5714 Automation Engineer
Description:Candidate should be familiar with owning change records, either in Trackwise or Veeva Vault. Candidate should also understand field wiring and loop testing documentation for all impacted instruments, as well as using MS Access 97 database, in order to generate loop diagrams from said database. Candidate would be responsible for […]
6073 Manufacturing GMP Support I
Description:Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in a cGMP manufacturing environment and maintaining areas in a high state of inspection preparedness.Operate and support manufacturing equipment such as the autoclaves to prepare for GMP processing.Maintains records and clean room environment to comply […]
3670 Compliance Administrative Assistant
Duties:Assisting with various Compliance projects including:Maintaining various Office 365/Sharepoint folders by e-filing and organizing documents and reports.Preparation of support materials for briefing our Committees and Sr. Executive partners.This would include calendaring of reminders regarding deadlines for submission of materials, setting meetings to discuss and refine draft materials, and inputting changes […]
5931 Project Manager III
Expectations:Deliver high-value project management core competencies and best practices with high-performing cross-functional teams to achieve technical development milestones on time, on budget, and with high quality. Duties:Manage technical product development teams and projects of moderate to high complexity (e.g. cross-functional, multi-site, global) with a results-oriented mindset.Develop realistic, integrated project plans/schedules […]
5938 QC Analyst I
Description:QC Analyst in QC Microbiology.Responsible for sampling and testing of utility systems and manufacturing process spaces.Perform routine and non-routine sample collection according to cGMPs.Perform a broad variety of basic to complex sample collection and tests in support of lab operations.Perform assays/laboratory maintenance functions.Prepare basic and complex laboratory reagents.Perform data verification […]
3410 Clinical Trial Manager Clinical Operations
Duties: For the assigned study(ies), the Study Manager is accountable for day-to-day Clinical Operations study execution and related deliverables and is the primary point of contact within Clinical Operations for a study. Key responsibilities include managing risks, issues, and opportunities that impact timeline, quality, and budget, overseeing the Clinical Operations […]
6628 Administrative Assistant
Duties:Calendar management for various directors and Executive Director.Scheduling meetings/rooms for meetings with multiple stakeholders across functions.Resolving calendar conflicts.Coordinating logistics for team staff meetings: Preparing the agenda by working with the Director to determine topics and communicating with presenters to confirm/remind them of their presentations. Sending out agenda to meeting participants.Minute […]
8769 EHS&S Specialist 2
Duties: The EHS&S Specialist 2 is a mid-level role in the Environmental, Health, Safety & Sustainability (EHS&S) Department. This position supports the US Region team’s Business Office. This position requires regular onsite work at one or more of the Company’s Northern California offices. ResponsibilitiesSupport implementation of EHS&S programs. Oversees and/or […]
5882 Governance Analyst III
What We DoThe SBO Governance team provides contract monitoring and management for selected Service Providers who deliver critical services and/or have a significant contract value with our overarching goal being to ensure the long-term success of the Service Provider relationship.The primary service categories that are governed by our team include […]
6292 QC Associate II
Job Description: The QC Process Monitoring (QCPM) Associate II is responsible for coordinating and monitoring quality system attributes of QC laboratories, provide technical expertise and provide support for routine make, assess, and release (MAR) operations. The candidate should be able to complete work under minimal supervision, in accordance with cGMP […]