Keywords
- HLO/B.Sc.
- Raw material
- Compliance management
- cGMP/SAP/LIMS
Profile
Do you have experience with raw material handling and/or compliance management and do you enjoy working in a multidisciplinary environment with different stakeholders? Then we are looking for you!
This position is part of both the Raw Material and the Compliance Management team of QCD.
Within the Raw Material Team the following tasks include but are not limited to:
- Ordering materials;
- Processing incoming raw materials;
- Perform sampling for raw materials;
- Release testing for raw materials or send out for external testing;
- Releasing materials in eLIMS;
- Accurate completion and review of documentation;
- Ensuring that a high level of quality is maintained in the department;
- Process non-conformance records;
- Lead document revisions;
- Having close contact with stakeholders.
Within the Compliance Management team the following tasks include but are not limited to:
- Lead document revisions;
- Review document revisions;
- Process non-conformance/CAPA records;
- Manage Change Controls;
- Having close contact with stakeholders;
- Potentially manage training curricula of QC employees.
Who we're looking for
The ideal candidate has an HLO/B.Sc. degree (not a Masters) with 2-5 years of work experience with raw material handling and / or compliance management related activities in a pharma/biotech environment. You have affinity with raw materials and experience with quality and laboratory systems such as cGMP, SAP and LIMS.
The candidate fit for the job is accurate, pro-active, a team player and capable of building good relations with all stakeholders.
Department
The Quality Control Development (QCD) labs group is part of the Analytical Development (AD) Department of the Advanced Therapeutics AD sector of J&J Innovative medicine.
The QCD Labs group focuses on supporting production and laboratory activities with:
- Inspection, release and change management of incoming production raw materials, laboratory chemicals and Lab supplies;
- Sample and Material receipt, handling, storage and forwarding;
- Cell Culture services where cells are maintained used for assays and production cell line quality is supported;
- Maintaining controlled state of production clean room and production utilities by environmental and utility monitoring programs and performing safety testing on our products;
- Coordination of Release and Stability testing and Outsource testing;
- Assuring compliance to GMP standard;
- Execution of all internal release and stability testing.
Company profile
At Johnson & Johnson Innovative Medicine, they are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure diseases inspires them. They bring together the best minds and pursue the most promising science.
Additional vacancy information
Reference | : | A2400045 |
Contract | : | Temporary contract with CLS Services |
Education | : | HBO/BSc.
MBO |
Employment terms | : | Project for at least 1 year |
Publication date | : | 31-7-2024 |
Location | : | View location with Google Maps |
Contactperson | : | Claudia Erwich-Faaij |
| | +31 (0)88 22 77 555 |
CLS Services is a leading professional recruitment agency, specialised in the recruitment and secondment of people with a background in chemistry & life sciences.