Location : Vacaville CA We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements.

Location (mandatory): Portsmouth NH • We are seeking a QC Analyst III will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing and stability studies when needed.

Location - Marana, AZ The global sub-chapter Production Engineering - Change Services is part of the global Engineering Chapter responsible for cost efficient, reliable and lean Change Control Management (ECRs). The scope of this team is mainly on Product Care topics for established products and introduction of new products from pilot phase to commercial production. The sub-chapter brings in technical expertise to deliver successful material, system, process and product changes.

The Data Assurance Associate (GPV) plays a vital role in ensuring the accuracy, compliance, and quality of case processing activities within Pharmacovigilance. This role involves active communication with internal teams, external partners, and vendors to address case-related queries, oversee case corrections, and support training initiatives. The associate will contribute to maintaining the highest standards in pharmacovigilance operations while driving process improvements and compliance with global regulatory requirements.

Location : Vacaville CA Under moderate supervision, QC Specialist is expected to support planning, managing, and executing projects related to the product portfolio for Vacaville Quality Control. These projects include analytical transfers, control system updates, regulatory filings and other activities associated with the life-cycle of a product.

Location - Vacaville California Responsible for support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and Roche/Genentech corporate principals, quality policies, standards and core values. Maintains company’s right to operate, supply to patients, and cost effectiveness by actively participating in continuous improvement projects

Location : Davie, FL 33314 Shift: US time zone 8 hours/day. Willingness and passion to keep things organized, digital literate organization skills and digital literacy should be visible and demonstrate

MES Engineer is responsible for supporting activities such as requirements gathering, testing, implementation and use of Manufacturing Execution Systems (MES). Position is expected to operate with some supervision and some autonomy. Safety

Location (mandatory): Vacaville CA Perform testing of routine and non-routine samples and documents according to GMP. Perform routine lab maintenance.