management System
• Ensure GMP/GxP requirements are applied and maintained on the shop floor
• Master's degree in Pharmacy, Industrial Pharmacy, Chemistry, Biology, or a related scientific field
• First experience through internships, apprenticeships, or academic projects in a pharmaceutical environment is an asset
• Good knowledge of GMP/GxP requirements
• Strong analytical skills, attention to detail, and organizational abilities
• Team-oriented with good communication skills
• Fluent in Dutch with a good command of English
• Knowledge of French is considered an advantage

Nice to Have

• Understanding of pharmaceutical quality systems
• Interest in highly regulated environments
• Motivation to develop a career in QA/QC and take on increasing responsibilities over time