Pharmaceutical Manufacturing Associate, Breda, Noord-Brabant

Location: Breda, Noord-Brabant  |  Sector: Pharmaceuticals  |  Start Date: 9/18/2026  |  Job ref: 59002

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.


 Other Information
If you are interested and want to apply, please submit your application via the apply button below and contact me.

59002

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Kalyan Raj

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