Training Client Manager, Holly Springs

Posted 2 Days Ago
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Holly Springs, NC, USA
In-Office
94K-174K Annually
Senior level
Healthtech • Biotech
The Role
Develops and maintains training curricula, e-learning, instructor-led, and on-the-job training for GMP manufacturing functions. Partners with SMEs and site leaders to identify needs, assess performance gaps, ensure SOP and regulatory alignment, and evaluate effectiveness. Supports VR, AR, and digital learning strategies, onboarding, role-based training assignments, continuous improvement, audits, and training record retrieval. Requires strong instructional design, adult learning, project coordination, communication, organization, and problem-solving skills.
Summary Generated by Built In

Welcome to Holly Springs, North Carolina— home to Genentech's largest-ever investment with an ambitious goal to be a fully connected Plant of the Future. This is where next-generation technology, capability, digital connectivity and Operational Excellence converge to create the global standard for high-volume, highly-efficient Drug Product manufacturing. This will include Component Prep & Compounding, Liquid PFS Filling, Automated Inspection, Autoinjector Assembly, Packaging/Finished Products. The facility's core is defined by innovation - leveraging advanced automation, robotics, digital tools, real-time data analytics, and simple, streamlined processes to produce the highest quality medicines. This plant will not only meet today’s demand for CVRM (Cardiovascular, Renal, and Metabolism) medicines but is a strategic commitment to be scalable with this portfolio, which serves one of the largest patient populations in the world. This is a fast-paced, highly entrepreneurial environment with a high-level of accountability from the site team to launch operations in 2028. 


Are you a problem-solver and change agent who thrives in a High-Performing Team environment, eager to tackle the most complex manufacturing challenges? If so, this is a once-in-a-lifetime opportunity to not only launch a state-of-the-art facility from the ground-up but to shape the culture of our organization for the next generation. 


Join us in Holly Springs, where you won't just build a plant—you will build the future of medicine


The Opportunity:


In this exciting position, you will support, create, develop, and implement site-specific training content, process ownership, and problem-solving as they relate to training, learning, and development efforts for Holly Springs (HSP) manufacturing site. Additionally, you will support technical capabilities, managing onboarding programs, and effectively ramping up and continuously upskilling staff at Holly Springs.


  • You will develop and maintain departmental curricula, e-learning, instructor-led training (ILT), and On-the-Job Training (OJT) materials for supported operational departments including Quality, Manufacturing, MSAT, Assembly/Packaging, Warehouse, and Engineering.
  • You will partner with Subject Matter Experts (SMEs) and site functional leaders to identify training needs, conduct performance gap analyses, and evaluate training program effectiveness.
  • You will partner with cross-functional departments across the entire site to support the alignment of site training materials with Standard Operating Procedures (SOPs), site documents, operational processes, and GMP compliance standards.
  • You will support the development, integration, and maintenance of Virtual Reality (VR), Augmented Reality (AR), and digital/virtual training strategies across site operational areas to enhance technical capability building.
  • You will drive continuous improvement in areas of ownership and actively participate in broader problem-solving efforts for site and network technical training and digital learning tool initiatives.
  • You will serve as backup facilitator for the Holly Springs New Hire Orientation (NHO) program, supporting scheduling, content updates, and delivery of foundational onboarding modules.
  • You will support the identification, assignment, and tracking of initial role-based training assignments and onboarding progress for staff across supported operational functions.
  • You will support audits and regulatory inspections and retrieval of technical training, qualification, and curriculum records upon request.

Who you are:


  • You have a Bachelor’s degree plus five years of related work experience, with project/program coordination experience in a GMP manufacturing facility. 
  • Possesses a solid understanding of Good Manufacturing Practice (GMP) requirements and regulatory compliance
  • Capable of being a productive team member, executing tasks, supporting alignment, and leading projects that involve cross-functional and/or cross-site collaboration.
  • Written and verbal communication is professional and appropriate for the target audience; understands roles and responsibilities and actively seeks clarification where needed, with the ability to think and work independently.
  • Executes within established timelines and is accountable for results. Demonstrates excellent organization, good judgment, and problem-solving skills. 
  • Possesses the ability to prioritize and organize a high volume of work, ensuring attention to detail and accuracy.
  • Strong knowledge of instructional design methodologies, adult learning principles, and course development models (e.g., ADDIE, SAM).

The expected salary range for this position based on the primary location for this position is $94,000 - $174,000.  Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.


Link to Benefits


This position is eligible for relocation benefits. It is not eligible for full time remote work arrangements.

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Skills Required

  • Bachelor's degree
  • Five years of related work experience
  • Project or program coordination experience in a GMP manufacturing facility
  • Understanding of Good Manufacturing Practice requirements and regulatory compliance
  • Ability to support and lead cross-functional or cross-site projects
  • Professional written and verbal communication skills
  • Independent judgment, organization, prioritization, and problem-solving skills
  • Knowledge of instructional design methodologies and adult learning principles
  • Knowledge of course development models such as ADDIE or SAM

Genentech Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Genentech and has not been reviewed or approved by Genentech.

  • Healthcare Strength — Health coverage is described as comprehensive across medical, dental, vision, mental health, and prescriptions, supported by HSAs/FSAs and broad wellness resources. On‑site fitness and health centers, mental‑health clinicians, and specialized programs like fully covered preventive cancer screenings and menopause support deepen the offering.
  • Retirement Support — Retirement benefits feature a 401(k) with up to a 4% company match plus an additional annual 6% company contribution to eligible pay. Additional financial protections such as life and accident insurance complement salary, bonuses, and stock options.
  • Leave & Time Off Breadth — Time away includes about 20 paid vacation days, paid holidays, personal days, and a year‑end shutdown. A paid six‑week sabbatical every six years notably expands long‑term time‑off flexibility.

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The Company
HQ: South San Francisco, CA
20,069 Employees
Year Founded: 1976

What We Do

Considered the founder of the industry, Genentech, now a member of the Roche Group, has been delivering on the promise of biotechnology for more than 40 years. Genentech is a biotechnology company dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis. We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal. Making a difference in the lives of millions starts when you make a change in yours.

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