Are you passionate about quality and precision? Join our client as QA Specialist and help ensure top-tier standards every day.
Hobson Prior is seeking a QA Specialist to provide quality and compliance support to scientific teams and assist throughout the drug development process. This position is ideal for someone passionate about ensuring high-quality standards in pharmaceutical development and manufacturing.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Ensure the quality release of manufactured drug products for clinical trials.
- Assist with investigations and decisions related to quality and compliance in drug development projects.
- Offer proactive quality advice to improve GMP quality systems and implement global standards.
- Collaborate with global teams to create unified processes and practices.
Key Skills and Requirements:
- Background in pharmacy or engineering with a focus on pharmaceuticals.
- Familiarity with international quality regulations and industry practices.
- Strong understanding of GMP regulations and the pharmaceutical development process.
For more information, please contact Lisa Venn.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -https://www.hobsonprior.com/privacy-policy?nav=e9d7b594-f5cb-45e1-06b2-08d71b498662
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