Deep Learning Specialist developing AI - driven solutions for nature - based assets at climate - tech startup. Collaborating across teams to design and implement ML/DL models for risk and trading signals.
About the role
- Quality Training Coordinator in pharmaceutical sector focusing on training compliance and continuous improvement. Partnering with QA leaders to manage training assignments and maintain records while supporting onboarding initiatives.
Responsibilities
- Administer training assignments, curricula, and compliance tasks in the site Learning Management System (LMS), including SuccessFactors.
- Maintain accurate training records, track overdue requirements, and support remediation efforts.
- Partner with QA and functional leaders on onboarding, OJT documentation, and role-based curriculum mapping.
- Develop, revise, and format training materials such as instructor-led training decks, SOP-driven content, and job aids.
- Generate routine and ad-hoc training compliance reports for stakeholders.
- Support continuous improvement initiatives for training processes, documentation quality, and user experience.
- Coordinate training sessions, logistics, communications, and stakeholder reminders.
Requirements
- Bachelor’s degree in science, engineering, biochemistry, or a related discipline
- 1+ years of experience coordinating or managing training in a GMP/GxP environment, including training assignment creation, compliance tracking, and overdue remediation support
- 2+ years of experience using a Learning Management System (LMS) for training administration (e.g., SuccessFactors, ComplianceWire, Cornerstone)
- 2+ years developing and maintaining SOP-driven training materials, including revising and formatting content and creating job aids
- Knowledge of US and EU cGMP regulations and guidance (FDA, EMA, or other authorities)
- English proficiency sufficient to create training materials and coordinate with stakeholders
- Authorized to work in the United States
- Available to support 2nd and 3rd shift training about once per month for 1–2 hours
Benefits
- Opportunity to work with industry-leading CQV and compliance experts in the pharmaceutical sector.
- Professional development and exposure to advanced training systems and regulatory environments.
- Collaborative team environment focused on quality and continuous improvement.
- Hybrid role for 6 months with potential for contract extension.
- Competitive hourly rate: **$28 – $31.5/hr (W-2 only, no C2C)**
- Working Hours: Monday - Friday, regular business hours
- Health insurance, holiday pay, 401(k) program, and other benefits
- Employee referral bonus program.
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