Associate Process Engineer – GMP Manufacturing

Biopharma Careers; Groningen; On-site; EUR 38,000 - 61,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave (12 weeks)

Well-being reimbursement

Job summary

Johnson & Johnson in Groningen is seeking an Associate Process Engineer to support manufacturing, process, and packaging operations with technical execution and continuous improvement.

You will work with cross-functional partners to meet safety, quality, delivery, and cost objectives in regulated environments, contributing to validation and change control while ensuring GDP-compliant documentation.

Qualifications

• Strong analytical problem-solving skills with data analysis and visualization experience.
• Effective written and verbal communication skills.
• Ability to work collaboratively in cross-functional teams.
• Proficiency in producing clear, compliant technical documentation.
• Fluency in English; other languages site-dependent.

Responsibilities

• Provide day-to-day engineering support within assigned manufacturing and process areas.
• Assist in identifying, analyzing, and resolving equipment, process, and product issues using structured problem-solving and data analysis techniques.
• Support troubleshooting to restore and improve process performance, quality, and safety.
• Identify and implement opportunities for process and equipment improvements to enhance efficiency and compliance.
• Participate in validation, change control, and documentation activities to meet regulatory requirements.

Skills

Analytical problem-solving

Communication skills

Cross-functional collaboration

Documentation

Attention to detail

Education

Bachelor’s degree in Engineering or Material Science

Job description

Johnson & Johnson in Groningen is seeking an Associate Process Engineer to support manufacturing, process, and packaging operations with technical execution and continuous improvement.

You will work with cross-functional partners to meet safety, quality, delivery, and cost objectives in regulated environments, contributing to validation and change control while ensuring GDP-compliant documentation.