Job Title: Manufacturing Technical Specialist II / Engineer I
Responsible for providing scientific and technical support to GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. This includes activities related to safety, compliance, quality, targeted innovation, and plant performance and success. Deliverables include but are not limited to implementation of targeted new technologies and procedures, assessing, evaluating and providing immediate corrective actions for GMP discrepancies and intra batch process monitoring, analysis and reporting. May troubleshoot equipment and systems; develop new equipment requirements and operating parameters, providing factory acceptance testing and validation support. Investigates operational and process discrepancies, implements corrective action, and develops and validates manufacturing improvements.
The Engineer I will be an integral member of the Oceanside Laboratory and Pilot Plant (OLP) upstream team.
Perform required operations at pilot and small scale.
Execute and lead small/pilot scale studies in close collaboration with customer and all involved groups to support: make-assess release, tech transfers, and network.
Automation and Engineering Solutions and act as a member of a high functioning team. These tasks will include those associated with coordinating and performing operations (i.e. set up, inoculating, maintaining, harvesting and cleaning equipment/bioreactors)
Experiment data recording, collection, and analysis. He/she should be able to present information timely, clearly, and confidently.
Lead technical transfers of phase III molecules from late stage process development to commercial launch scale and commercial scale to commercial scale: verification of scale-down model and site dependent/facility fit studies.
Lead close communication between late stage process development and molecule recipient commercial site.
Lead technical teams in support of site investigations and commercial make-assess-release.
Lead scale up of processes:
ability to generate feedstock for downstream pilot-scale studies
harvest process parameter range studies (pilot scale)
characterization at pilot scale to ensure optimal operability at large scale: consistency runs (thaw to formulation) and verification of manufacturing process robustness at pilot scale.
Liaison between Operations and the Pilot Plant customers.
Offer technical/operational expertise, attentive customer service, and work as an integral partner in the successful execution of experiments.
Provide and spearhead troubleshooting assistance with equipment and processes
Trainer for other technicians and support personnel.
Specific focus on continuous process improvement, new technology/process implementation and will design experiments and apply theories to execute projects.
Lead and manage independent projects as well as participate on cross-functional teams as a representative of the laboratory and pilot plant upstream team.
The ability to work independently under limited supervision
Coordinating and performing operations and tasks associated with cell culture experiments at pilot and small scale.
Having a solid understanding about CHO processes and experience with analytical instruments is preferred.
The ability to display a strong focus on collaboration, customer service, attention to detail, analytical ability and intellectual curiosity.
Must be able to work on a team with diverse skills and objectives and interact with customers in a productive manner.
Operational and technical troubleshooting skills and creative, flexible problem solving skills are required.
Project coordination/management skills are needed and must have demonstrated the ability to take a project from idea inception to implementation.
Interfacing with customer groups by seeking opportunities for collaboration, and proactively communicating and presenting information timely, clearly, confidently, and concisely and offer relevant views and information to impact decisions.
High level of demonstrated initiative, exhibit flexibility in work approach, and demonstrate strong follow through and accountability.
Must be self-driven to learn and keep current with new technology developments and be organized and capable of multitasking, have effective problem solving abilities, and have demonstrated reliable decision-making.
Demonstrates flexibility to ensure that all cell culture operations at pilot and small scale are supported to meet run schedule demands while managing other areas of responsibility, such as project support.
Bachelor's, Master's, or Ph.D. degree in Chemical/Biochemical Engineering or Life Sciences.
Must have 4 - 6 years of hands-on cell culture experience and a familiarity with pilot plant and lab techniques and processing.
Mechanical aptitude and knowledge and experience with computer systems are also needed.
Must be able to lift up to 40 pounds
This position is not eligible for relocation.
Who We Are
A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry
for more than 40 years, using human genetic information to develop novel medicines for serious and
life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious
illnesses. Please take this opportunity to learn about Genentech where we believe that our employees
are our most important asset & are dedicated to remaining a great place to work.
The next step is yours. To apply today, click on the "Apply online" button.
Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page.