At a Glance
- Tasks: Drive GCP project audits and uphold quality processes across various products.
- Company: Join Veeva Systems, a leader in life sciences technology.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborate with global teams in a fast-paced environment.
- Why this job: Make a real impact on compliance and quality in the life sciences sector.
- Qualifications: 3+ years in Clinical QA, strong technical writing skills, and knowledge of GCP guidelines.
The predicted salary is between 51750 - 63250 £ per year.
Veeva Systems, Inc. is seeking a Clinical Compliance Operations Specialist to drive GCP project audits and uphold quality processes across multi-line products and regulated domains. The role collaborates with global teams to promote GCP compliance, author GxP documents, and manage incident remediation.
The ideal candidate has:
- 3+ years in Clinical QA within Life Sciences
- Strong technical writing skills
- A proven ability to navigate ISO 9001/QSRs, GCP guidelines, and CAPA programs in a fast-paced environment
GCP Compliance & Quality Operations Specialist employer: Veeva Systems, Inc.
At Veeva Systems, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our remote MedTech QMS Complaints Lead role offers the flexibility to work from anywhere in the EU or UK, while providing ample opportunities for professional growth and development within a supportive team environment. Join us to make a meaningful impact in the MedTech industry, where your expertise will be valued and your contributions recognised.
