Process Engineer II

DPS Group Global; Oss; On-site; EUR 65,000 - 82,000; Full time

Job summary

DPS Group Global is seeking a Process Engineer II to support the introduction of new products and processes within a highly regulated manufacturing environment. You will drive technology transfers, process improvements, investigations, and change implementation while collaborating with Operations, Quality, Engineering and Supply Chain teams.

You will apply Lean Six Sigma and Change Management methodologies to identify improvement opportunities, resolve technical challenges, and support

Qualifications

• Experience in pharmaceutical, biotech, medical device or other regulated manufacturing environments.
• Process engineering, manufacturing support or technology transfer experience.
• Knowledge of GMP environments.
• Lean Six Sigma and continuous improvement mindset.
• Strong stakeholder management and problem-solving skills.

Responsibilities

• Support product and process transfers into manufacturing
• Lead and participate in cross-functional investigations, root cause analyses and CAPA activities
• Facilitate process optimization and change implementation projects
• Collaborate with Operations, Quality, Engineering and Supply Chain stakeholders
• Contribute to a culture of operational excellence and continuous improvement

Skills

Process engineering

GMP knowledge

Lean Six Sigma

Stakeholder management

Data-driven decisions

Job description

We are looking for a Process Engineer II to support the introduction of new products and processes within a highly regulated manufacturing environment.

In this role, you will drive technology transfers, process improvements, investigations, and change implementation while working closely with Operations, Quality, Engineering and Supply Chain teams. You will use Lean Six Sigma and Change Management methodologies to identify improvement opportunities, resolve technical challenges, and support data-driven decision making.

Key responsibilities:

• Support product and process transfers into manufacturing
• Lead and participate in cross-functional investigations, root cause analyses and CAPA activities
• Facilitate process optimization and change implementation projects
• Collaborate with Operations, Quality, Engineering and Supply Chain stakeholders
• Contribute to a culture of operational excellence and continuous improvement

Ideal background:

• Experience in pharmaceutical, biotech, medical device or other regulated manufacturing environments
• Process engineering, manufacturing support or technology transfer experience
• Knowledge of GMP environments
• Lean Six Sigma and continuous improvement mindset
• Strong stakeholder management and problem-solving skills