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BM
BeOne Medicines
Manager, GMP Training
Career Insights for Compliance Manager
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Based on New Jersey data
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What they do
A Compliance Manager tracks employer compliance with laws and regulations, particularly for organizations in business and health care. Creates company policies, reviews departmental functions and protocol, follows developments in law and regulations affecting the industry
$164,348 / year median in New Jersey
+3% projected growth
Job Description
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
The Manager, GMP Training is responsible for leading the site-wide GMP training program, serving as the subject matter expert (SME), and ensuring that the training program remains compliant, effective, and inspection-ready. The incumbent also functions as the site Business Process Lead (BPL) for global GxP training networks, governance forums, electronic Learning Management System (eLMS) initiatives, and harmonization projects, translating global strategies into actionable site-level implementation plans. This role is located onsite at our Hopewell, NJ site, reporting to the Associate Director, Quality Compliance. Essential Functions of theJob:
Lead, maintain, and continuously improve the site GMP Training Program in alignment with company procedures, regulatory expectations, site objectives, and operational needs. Serve as SME during regulatory inspections, internal audits, and mock inspection activities. Support eLMS implementation and upgrades, including planning, testing and migration. Develop and implement a Train-the-Trainer Program. Develop and maintain site- department
- role
- task
- and qualification-based curricula and associated training matrices.
Qualifications:
Bachelor's degree in Life Sciences, Quality, Education, Business, or related field with 5+ years of experience in the biotechnology, pharmaceutical, or regulated manufacturing industry, including experience managing GMP training programs required; Master's degree and 4+ years of related experience preferred. Experience leading or managing a GMP training program in a regulated manufacturing environment. Strong knowledge of GMP requirements, FDA expectations, and quality systems. Experience supporting regulatory inspections, audits, and inspection readiness efforts. Knowledge of training effectiveness assessments and risk-based training strategies. Experience managing training through major organizational, process, system, or facility changes. Excellent organizational, analytical, communication, and project management skills. Ability to collaborate effectively with employees and leaders across all organizational levels. Strong attention to detail, customer focus, and ability to manage competing priorities and time-sensitive compliance issues.Computer Skills:
Extensive experience with a validated eLMS, preferably ComplianceWire. Experience electronic document management system, preferably Veeva. Advanced proficiency with Smartsheet, Microsoft 365, including, Excel, PowerPoint, Word, Outlook, Teams, and SharePoint. Global Competencies When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates withClarity Salary Range:
$79,600.00- $109,600.
Work Location:
In personBenefits
- Paid Time Off (PTO)
- 401(k) Plans
- Employee Stock Options (ESOs)
- Bonuses/Stipends