A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche.
In Pharma Technical Development, we actively collaborate and develop creative technical solutions to efficiently transform scientific ideas into products that reliably deliver our pipeline to patients As a Lab Analyst, you will join our Global Analytical Development and Quality Control team, a leader in developing and executing testing methods for our biologics pipeline You will contribute to our mission through innovation, teamwork, and continuous improvement in a dynamic environment
You perform a broad variety of basic and moderately complex physico-che mical tests for biologics and other pharmaceutical compounds according to GMP
You maintain accountability for deliverables affecting department goals and maintain a state of inspection readiness
You identify discrepancies and support the resolution of technical problems to assist the department in meeting corporate objectives
You schedule and execute routine and semi-routine assignments while supporting general lab maintenance operations
You ensure the integration of environmental health, safety, and security into business processes, reporting any safety and environmental incidents within your functional area
You adhere to cGMP policies and procedures, ensuring accurate documentation of activities and transactions in applicable systems
You coordinate with customers to support operational activities and actively participate in group and project teamwork
You possess a Bachelor's degree, preferably in a scientific discipline, or an Associate's degree with 5 years of related experience in a lab environment
You communicate clearly and effectively, both verbally and in writing
You exercise sound judgment, reasoning, and problem-solving capabilities
You demonstrate attention to detail with strong organization and prioritization skills
You take accountability and work effectively as part of a collaborative team
Preferred:
You preferably have previous GMP experience in a biopharmaceutics environment
You possess QC / cGMP experience working in a lab environment in an industry or academic setting
Relocation benefits are not available for this posting
The expected salary range for this position based on the primary location of South San Francisco, CA is 78 500,00 - 145 900,00 USD Annual. Actual pay will be determined based on experience, 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.
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants
About Genentech
We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal.
Making a difference in the lives of millions starts when you make a change in yours. If you’d like to join our team, view our openings at gene.com/careers.
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