3 дня назад
Associate, Quality Records
64 600 - 107 600$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate, Quality Records (Quality Systems/Regulatory Compliance): Managing electronic document workflows, records governance, and ELN administration for Research & Development Vaccines programs with an accent on compliance, archival controls, data integrity, and stakeholder enablement. Focus on administering systems such as GDMS, Gnosis, Veeva, ValGenesis, and Signals, supporting audit readiness, and implementing AI-enabled workflow automation.
Location: Hybrid in Pearl River, New York, United States. Candidates must have permanent U.S. work authorization; U.S. work visa sponsorship is not available.
Annual base salary: $64,600–$107,600, plus eligibility for a 7.5% bonus target.
Company
develops medicines and vaccines and supports regulated research and development programs focused on improving patient care.
What you will do
- Manage electronic workflows for creating, reviewing, approving, and archiving controlled documents supporting Vaccines programs.
- Execute document control activities, including metadata assignment, version control, status tracking, and lifecycle management.
- Administer Electronic Laboratory Notebook operations, including user access, onboarding, troubleshooting, templates, compliance monitoring, and system enhancements.
- Support records governance, retention practices, audit readiness, data integrity, and applicable GLP and GCLP requirements.
- Provide training, guidance, and customer support to scientific stakeholders, including senior leadership.
- Identify process bottlenecks and implement AI-enabled, automated, and digital solutions to simplify workflows.
Requirements
- Bachelor's degree in a scientific, technical, business-related, or relevant discipline.
- Advanced proficiency in Microsoft Office Suite and Adobe Acrobat Professional.
- Strong communication, organization, planning, time management, and attention-to-detail skills.
- Ability to work independently, collaborate across organizational levels, and manage multiple priorities.
- Technology fluency and the ability to adopt AI-enabled and digital solutions for workflow improvement.
- Permanent U.S. work authorization is required; visa sponsorship is not available.
Nice to have
- Experience in pharmaceutical, biotechnology, medical device, life sciences, or another highly regulated environment.
- Experience with GDMS, Veeva Vault, ValGenesis, Gnosis, or similar electronic document management platforms.
- Knowledge of document control, records management, archiving, and GxP requirements such as GLP, GCP, or GCLP.
- Experience with AI-assisted tools, automation solutions, or digital productivity platforms.
Culture & Benefits
- Hybrid work arrangement supporting Vaccines research and development programs.
- Comprehensive medical, prescription drug, dental, and vision coverage.
- 401(k) matching contributions and an additional retirement savings contribution.
- Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
- Participation in 's Global Performance Plan with a 7.5% bonus target.
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