Job description
Proclinical is seeking a Veeva Vault QMS Senior Manager for a global pharmaceutical company located in Watertown, MA.
Must be eligible to work in the US.
Job Responsibilities:
- Oversight and Support of Quality Event and Actions (Deviations, CAPA, Change Control, Change Actions and Proactive Initiatives), including both operational and maintenance activities.
- Manage Veeva Vault QMS modules, ensuring system continues in a validated state. This includes representing Veeva QMS as business owner to trouble-shoot and test user/application related issues and new system functionality/releases.
- Provide and execute innovative ideas to compliantly advance document process efficiencies, training effectiveness and sharing of best practices.
- Own and maintain relevant procedures and supporting documentation for QMS.
- Identify quality issues/discrepancies, and effectively and proactively resolve them in a diplomatic, flexible, and constructive manner.
- Serve as Veeva QMS Admin
Skills and Requirements:
- BA or BS degree or equivalent industry experience
- Minimum of 5 years of Quality Systems functional experience in a regulated industry
- Veeva Quality Suite and Platform experience required
- Previous experience executing computer system validation deliverables such as User Requirements Specifications and qualification scripts
- Inspection Readiness experience preferred.
- Excellent verbal, written, and presentation skills with the ability to deal effectively across all functional areas
- Able to provide solution minded approach and flexibility to emerging challenges
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at (+1) 215-531-6914 or s.briggs@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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