Warehouse Supervisor, CVRM (Holly Springs)

Genentech; Holly Springs (NC); On-site; USD 83,000 - 153,000; Full time

Benefits offered by this job

Relocation benefits

Discretionary annual bonus

Job summary

Genentech in Holly Springs, NC, is seeking a Warehouse Supervisor to lead a high-volume GMP warehouse during pre- and post-startup phases. You will own SAP/eWM processes, ASRS coordination, and drive Right-First-Time compliance while building a capable foundation team.

You will supervise a team, manage receiving, staging, and shipping, and ensure regulatory readiness with FDA/EMA standards. A relocation-ready, on-site role offers bonus potential and strong career growth.

Qualifications

• Bachelor’s degree in Supply Chain, Logistics, or related field is required.
• 5+ years of GMP warehouse experience and supervisory experience.
• Strong knowledge of SAP/eWM and warehouse processes.
• Familiarity with FDA/EMA/DEA regulations and cGMP requirements.

Responsibilities

• Direct daily warehouse activities, including receiving, staging, and shipping.
• Maintain inventory accuracy through cycle counting and SAP/eWM monitoring.
• Lead investigations into deviations and participate in regulatory audits.

Skills

SAP/eWM

Supervisory experience

GMP knowledge

Regulatory knowledge

Warehouse operations

Education

Bachelor's degree in Supply Chain, Logistics or related

Associate's degree

Tools

ASRS familiarity

Job description

The Position

Pharma Technical Manufacturing (PTM) is responsible for managing all aspects of end-to-end drug substance and drug product manufacturing and supply. From the raw material to the final medicine, we contribute to deliver Roche’s ground-breaking therapies to more than 120 million patients around the world. We make our medicines at 9 sites around the world and coordinate all aspects of production of Roche medicines in all disease areas and dosage forms. To ensure readiness for a step-change in the standard of care that Roche delivers in the area of Cardiovascular, Renal and Metabolism (CVRM), PTM will construct a new manufacturing site in the U.S. in Holly Spring, North Carolina. The new site will focus on large volume low cost Drug Product manufacturing (Component Prep & Compounding, Liquid PFS Filling, Automated Inspection, Autoinjector Assembly, Packaging/Finished Products).

The Opportunity

Pre-Startup:

As the Warehouse Supervisor, you are responsible for the comprehensive and timely ramp-up of all warehouse-related equipment, processes, and systems, ensuring full compliance with cGMP requirements throughout the design, qualification, and validation lifecycle.

The warehouse will be highly automated and this role will act as the business process expert for SAP/eWM, the Automated Storage/Retrieval System (ASRS), and other IT systems for inventory management. This includes defining specifications and processes requirements, testing, local procedure authoring, and training the warehouse team.

• Collaborate with site functions (Quality, Manufacturing, Production Scheduling, Engineering and Maintenance) to ensure successful project completion and efficient operations in the warehouse.
• Provide user input for the build and test phases of eWM implementation and act as SAP/eWM superuser for the warehouse.
• Develop local warehouse procedures where needed and train warehouse personnel on business processes and system transactions.
• Partner with ASRS and Warehouse Control System (WCS) vendors during the commissioning phase to troubleshoot logic errors and optimize throughput bottlenecks before the site go-live.
• Recruit, interview, and onboard the foundation team of warehouse operators, establishing a culture of "Right First Time" compliance early in the project

Post-Startup:

Following the successful go-live and validation, you will transition into the Warehouse Supervisor role responsible for leading a team of warehouse operators running a high volume GMP warehouse.

• Direct daily warehouse activities, including receiving raw materials, staging for production, and shipping finished drug products for CVRM therapies.
• Maintain near-100% inventory accuracy through a rigorous cycle counting program and real-time transaction monitoring within SAP/eWM.
• Lead investigations into warehouse deviations and environmental excursions, serving as the Subject Matter Expert (SME) during internal and external regulatory audits (FDA/EMA).
• Track and report on key performance indicators (KPIs) such as "Dock-to-Stock" time, order fulfillment rates, and safety incident rates to drive continuous improvement.
• Coordinate with Engineering and Maintenance to ensure the ASRS and other automated systems undergo regular preventative maintenance without disrupting production schedules.
• Ensure all warehouse staff are trained on and adhere to OSHA standards and internal safety protocols, particularly regarding automated equipment and high-density storage.

This role will be full time on site at the Holly Springs, NC facility and/or temporary project offices.

Who You Are

You have a bachelor’s degree in Supply Chain, Logistics, or Business Administration or an Associate's degree and 5+ years of relevant GMP warehouse experience.

• Minimum of 2 years of direct supervisory experience or demonstrated lead experience in a high-volume setting.
• Proficient with SAP/eWM or similar warehouse management software and business processes
• In-depth knowledge of pharmaceutical regulations, including FDA, EMA, and DEA requirements.
• Excellent communication and interpersonal skills
• Demonstrated ability to manage complex projects.

Preferred:

• APICS (CPIM) supply chain certification
• Experience working with and managing automated warehouse systems.

The expected salary range for this position based on the primary location for this position of Holly Springs, North Carolina $82,600 - $153,400. 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. Relocation benefits are provided.

Link to Benefits

Relocation Benefits are not provided for this role

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.