The Company
The company is a global biotechnology company dedicated to improving the lives of patients. In Breda they focus on preparing, planning, and coordinating the shipping and distribution of clinical trial materials.
Role Description
As a Manufacturing Technician working on a 3-shift roster, you will be responsible for operating high-tech production lines in a GMP-regulated environment. You will play a key role in ensuring the timely delivery of high-quality pharmaceutical products. This position is ideal for a results-oriented professional with strong technical and analytical skills, a commitment to quality, and a proactive mindset focused on continuous improvement and operational excellence.
Responsibilities
- Operating and monitoring semi-automated production lines in compliance with GMP standards and standard operating procedures.
- Executing production tasks efficiently, ensuring adherence to planned performance targets and product quality standards.
- Performing equipment changeovers, monitoring process parameters, and responding proactively to deviations.
- Collecting, documenting, and analyzing process data using SAP/MES systems.
- Collaborating closely with team members, line leads, and supervisors to ensure smooth operations and effective communication.
- Identifying and implementing process improvements using LEAN and Six Sigma methodologies.
- Managing administrative and logistical tasks related to production.
- Ensuring proper escalation of atypical events and complete thorough shift handovers.
- Participating in troubleshooting and continuous improvement initiatives.
Requirements
- Min 5 years in a manufacturing environment, preferably within GMP/GDP or ISO-certified settings.
- Min 5 years of experience with LEAN manufacturing, Six Sigma, and continuous improvement tools (e.g., 5WHY, RCA, Kaizen, Poka Yoke, TPM, SMED).
- Certified in Lean/Six Sigma (Yellow or Green Belt preferred).
- Proficient in ERP systems such as SAP and MES.
- Familiarity with Standard Operating Procedures and data-driven process control.
- MBO in a technical or process-related field and/or VAPRO A/B certification.
- Additional training in Advanced LEAN and/or Six Sigma.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Strong communication skills in both Dutch and English (written and verbal).
- Team-oriented, structured, and detail-focused.
- Demonstrates ownership, accountability, and a strong sense of responsibility.
- Analytical thinker with a continuous improvement mindset.
- Flexible with working hours, including shifts, overtime, and weekends.
- Open to change, proactive, and capable of working independently on improvement projects.
- Culturally aware and effective in diverse team environments.
Other information
Apply to our vacancy for more information. Looking forward to getting in touch!
56633
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About us
Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.
SIRE Life Sciences is proud of its ability to adapt to changing trends while always maintaining the highest level of quality for both our clients and our candidates.
Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.
Effective employment solutions need to put the right person in the relevant place every time, using advanced systems to streamline costs and time-frames for clients.