Pharma Manufacturing Operations Specialist

jj; Leiden; On-site; EUR 35,000 - 53,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave (12 weeks)

Bereavement leave

Caregiver leave

Volunteer leave

Well-being reimbursement

Health programs (financial, physical,

mental health

Service anniversary awards

Insurance plans

Job summary

Johnson & Johnson in Leiden, Netherlands, seeks an experienced Operations Support Contributor to execute routine tasks that back internal operations. The role emphasizes accuracy, timeliness, and adherence to regulatory guidelines while working with professionalism and initiative.

You will follow SOPs, monitor resources, maintain records, and contribute to continuous improvement efforts within a GMP-regulated environment. A shift-based schedule is required.

Qualifications

• MBO-2 level degree with at least 3 years of relevant experience, or 5 years of relevant experience with a non-related degree.
• Proficiency in Dutch or English at B1 level or higher.
• Basic MS Office and business application use.

Responsibilities

• Execute routine operational tasks to meet production targets under general supervision.
• Follow SOPs to support processing of materials and pharmaceutical products.
• Ensure GMP compliance and regulatory requirements.
• Monitor resources and escalate concerns to leadership as needed.
• Maintain records, track performance metrics, and identify gaps.
• Contribute to continuous improvement initiatives for efficiency and quality.
• Own personal training and complete required learning activities on time.

Skills

Administrative support

Attention to detail

Data tracking

Quality mindset

Education

MBO-2 or higher with 3+ years experience

5 years experience with non-related degree

Tools

MS Office

Job description

Johnson & Johnson in Leiden, Netherlands, seeks an experienced Operations Support Contributor to execute routine tasks that back internal operations. The role emphasizes accuracy, timeliness, and adherence to regulatory guidelines while working with professionalism and initiative.

You will follow SOPs, monitor resources, maintain records, and contribute to continuous improvement efforts within a GMP-regulated environment. A shift-based schedule is required.