GMP Manufacturing Associate — Quality & Shift

SIRE LIFE SCIENCES; Breda; On-site; EUR 32,000 - 42,000; Full time

Job summary

SIRE LIFE SCIENCES, a global pharmaceutical manufacturer, seeks a Pharmaceutical Manufacturing Associate to support GMP‑regulated production. You will follow approved procedures, perform manual/semiautomated tasks, and execute quality checks across batch records and production logs.

You will collaborate with Production and Quality Assurance teams to ensure safety, compliance, and continuous improvement in a structured, process-driven environment.

Qualifications

• Minimum 2 years on manual and/or semi-automated production lines.
• Experience in a GMP-regulated environment is highly preferred.
• Strong understanding of SOPs and quality standards.
• Fluent in English, written and verbal.

Responsibilities

• Execute manufacturing activities per SOPs and GMP regulations.
• Perform manual production and operational tasks to support processes.
• Conduct in-process quality checks for product quality and compliance.
• Accurately complete batch records, logbooks and production documentation.
• Identify, report, and support investigation of deviations and quality issues.
• Assist with equipment preparation, setup, cleaning and maintenance.
• Support production changeovers and readiness activities.
• Maintain clean, organized, audit-ready manufacturing areas.
• Follow all safety, quality and compliance requirements.
• Collaborate with Production, QA and cross-functional teams to meet goals.
• Participate in continuous improvement initiatives and meetings.
• Proactively address problems to improve efficiency.

Skills

GMP compliance

SOP adherence

Attention to detail

Teamwork

Communication

Documentation

English fluency

Job description

SIRE LIFE SCIENCES, a global pharmaceutical manufacturer, seeks a Pharmaceutical Manufacturing Associate to support GMP‑regulated production. You will follow approved procedures, perform manual/semiautomated tasks, and execute quality checks across batch records and production logs.

You will collaborate with Production and Quality Assurance teams to ensure safety, compliance, and continuous improvement in a structured, process-driven environment.