QA/QC Engineer Junior

Anotech; Schelle; On-site; EUR 38,000 - 48,000; Full time

Job summary

Anotech, a subsidiary of ALTEN, is seeking a Junior QA/QC Engineer to support quality teams across projects in the pharmaceutical industry. You will contribute to maintaining the Quality Management System and ensuring compliance with GMP/GxP requirements.

You will participate in deviations, CAPAs, change controls, audits, and continuous improvement initiatives, while working on the shop floor with cross-functional teams. English and Dutch proficiency are required.

Qualifications

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

Communication skills

Dutch language

English language

French language (advantage)

Education

Master's degree in Pharmacy, Industrial Pharmacy, Chemistry, Biology 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

A subsidiary of ALTEN, Anotech provides complementary expertise in project execution and operational engineering to optimize schedules, budgets, and quality. Specializing in high-CAPEX energy projects, we support major clients throughout the entire project lifecycle, from strategic planning to deployment. With a presence in more than 30 countries, including Houston, the Netherlands, Dubai, Singapore, and Shanghai, we support in operating effectively in complex, multicultural environments, delivering large-scale energy projects with efficiency and reliability.