Quality Engineer II: Manufacturing Excellence

Planet Pharma Group; Kerkrade; On-site; EUR 55,000 - 75,000; Full time

Job summary

Planet Pharma is seeking a Quality Engineer II to strengthen manufacturing quality and ensure product integrity in a fast-paced, regulated environment. You will contribute to investigations, CAPA, data trend analysis, and cross-functional collaboration to drive continuous improvement.

In this role, you will support day-to-day manufacturing activities, maintain documentation, and uphold quality systems while communicating findings clearly to teams across QA, manufacturing, and compliance

Qualifications

• Bachelor’s degree with at least 4 years of relevant experience or advanced degree with 2 years of industry experience.
• Practical knowledge of quality systems, manufacturing processes, and documentation requirements.
• Proven ability to work independently on moderately complex projects.
• Strong analytical skills with the ability to identify trends and drive improvement initiatives.
• Excellent communication skills, capable of sharing information clearly and supporting cross-functional teams.
• Experience with investigations, CAPA, complaint handling, and data trending.
• Ability to manage multiple priorities and see projects through to completion.

Responsibilities

• Lead investigations and CAPA activities to address quality issues.
• Manage quality data trends and derive actionable insights.
• Collaborate across QA, manufacturing, and other departments to uphold standards.
• Support day-to-day manufacturing operations with compliant documentation.
• Drive continuous improvement initiatives within a regulated setting.

Skills

Quality management

Data trending

CAPA investigations

Cross-functional collaboration

Analytical skills

Documentation and compliance

Project management

Education

Bachelor's degree in quality, engineering, microbiology, or related field

Job description

Planet Pharma is seeking a Quality Engineer II to strengthen manufacturing quality and ensure product integrity in a fast-paced, regulated environment. You will contribute to investigations, CAPA, data trend analysis, and cross-functional collaboration to drive continuous improvement.

In this role, you will support day-to-day manufacturing activities, maintain documentation, and uphold quality systems while communicating findings clearly to teams across QA, manufacturing, and compliance