Hillsboro Technical Operations (HTO) is a manufacturing organization responsible for the reliable delivery of biologics drug product & finished goods, both for Roche's commercial portfolio as well as launch products.

They are joined in their support of Operations by a number of additional functions, including Quality, Safety & Environment, Material Management (Warehousing & Supply Chain), Finance, and People & Culture. All of these groups bring their unique capabilities & perspectives to work together in service of our patients, our employees, and our community.

The Opportunity:

Become a Genentech/Roche leader that inspires all of our people to boldly innovate, collaborate and create outcomes that matter for patients, customers and the company. In this role, you will lead, coach, and develop the exciting and fast-paced Quality Control Operations team in Hillsboro Technical Operations. This includes leading a highly engaged team working in a Good Manufacturing Practices (GMP) environment responsible for maintaining the site's rite to operate.

• You will foster/Promote a positive safety culture that supports continuous improvement through active communication and functional area participation in site safety teams ensuring the safe and efficient operation of assigned functional areas and activities.

• You will schedule and supervise daily and weekly operations for the Quality Control lab.

• You will identify and resolve potential cGMP issues and ensures compliance.

• You will coach and mentor a collaborative team in a dynamic environment

• You will work with management on continuous operational improvement projects and oversees the progress within their area of responsibility.

• You will perform data review/trending

• You will write and/or revise documents (e.g., SOPs, Variances, Deviations, Change Requests) to comply with cGMP practices.

• You will ensure that all operations are performed with 100% compliance to SOPs and cGMP standards.

Who you are:

• You hold a Bachelor's degree (Life Science is preferred) with 5+ years industry experience and 2 years direct leadership experience, or Associate degree with 9+ years industry experience and 2 years direct leadership experience, or High School with 12+ years industry experience and 2 years direct leadership experience.

• You have experience with biopharmaceutical manufacturing facilities (quality control experience preferred)

• You possess knowledge and understanding of cGMPs and familiarity with FDA guidelines.

Work environment:

• You are able to work onsite in an office and laboratory environment.

• You are able to lifting up to 25 lbs

• You are able to work in an environment that requires gowning with gloves and steel toe boots be worn (no makeup or jewelry can be worn when working in the clean room environment)

• You are able to work with hazardous materials and chemicals.

• Note: There are two positions available; both are a 4x10 schedule either Sun-Wed or Wed-Sat (0800-1900)

Relocation benefits are available for this posting.

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