Job Title: Manager GCP Quality, Technology and Compliance
We are seeking a quality-focused systems expert to shape our approach to managing regulated processes across Global Development.
Key Responsibilities:
* Manage and triage user requests via the Quality Support Mailbox
* Coordinate eQMS system upgrades and configuration changes with Global Development IT
* Support issue management workflows including deviations, CAPAs, investigations, and change controls
* Gather and refine business requirements to guide system enhancements
* Create dashboards, storyboards, and reports for audit readiness and quality oversight
* Liaise with stakeholders across Clinical, Regulatory, Medical, and Quality functions
This role requires expertise in managing quality workflows, system lifecycles, and regulated processes. The ideal candidate has experience with the Veeva Quality Suite, particularly QualityDocs and QMS modules, and is familiar with GCP and/or GVP-regulated processes.
Required Skills and Qualifications:
* Quality workflow management
* Regulated process expertise
* Veeva Quality Suite experience
* System lifecycle management
* Audit readiness and quality oversight
The ideal candidate will have a strong understanding of quality principles and practices, as well as experience working with regulated processes and systems. They will be able to work effectively in a team environment and communicate complex technical information to both technical and non-technical stakeholders.
Benefits:
This role offers a competitive salary and benefits package, as well as opportunities for professional growth and development. We are committed to providing a supportive and collaborative work environment that allows our employees to thrive.
How to Apply:
Interested candidates should submit their resume and a cover letter outlining their qualifications and experience. We look forward to hearing from you!