Downstream Pharma Operator: GMP-Driven Production

Biopharma Asia; Nederland; Ibrido; EUR 35.000 - 53.000; Tempo pieno

Descrizione del lavoro

Johnson & Johnson is seeking a Manufacturing Operator for downstream processing to support GMP-compliant production. You will operate and monitor process steps, document data, and contribute to continuous improvement in a dynamic team environment.

You should have an MBO-2 with 3+ years or 5+ years non-relevant experience, be fluent in Dutch or English at least B1, and have basic computer skills. This role includes shift work and offers growth within a quality-focused culture.

Competenze

• MBO-2 diploma with at least 3 years of experience, or a non-relevant MBO-2 with at least 5 years of experience.
• You have at least B1 level proficiency in Dutch or English.
• You have basic computer skills (MS Office, business applications).
• You are quality-oriented, accurate, flexible, and have a positive attitude.
• Experience with downstream processing or GMP is a plus.

Mansioni

• Perform routine production activities according to strict GMP and SOP guidelines.
• Operate, monitor, and record various process steps within downstream processing.
• Accurately document process data and report any deviations or improvement ideas.
• Collaborate with colleagues and elevate issues to your supervisor when necessary.
• Contribute actively to continuous improvement and help achieve production and quality goals.
• Complete all required training and keep your knowledge up to date.
• Work in shifts and handle changing priorities with flexibility.

Conoscenze

Accountability

Analytical Reasoning

Collaboration

Continuous Improvement

Demand Forecasting

Detail-Oriented

Distribution Management

DRP

Document Management

Order Management

Pre-Fulfillment Processes

Process Oriented

Project Support

Strategic Supply Chain Management

Technical Credibility

Transportation Management

Warehouse Management

Descrizione del lavoro

Johnson & Johnson is seeking a Manufacturing Operator for downstream processing to support GMP-compliant production. You will operate and monitor process steps, document data, and contribute to continuous improvement in a dynamic team environment.

You should have an MBO-2 with 3+ years or 5+ years non-relevant experience, be fluent in Dutch or English at least B1, and have basic computer skills. This role includes shift work and offers growth within a quality-focused culture.