Requirements: English
Company: DPS Group Global
Region: Hoofddorp , North Holland
Job Title: MSAT Process Engineer I Manufacturing Operations and Compliance Support
About the Job: In your role, you will be responsible for root-cause investigations and continuous improvement initiatives (i.e. CAPAs) for the companies manufacturing site producing T-cell therapy products.
In your new role, you will be:
- Collaborating with technical and operational stakeholders, writing and/or revising SOPs, batch records, and other operations-related documents;
- Investigating and coordinating the resolution of deviations through comprehensive use of Root Cause Analysis tools;
- Devising and implementing CAPAs to address root cause and ensure effectiveness;
- Performing other tasks and duties as assigned by Management.
Requirements
- You have prior work experience in cell culture, cell therapy and/or aseptic processing.
- You have proven technical knowledge & experience with cGMP compliance and you have experience in leading investigations, writing deviation reports, change controls, and corrective actions.
- You possess excellent communication skills and can work in cross-functional teams to obtain project deliverables.
- You have a working knowledge of scientific and engineering principles.
- You are comfortable in a fast-paced expanding company environment and able to adjust workload based upon changing priorities.
- You can function efficiently and independently in a changing environment.
- You are self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description.
- You can think critically and demonstrate troubleshooting and problem-solving skills.
Knowledge and Experience
- You have BSc in Biochemical Engineering, Chemical Engineering, Biotechnology or equivalent; Engineering degree is a strong plus.
- 2-3 years relevant process engineer experience within a Pharmaceutical/GMP Manufacturing Site
- Excellent knowledge of manufacturing processes.
- Strong technical writing skills with experience in protocol/report-writing.
- Strong interpersonal skills