QC Systems Officer
Amsterdam | GMP | SAP | QC Master Data | SAP QM Workflows | + 3 years | Maternity Cover
Your new company
Our client is incredibly proud of its life-saving plasma medicines. Their staff go the extra mile to improve the health of millions of patients worldwide. Are you looking for a position at a flexible, fast-growing company with an interesting history? Then the position of QC Systems Officer in our Quality department is for you! You can count on an attractive, safe and challenging working environment where everyone gets the chance to show the best in themselves. There is also plenty of room to grow, innovate and learn.
Your new role
As a QC Systems officer, you will have a number of key responsibilities which include:
Master Data Setup & Maintenance:
- Define, configure, and maintain QC Master Data in the SAP system, including QC materials, Inspection Plans, and other QC-relevant data.
- Ensure data accuracy, completeness, and compliance with company policies and regulatory requirements
Data Management & Governance:
- Establish and enforce data governance practices for Master Data creation, updates, and deactivation.
- Conduct periodic audits of Master Data to identify and resolve inconsistencies or errors.
- Work closely with cross-functional teams to validate and verify data integrity.
- Act as the Subject-Matter Expert (SME) for SAP QC Master Data and processes.
Quality Control Processes in SAP:
- Develop and implement Catalogues and Selected Sets, Certificate Profile, Inspection Method, Inspection Plans, MICs, Maintenance Plans, Sample Drawing Procedure, Worklist Subscripts and Calculations within the SAP QM module.
- Support the configuration and customisation of SAP QM workflows, including defect recording and corrective action tracking.
Continuous Improvement:
- Identify opportunities for process optimisation related to QC Master Data management and Quality Control.
- Participate in the development and implementation of new SAP functionalities or upgrades.
Reporting & Documentation:
- Generate and analyse quality reports from SAP to monitor performance and identify trends.
- Document standard operating procedures (SOPs) for QC Master Data management and Quality Control processes.
What you'll need to succeed
You have a Bachelor’s degree in Engineering Quality Management, Information Systems, or a related field with 3+ years of experience in Quality Control, QC Master Data management, or a related role within a pharmaceutical manufacturing industry. You are technically proficient in SAP (preferably SAP QM and related modules) and have a strong understanding of quality management systems (GMP or equivalent) with advanced knowledge of Excel and data analysis tools.
What you'll get in return
We offer you an 8-month contract to begin alongside a competitive salary and excellent secondary benefits (including a pension plan).
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.
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Summary
- Job type
- Temporary
- Industry
- Manufacturing & Production
- Location
- Amsterdam
- Specialism
- Life Sciences
- Pay
- Competitive Salary + Travel
- Ref:
- 1049290
Talk to a consultant
Talk to Tom Murphy, the specialist consultant managing this position, located in Amsterdam
Hays Amsterdam, Rijnsburgstraat 9-11
Telephone: 0628837634
JOB_5331132EN1049290