Pharmaceutical Manufacturing Associate

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

About the Company

A global leader in pharmaceutical manufacturing, committed to delivering high-quality healthcare products that improve patients' lives worldwide. The company operates within a highly regulated environment and is dedicated to maintaining the highest standards of quality, compliance, safety, and operational excellence.

Role Description

We are seeking a motivated and detail-oriented Pharmaceutical Manufacturing Associate to join a dynamic production team. In this role, you will be responsible for supporting manufacturing operations in a GMP-regulated environment, ensuring all production activities are carried out in accordance with approved procedures, quality standards, and safety requirements.

Responsibilities

• Execute manufacturing activities in accordance with Standard Operating Procedures (SOPs) and GMP regulations.
• Perform manual production and operational tasks to support manufacturing processes.
• Conduct in-process quality checks to ensure product quality and compliance.
• Accurately complete batch records, logbooks, and production documentation.
• Identify, report, and support the investigation of deviations and quality issues.
• Assist with equipment preparation, setup, cleaning, and maintenance activities.
• Support production changeovers and operational readiness activities.
• Ensure the manufacturing area remains clean, organized, and audit-ready.
• Follow all safety, quality, and compliance requirements at all times.
• Collaborate with Production, Quality Assurance, and other cross-functional teams to achieve operational goals.
• Participate in continuous improvement initiatives and team meetings.
• Maintain a proactive approach to problem-solving and operational efficiency.

Requirements

• Minimum 2 years of experience operating manual and/or semi-automated production lines within a manufacturing environment.
• Experience working within a GMP-regulated environment is highly preferred.
• Good understanding of manufacturing processes, SOPs, and quality standards.
• Fluent in English, both written and verbal.
• Strong attention to detail and commitment to quality.
• Ability to work effectively in a structured and process-driven environment.
• Comfortable performing repetitive tasks with accuracy and consistency.
• Strong teamwork and communication skills.
• Willingness to work in a shift operation.

59002