Quality Control Analyst II - Fixed Term

1000 Genentech, Inc.; United States; On-site; USD 45,000 - 84,000; Full time

Benefits offered by this job

Discretionary annual bonus

Benefits package

Job summary

Genentech, a member of the Roche group, is seeking a QC Analyst II in Oceanside, CA for a fixed-duration 2-year assignment. You will perform routine chemical assays and manage sample workflows to support product quality and patient safety.

In a fast-paced lab, you will maintain instruments, assist with investigations and data trending, and collaborate with cross-functional teams while adhering to GMP, GLP, and safety standards.

Qualifications

• Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry, or related discipline.
• 1–2 years of regulated laboratory experience or equivalent.
• Able to work independently in a fast-paced environment.
• Strong communication and organizational skills.

Responsibilities

• Conduct routine chemical assays and compendial testing per GMP.
• Prepare reagents, manage samples, and maintain inventory.
• Maintain and calibrate analytical instruments and troubleshoot as needed.
• Ensure lab inspection readiness and comply with safety protocols.
• Assist with data review, investigations, and trending.
• Support validations, testing protocols, and cross‑functional projects.

Skills

Regulated laboratory experience

LIMS

Google Workspace

Microsoft Office

Education

Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry, or related scientific discipline

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. This is a fixed duration position for 2 years.

As a QC Analyst II based in Oceanside, you will join our collaborative Quality team dedicated to upholding the highest product safety and analytical standards for our commercial and clinical therapies. In this role, you will conduct critical routine testing and manage analytical workflows that directly impact patients around the world. Working in an agile and fast-paced laboratory setting, you will have continuous opportunities to build your technical skills, expand your expertise, and grow your career.

The Opportunity

• You conduct routine chemical assays and compendial testing (including pH, osmolality, and color) on in-process manufacturing samples per standard procedures and GMP guidelines.
• You prepare laboratory reagents and perform sample management, aliquoting, and inventory control to maintain continuous testing operations.
• You maintain, standardize, and calibrate analytical instruments, helping to troubleshoot chemical assays when challenges arise.
• You ensure the laboratory remains in an inspection‑ready state at all times while following safety and environmental protocols.
• You assist with laboratory investigations, data review, and data trending to support product quality and operational excellence.
• You support the execution of validation studies, specialized testing protocols, and department projects in collaboration with cross‑functional partners.

Who you are

• You hold a Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry, or a related scientific discipline with 1–2 years of regulated laboratory experience (or an Associate degree with 4 years, or a High School diploma/equivalent with 2–4 years of related experience).
• You bring practical knowledge of standard laboratory operations and the ability to work independently in a fast‑paced setting.
• You demonstrate strong interpersonal, verbal, and written communication skills with high organizational aptitude.
• You are comfortable utilizing digital laboratory tools and productivity software, including LIMS, Google Workspace, or Microsoft Office.
• You possess the physical capability to handle laboratory operations, including standing or walking for extended periods, lifting up to 30 lbs, and performing routine hand manipulations.
• Preferred: You have foundational knowledge in GMP, GLP, GDP, and Data Integrity standards.
• You bring proven troubleshooting capabilities for chemical analytical instruments and routine assays.
• You have flexibility to support overtime, weekend, or holiday schedules as needed by business demands.
• Relocation benefits are not available for this posting.

The expected salary range for this position, based on the primary location of California, is $45,200.00 - $83,900.00 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.