Packaging Operator (GMP)

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.