Facilities Engineering Lead, CVRM (Holly Springs)

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:

We're seeking a highly experienced and strategic Facilities Engineering Lead to oversee all facilities-related operations at our state-of-the-art manufacturing site. This critical role ensures the continuous, compliant, and efficient operation of all plant infrastructure, utilities, and services to support cGMP manufacturing activities.

During the plant start-up project you will act as User Team Lead for Facilities owned systems and be accountable for implementing all global asset management processes and ensuring appropriate criticality, FMEA, and preventive maintenance programs are in place. In partnership with the Engineering and the start-up project (user) team you will partner and collaborate with our partner organizations (Engineering and MSAT, Quality, Supply Chain, Technical Development, Regulatory, CMO, Strategy) to provide expertise in project management and technical design, testing, qualification, validation, as well as all other activities related to design and start-up a new Drug Product Fill and Finish facility.

As part of plant start-up you will act as the Facilities ASSET main functional contact (MFC) for the SAP ERP deployment; responsible for the timeline, deliverables, and adherence to the global template processes.

Initially, you will perform a mix of remote and onsite work (first at the General Planner's office, later at construction site/plant). You will transition to local full time on-site work once the site buildings are built and equipment delivered. Travel of up to 30% of the time is expected during the project phase.

• You will drive optimal greenfield facility and operations design towards high manufacturing efficiency and quality in line with product and regulatory requirements. You will champion self-initiated or assigned parts of the project within the context of project and company objectives, and justify goals towards management. This also includes provision and realization of creative ideas to drive business and project efficiency and may contain connecting manufacturing technology advances and digital transformation aspects. Presents ideas, project goals, progress, risks, and results across departments, to senior management, and at international meetings.

• You will develop and execute a comprehensive Facilities Management strategy aligned with the site's manufacturing goals, regulatory requirements, and capital improvement plans. This includes ensuring all facility operations, documentation, programs (e.g. Calibration and Preventative Maintenance) and infrastructure (e.g., HVAC, cleanrooms, utilities, water systems, electrical systems) are maintained in a validated and compliant state according to cGMP, FDA, EMA, and local regulations.

• You understand the bigger picture of the project and the CVRM disease area and how PT contributes to it. Works closely with the overall project team, the wider organisation and interdepartmental staff to meet department and company goals. Effectively partners with and influences stakeholders across the organization without formal authority, and drives technical decisions balancing product, site, and operations views.

• You will provide leadership for involved project teams and across the broader organisation. Provides training materials and training for people joining the organisation. Acts as a coach for colleagues with less experience and helps them develop skills/expertise.

• You will ensure the integration of environmental health, safety, and security into the business processes, systems, and programs while reporting safety and environmental incidents within one's functional area. Fosters a safe and compliant speak up culture. Actively build, support, and promote a culture of continuous improvement and learning from both successes and failures.

• You will design and execute studies and comparability protocols to support the required operations. You will contribute to cGMP documentation and regulatory filings.

Who You Are:

• You hold a Bachelor's Degree in Engineering (preferred)

• You have 12+ years of work experience in the pharmaceutical or related industry with direct experience in cGMP regulated environment.

• You have knowledge and experience managing equipment, facility, and utility (EFU) or other complex execution-based organizations with competing priorities.

• You have updated knowledge of cGMP's, Health Authority regulations, and Quality Systems.

• You have an ability to organize and solve complex, unique or unprecedented problems through the regular use of ingenuity and innovation; consistently demonstrates courage and drive to ensure optimal business results.

• You have experience working with collaborators, regulatory agencies, and vendors inside and outside the company including coordination across organizational lines, including advising and influencing senior management on advanced technical matters. Utilizes an established network for technical issues within the company and the industry.

• You have strong organizational and interpersonal skills: can get things done in a way that optimizes results, strengthens internal and external relationships, and with consideration of resources. Is able to coach others.

Work Environment/Safety Considerations:

• Ability to work in an international/global environment. Domestic and international travel required. Travel up to 20% after full relocation.

• May work in the clean room environment that requires gowning in the form of hospital scrubs, bunny suits, gloves, and steel toe boots.

• Potential to work near hazardous materials, chemicals, and equipment as per company safety procedures and guidelines.

Relocation funding is available for this role.

The expected salary range for this position based on the primary location of Holly Springs, North Carolina for a Senior Principal Engineer with 12-14 years of experience is $114,400 - $212,400. For a Distinguished Engineer with 15+ years of experience the salary range is $138,300 - $256,800.

Actual pay will be determined based on experience, 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.

Benefits

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.