NL - Engineer 3, Process

Panda International; Leiden; On-site; EUR 55,000 - 80,000; Full time

Job summary

Panda International in Leiden, Netherlands, is seeking a Process Engineer to maintain and optimize production processes within a GMP-regulated manufacturing environment. You will focus on process reliability, product quality, and operational efficiency in a fast-paced setting.

Start ASAP for a 12-month contract. Responsibilities include introducing new processes, monitoring performance, maintaining SOPs and batch records, and driving continuous improvement with cross-functional teams.

Qualifications

• HBO degree with at least 3 years of relevant experience in process engineering.
• Experience in GMP-regulated pharmaceutical/biotech manufacturing.
• Knowledge of GMP requirements and compliance with manufacturing procedures.
• Experience with process documentation, including SOPs, work instructions, and batch records.
• Knowledge of non-conformance investigations, CAPAs, and change control.
• Strong analytical and problem-solving skills with root-cause analysis.
• Strong communication and collaboration skills; fluent English (B2+).

Responsibilities

• Support the introduction of new production processes and systems.
• Monitor existing processes to minimize downtime and production losses.
• Review and maintain process documentation such as SOPs, work instructions, and batch records.
• Conduct quality risk assessments and product impact assessments.
• Support non-conformance investigations, CAPAs, and change controls.
• Oversee process and equipment qualification activities and collaborate with cross-functional teams.

Skills

GMP knowledge

Process monitoring

Root cause analysis

Analytical skills

Cross-functional collaboration

English fluency

Education

HBO degree

Job description

Process Engineer

Process Engineer Responsible for maintaining, improving, and optimizing production processes within a GMP-regulated manufacturing environment. The role focuses on ensuring process reliability, product quality, operational efficiency, and compliance with applicable regulations.

Responsibilities

Responsibilities include supporting the introduction of new production processes and systems, monitoring existing processes to minimize downtime and production losses, reviewing and maintaining process documentation such as SOPs, work instructions, and batch records, conducting quality risk assessments and product impact assessments, supporting non-conformance investigations, CAPAs, and change controls, overseeing process and equipment performance qualification activities, and collaborating with cross-functional teams to drive continuous improvement and sustainable manufacturing performance.

Non‑Negotiable Skills, Qualifications, and Experience

Relevant HBO degree with at least 3 years of relevant experience Experience in process engineering or a similar role within a production environment Experience working in a GMP-regulated pharmaceutical, biotechnology, or other relevant manufacturing environment Knowledge of GMP requirements and compliance with manufacturing procedures Experience with production process monitoring, troubleshooting, and continuous improvement Experience with process documentation, including SOPs, work instructions, and batch records Knowledge of non‑conformance investigations, CAPAs, and change control Strong analytical and problem-solving skills, including identifying root causes and implementing solutions Strong communication and collaboration skills, with the ability to work with cross-functional teams Fluent English (B2 level or higher)

Desirable Skills, Qualifications, and Experience

Experience with process qualification, performance qualification (PQ), or validation activities Experience conducting quality risk assessments and product impact assessments Knowledge of root cause analysis and deviation management Experience conducting Gemba walks and identifying improvements on the production floor Experience with Lean, Six Sigma, or other continuous improvement methodologies Knowledge of process performance monitoring, yield optimization, and downtime reduction Experience supporting audits and regulatory inspections Strong stakeholder management and documentation skills Ability to manage multiple priorities and work effectively in a changing production environment

Practicalities

Start Date: ASAP
Contract Duration: 12 months
Location: Leiden, Netherlands

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