Pharma Manufacturing Operator (GMP & QC Support)

Biopharma Careers; Leiden; Remote; EUR 35,000 - 53,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Job summary

Johnson & Johnson in Leiden is seeking an Operations Support Contributor for our Manufacturing/Process Operations team. The role focuses on executing routine tasks, maintaining records, and ensuring compliance with GMP and regulatory requirements to support production targets.

The ideal candidate has an MBO-2 degree (or 5 years relevant experience), proficient in Dutch or English, and strong MS Office skills. You will work in a shift-based schedule and contribute to continuous improvement efforts.

Qualifications

• MBO-2 degree or 5 years of relevant experience with a non-related degree.
• Working proficiency (B1 level or higher) in Dutch or English.
• Basic proficiency in MS Office and routine use of business applications.
• Strong attention to detail with a quality-focused mindset.

Responsibilities

• Execute routine operational tasks to meet production targets under general supervision.
• Follow standard operating procedures (SOPs) to support processing of materials and/or pharmaceutical products.
• Ensure compliance with Good Manufacturing Practices (GMP), regulatory requirements, and company policies.
• Monitor resources, identify potential issues, and escalated concerns to leadership as needed.
• Maintain accurate records, track performance metrics, and identify gaps between targets and outcomes.
• Contribute to continuous improvement initiatives to enhance efficiency, quality, and safety.
• Take ownership of personal training and ensure completion of all required learning activities on time.

Skills

Administrative Support

Agile Manufacturing

Analytics Dashboards

Data Compilation

Data Savvy

Process Optimization

Education

MBO-2 degree

Tools

MS Office

Job description

Johnson & Johnson in Leiden is seeking an Operations Support Contributor for our Manufacturing/Process Operations team. The role focuses on executing routine tasks, maintaining records, and ensuring compliance with GMP and regulatory requirements to support production targets.

The ideal candidate has an MBO-2 degree (or 5 years relevant experience), proficient in Dutch or English, and strong MS Office skills. You will work in a shift-based schedule and contribute to continuous improvement efforts.