Please note this is a Day Shift position working a 4x10 schedule

Hillsboro Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche’s commercial portfolio & pipeline products.  The Operations organization at HTO is divided into 2 value streams, which combine to produce millions of units of life-saving medicine every year to patients around the world.

The Opportunity:

The Manager Manufacturing (Packaging)  role is a people leadership position, which serves the specialized technical staff responsible for packaging operations at Hillsboro Technical Operations. It is a scheduled shift leadership position, which supports the Finished Goods Value Stream organization as a member of the Value Stream Leadership Team (VSLT). In this capacity, it supports the strategy deployment for the Value Stream, development and coaching of people across the Value Stream and support teams in development of tangible actions to realize business results. The position organizes and prioritizes critical issues and required information for the technical team and collaboration with a cross-functional management team to facilitate efficient decision making necessary to meet customer needs, in alignment with the site goals.

You will enable the safe & reliable delivery of high-quality medicine through the creation of an environment of strong team spirit, timely and effective communications, sense of urgency & highly motivated team.

You will maximize the efficiencies of all business procedures & systems and support the VSLT in the establishment of departmental & Value Stream KPIs.

You will ensure manufacturing of quality products according to Health Authority and Roche Pharmaceutical Quality System requirements, including Discrepancy Management System, CAPA systems, Quality Risk Management and Technical Change Management.

You will monitor and optimize E2E operations and address potential issues when they arise.

You will partner with our supporting functions on staffing related initiatives, process, throughput and schedule optimizations

You will ensure the facility is always inspection-ready through observation, coaching, teaching and upskilling of value stream staff. Foster quality mindset and a culture of compliance with quality systems and regulatory requirements.

You will support, coach and teach team members in development activities that foster a deep understanding and consistent use of lean and agile ways of working, which result in waste reduction and a strong sense of ownership.

You will advocate for Roche’s mission of advancing and boldly championing diversity, equity, and inclusion.

Who you are:

BS with 5+ years’ experience plus 1-3 years of leader experience.

You have strong leadership skills according to Visionary, Architect, Coach, and Catalyst (VACC) model and shown ability to build a forward-thinking outlook; remove barriers, develop people and technical capabilities; build an environment which enables people to perform at their best.

You are able to partner with leadership team to develop the organizational strategies, which ensure the GMP compliance of the site, continuous improvements, and achievement of long-term goals.

You have a strong understanding and engagement of people practices including hiring, promotion, compensation, mentoring, and coaching, and apply these in order to shape the site culture.

You have a strong servant leadership presence and resonant communication at all levels. Experience framing communications for all audiences. Experienced organizational leadership: Proven ability to lead and align an organization with diverse disciplines; experience developing/realizing a vision and multi-year strategies. Passion for developing talent and a culture of innovation, collaboration, and engagement. Demonstrated ability to lead transformation and effectively engage stakeholders.

You are a strategic and systems thinker who proactively anticipates business risks and has a strong drive for execution. Balances need to create an exceptional workforce experience with the need to deliver operational efficiency.

You have advanced knowledge and subject matter expertise in cGMP biologics with an understanding of manufacturing processes, quality systems, and GMP regulations

You have experience with Lean, Six Sigma, Agile, Quality by Design, Business Analytics and SAP experience preferred.

Preferred:

Experience in large scale commercial manufacturing of pharmaceutical drug products is highly desirable.

Experience with pre-filled syringe and/or auto-injector manufacturing operations

The expected salary range for this position based on the primary location for this position of Hillsboro, OR is $92,100 - $171,100 for the Manager level. 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

Relocation benefits are provided

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Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.