Product Quality Lead
- Contractor
- Full-Time
- North Chesterfield, VA
- Splintpharma
- Prefferd visa: OPT, CPT, F1, H4, Have H1 Visa, Need H1 Visa, EAD
- Posted 1 year ago – Accepting applications
-
Offerd Salary $ 25 - $ 40
-
Required Position 2-4 hires
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Experience 0-3 Years Required
Job Opening for Product Quality Lead - Film, North Chesterfield, VA
We are currently working on below mentioned i., e. Job Opening for Global Regulatory Systems Manager, North Chesterfield, VA. Please let me know if you are interested in applying for the same.
Location: North Chesterfield, VA (Hybrid role, 3 days in office, 2 days remote)
Consultant Title: Global Regulatory Systems Manager
Duration: Temp to Perm opportunity
Day to day responsibilities:
Ideal consultant will need regulatory environment/application. Skillset in IT. Project Management -In depth knowledge in Veeva and is subsidiaries; Veeva submission platform and Veeva RIMS
Regulatory operation experience and working with regulatory affairs within all elements of regulatory systems i.e.: Adobe, ISI toolbox, Iquivia RIMsmart
In depth knowledge on validation, writing scripts, working in conjunction with IT department
Project management skillset (MS Project is a plus), coordination, internal regulatory affairs, specs/requirements. Work with operation colleagues (strong interpersonal skills)
Good with timelines, management, coordination efforts, expectations
Working with a variety of people within Indivior operation or pharmaceutical industry
Job Opening for Product Quality Lead - Film, North Chesterfield, VA
We are currently working on below mentioned i., e. Job Opening for Global Regulatory Systems Manager, North Chesterfield, VA. Please let me know if you are interested in applying for the same.
Location: North Chesterfield, VA (Hybrid role, 3 days in office, 2 days remote)
Consultant Title: Global Regulatory Systems Manager
Duration: Temp to Perm opportunity
Day to day responsibilities:
Ideal consultant will need regulatory environment/application. Skillset in IT. Project Management -In depth knowledge in Veeva and is subsidiaries; Veeva submission platform and Veeva RIMS
Regulatory operation experience and working with regulatory affairs within all elements of regulatory systems i.e.: Adobe, ISI toolbox, Iquivia RIMsmart
In depth knowledge on validation, writing scripts, working in conjunction with IT department
Project management skillset (MS Project is a plus), coordination, internal regulatory affairs, specs/requirements. Work with operation colleagues (strong interpersonal skills)
Good with timelines, management, coordination efforts, expectations
Working with a variety of people within Indivior operation or pharmaceutical industry