Pharma Manufacturing Operator – Downstream Production Pro

Johnson & Johnson Innovative Medicine; Haarlemmermeer; On-site; EUR 35,000 - 53,000; Full time

Benefits offered by this job

Varied role

Career development

Quality and safety focus

Job summary

Johnson & Johnson Innovative Medicine in the Netherlands seeks a Manufacturing Operator to support downstream processing of pharmaceutical products. Perform routine production activities per GMP and SOP guidelines, operate and document process steps, and report deviations with accuracy.

You will work in shifts, adapt to changing priorities, and participate in ongoing training. Ideal candidates hold an MBO-2 diploma with 3+ years of experience, or 5+ years with non-relevant qualifications, and

Qualifications

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

Responsibilities

• 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.

Skills

Dutch language proficiency

English language proficiency

Quality oriented

Education

MBO-2 diploma

Tools

MS Office

Job description

Johnson & Johnson Innovative Medicine in the Netherlands seeks a Manufacturing Operator to support downstream processing of pharmaceutical products. Perform routine production activities per GMP and SOP guidelines, operate and document process steps, and report deviations with accuracy.

You will work in shifts, adapt to changing priorities, and participate in ongoing training. Ideal candidates hold an MBO-2 diploma with 3+ years of experience, or 5+ years with non-relevant qualifications, and