BeiGene, Ltd.

Manager, GMP Training

BeiGene, Ltd.$79K — $109K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences, Quality, Education, Business, or related field; Master's preferred.
  • 5+ years in biotechnology/pharmaceutical industry managing GMP training programs.
  • Strong knowledge of GMP requirements and FDA expectations.
  • Experience with regulatory inspections and audit readiness.
  • Ability in training effectiveness assessments and risk-based strategies.
  • Proven project management skills in training during organizational changes.
  • Excellent communication and collaboration abilities.

Responsibilities

  • Lead and improve the GMP Training Program to meet regulatory and operational needs.
  • Act as SME during inspections and audits.
  • Support implementation and upgrades of eLMS tools.
  • Develop a Train-the-Trainer Program to empower internal trainers.
  • Create and maintain comprehensive training curricula and matrices.
  • Drive compliance improvements and training effectiveness across departments.
  • Monitor training metrics to identify trends and risks.

Benefits

  • Comprehensive medical, dental, and vision plans.
  • 401(k) with company matching contributions.
  • Flexible spending account/health savings account options.
  • Life insurance coverage.
  • Generous paid time off policy.
  • Employee wellness programs.
  • Equity awards for all employees.
Full Job Description
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 the Job:
  • 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.
  • Lead cross-functional efforts to improve training compliance, reduce overdue training, and enhance overall training effectiveness.
  • Establish and maintain training strategies, processes, and governance to ensure employees receive role-appropriate training.
  • Develop and monitor training metrics and key performance indicators to identify trends, risks, and improvement opportunities.
  • Collaborate with functional areas to investigate training-related deviations, CAPAs, audit observations, and compliance gaps, and ensure appropriate corrective actions are implemented.
  • Set standards for training content, effectiveness assessments, and qualification activities.
  • Prepare training reports and management-level presentations that communicate program performance, compliance status, and emerging risks.
  • Perform other duties as assigned by management.


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 with Clarity


Salary Range: $79,600.00 - $109,600.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

About BeiGene, Ltd.

BeiGene, Ltd. is a biotechnology company that develops and commercializes innovative cancer treatments. The company was founded in 2010 and is headquartered in George Town, Grand Cayman. BeiGene's portfolio includes several drug candidates that target cancer cells and the tumor microenvironment. The company's lead product, Brukinsa, is a treatment for mantle cell lymphoma that has been approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). BeiGene also has partnerships with several pharmaceutical companies, including Amgen, Merck, and Novartis.
Learn more about BeiGene, Ltd.
Size
8,300 employees
Market Cap
$22.2 billion
Industry
Net Income
-$1.5 billion
Founded
2010
5 Year Trend
+305.7%
Revenue
$308.8 million
NASDAQ

Similar Jobs

More Jobs at BeiGene, Ltd.

More Pharmaceuticals & Biotech Jobs

Find similar Manager, GMP Training jobs: