QA Associate Cryo Lab
il y a 2 semaines
Johnson & Johnson is currently seeking a QA Associate Cryo Lab to join our Cryopreservation team located in Beerse.
Within J&J Innovative Medicine Supply Chain, a member of Johnson & Johnson's Family of Companies, we are recruiting a QA Associate Cryo Lab (M/F/X). The position will be based in Beerse, Belgium.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system. They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, Janssen has constructed two CAR-T manufacturing centers in the Ghent area (Belgium), where CAR-T investigational medicinal and commercial CAR-T products are manufactured. The newly build Cryo Lab will be operated from the existing Janssen Beerse site to provide the manufacturing facilities of their patients starting material.
The QA Associate Cryo Lab works together with the QA Cryopreservation Manager and is accountable for the implementation of the overall EMEA CAR-T quality system in the Cryo Lab including compliance oversight, release of the cryopreserved apheresis material and deviation handling.
What you will be doing:
- Cooperate with the operational technology team and will assist in Quality Assurance Oversight of the daily operations of all incoming fresh apheresis material for cryopreservation to support both clinical and commercial requirements in a new state of the art laboratory.
- Assist in the batch record review and release of the cryopreservation Apheresis products.
- Overview of applicable Quality Agreements and Standards.
- Document Control: Review and approve project-specific documents, including protocols, standard operating procedures (SOPs), batch records, and validation reports.
- Assists the QA Cryopreservation Manager for the establishment and implementation of Company-wide quality policies, strategies and practices.
- Audits & Inspections: Prepare for and participate in internal and external audits and inspections. Lead audit response activities and implement corrective actions as necessary.
- Setting up and maintaining key performance quality indicators.
- Deviation Handling
**Qualifications**:
We would love to hear form you, if you have the following essential requirements:
- A bachelor degree is required. Preferably in medicines, (medical biology), laboratory sciences, or a related discipline such as cell biology, but this is not considered a must.
- Proficiency in English and Dutch (verbal and written), as well as good personal communication skills are required
- Interest or knowledge in cell therapies and oncology is a plus
- Previous experience in a GMP or GTP environment, hospital or blood bank environment is preferred but not a must.
- Good documentation practices is a nice to have
- Soft Skills: Problem-solving mentality and ability to work effectively in cross-functional teams (teamplayer).
Must be open to a flexible work regime, for example: 5pm to 1 am working shift regime.
Training and qualification will be provided in a standard day shift regime.
What type of mark will YOU make?
Diversity, Equity & Inclusion at Johnson & Johnson means "YOU belong"
For more than 130 years, diversity, equity & inclusion have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.
That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued, and every one of our people feels that they belong and can reach their potential. No matter who they are.
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