QA Associate
at Johnson Johnson
Beerse, Vlaanderen, Belgium -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 09 Jul, 2024 | Not Specified | 10 Apr, 2024 | 2 year(s) or above | Pharmaceutical Industry,Difficult Situations,Presentation Skills | No | No |
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Description:
Within Johnson & Johnson Innovative Medicine we are recruiting a Quality Associate for Investigational Medicinal Products (IMP) as member of our QA Clinical Supply Chain (QA CSC) team based in Belgium.
In the Research & Development area we develop treatments that improve the health and lifestyles of people worldwide. R&D development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, pulmonary hypertension and reproductive medicine.
Our department, QA CSC, is responsible for the release and certification of Investigational Medicinal Products used in worldwide clinical trials.
As QA CSC Associate, you will support the clinical release and quality oversight process of IMPs so that patient safety and compliance with applicable regulations are warranted.
The Janssen portfolio is continuously evolving, growing and therefore the QA CSC - IMP RCC sub-team is looking for a QA Associate to strengthen the team in execution of the Regulatory Compliance Check.
Are you interested in joining a team that is positively impacting patients’ lives by ensuring high quality in our innovative products?
Are you data and document savvy? Do you have continuous improvement mindset? Do you have an affinity with systems? Do you easily connect & is a good team spirit important to you … this position is waiting for you!
QUALIFICATIONS
Job Qualifications
- University degree, scientific orientation (pharmaceutical, chemical or biological sciences) with at least 2 years experience in the pharmaceutical industry.
- Proven ability to work independently while staying connected with stakeholders.
- Ability to quickly assimilate new technologies and system affinity.
- In-depth knowledge in cGMP (domestic & international), J&J policies, standards and procedures.
- Experience with Quality Systems.
- Demonstrated ability to work across organizational boundaries through influencingand partnering. Communication and presentation skills across all levels are important.
- Understands the business implications regarding quality positions and decisions. Understands the bigger picture.
- Able to think outside the box and come up with innovative and creative solutions to problems. Open-minded for new ideas and willing to pivot when necessary.
- Able to adjust plans and priorities when circumstances change, to prioritize tasks and manage time effectively, and to show resilience in difficult situations.
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Software Testing, Clinical Pharmacy
Graduate
The pharmaceutical industry
Proficient
1
Beerse, Belgium