Equipment Operator
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Equipment Operator in Breda, Noord-Brabant, voor een biotechbedrijf, GMP-omgeving, tijdelijke functie.
- Locatie
- Breda
- Werkvorm
- op locatie
- Uren
- 20–24 uur per week
- Contractvorm
- zzp
- Sluitingsdatum
- Eerste waarneming
- Opdrachtgever
- Global biotechnology leader
Eisen
- Experience with Root Cause Analysis (RCA), 5 Why, or other structured problem-solving methodologies
- Strong technical troubleshooting, analytical, and problem-solving skills
- Familiarity with GMP-regulated environments and manufacturing systems such as SAP and MES
- Experience operating automated production, assembly, packaging, or process equipment in a manufacturing environment
- Ability to work independently as well as collaboratively in a fast-paced production environment
- Good communication skills in English and willingness to work in rotating 3-shift or 5-shift schedules
- A proactive mindset with a strong focus on safety, quality, continuous improvement, and operational excellence
Omschrijving
Our client is a global biotechnology leader dedicated to improving patients' lives through innovative medicines. Operating advanced, highly automated manufacturing facilities, the company is committed to quality, safety, innovation, and continuous improvement while offering excellent opportunities for professional growth. As an Equipment Operator, you will operate and optimize automated production and packaging equipment, troubleshoot technical issues, perform minor maintenance, and support continuous improvement initiatives.
Working in a GMP-regulated environment, you will help ensure safe, efficient, and reliable manufacturing while contributing to operational excellence and product quality.
Responsibilities: Manage and oversee automated production and packaging lines, ensuring safe and efficient operations. Perform equipment setup, product changeovers, line clearances, and routine cleaning activities. Diagnose and resolve technical issues to minimize downtime and optimize equipment performance. Carry out minor maintenance tasks and machine adjustments to support operational reliability. Record production activities and performance data using SAP and MES.
Support deviation investigations, root cause analysis (RCA), and continuous improvement initiatives. Ensure compliance with GMP, quality, safety, and operational standards.
Requirements: Experience operating automated production, assembly, packaging, or process equipment in a manufacturing environment. Strong technical troubleshooting, analytical, and problem-solving skills. Experience with Root Cause Analysis (RCA), 5 Why, or other structured problem-solving methodologies. Familiarity with GMP-regulated environments and manufacturing systems such as SAP and MES. A proactive mindset with a strong focus on safety, quality, continuous improvement, and operational excellence.
Ability to work independently as well as collaboratively in a fast-paced production environment. Good communication skills in English and willingness to work in rotating 3-shift or 5-shift schedules.
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