Quality Control Analyst II

F. Hoffmann-La Roche AG; South San Francisco (CA); On-site; USD 79,000 - 146,000; Full time

Benefits offered by this job

Discretionary annual bonus

Benefits package

Job summary

Genentech, a member of the Roche group, seeks a Lab Analyst to join Global Analytical Development and Quality Control. You will perform physico-chemical tests for biologics per GMP and help maintain inspection readiness while supporting project teams and customers.

Requires a Bachelor's in a scientific field or an Associate's with 5 years in a lab, plus clear communication and strong problem-solving. Relocation is not offered; a discretionary annual bonus may apply.

Qualifications

• Clear communication and written skills required.
• Attention to detail and strong organizational ability.
• Ability to work effectively in a collaborative team.

Responsibilities

• Perform basic to moderately complex physico-chemical tests for biologics and other compounds per GMP.
• Maintain inspection readiness and accurate documentation in systems.
• Coordinate with customers to support operations and participate in group projects.

Skills

Clear communication

Attention to detail

Teamwork

Problem-solving

Education

Bachelor's degree in science

Associate's degree + 5 yrs lab experience

Job description

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.

The Opportunity

You perform a broad variety of basic and moderately complex physico-chemical 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.

Who you are

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.

Benefits

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.

Who We Are

Genentech, a member of the Roche group and founder of the biotechnology industry, is dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. To solve the world's most complex health challenges, we ask bigger questions that challenge our industry and the boundaries of science to transform society. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis. The next step is yours.

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.