Quality Control Analyst II

Genentech; Oceanside (CA); On-site; USD 45,000 - 84,000; Full time

Job summary

Genentech in Oceanside, CA is seeking a QC Analyst II to ensure safety, quality, and regulatory compliance across manufacturing and products. You will conduct routine and non-routine analyses, calibrate equipment, and generate accurate reports within cGMP/GLP environments.

The role requires a Bachelor’s in Biology or related field with 1 year of experience (AA with 4 years or HS with 6 years). TSA STA clearance is required; you will work with cross‑functional teams and contribute to SOP

Qualifications

• Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry or related field with 1 year of relevant experience (AA with 4 years, or HS diploma with 6 years).
• Proficient in cGMP practices across laboratory assignments and environments.
• Strong teamwork and ability to share responsibilities to complete QC testing efficiently.
• Must be able to pass TSA Security Threat Assessment for warehouse access.

Responsibilities

• Conduct routine and non-routine analysis of the manufacturing environment and in-process products according to SOPs.
• Perform microbiological and chemical assays, basic troubleshooting, and instrument calibration.
• Represent QC and serve as a primary contact for manufacturing and other departments.
• Enter data into electronic systems and generate analytical reports.
• Initiate and perform laboratory investigations including document reviews and interviews.
• Assist with data trending, lab maintenance, and onboarding/training of new personnel.
• Develop, optimize, update SOPs and testing methods.
• Maintain compliance with cGMP, GLP and environmental safety guidelines.

Skills

cGMP practices

Teamwork

Communication

Education

Bachelor's degree in Biology/Microbiology/Biochemistry/Chemistry or related

AA with 4 years of related experience

Job description

The Position

As a QC Analyst II in our Quality department in Oceanside, you will play a critical role in ensuring the safety, quality, and compliance of our manufacturing environment and commercial products. You will collaborate closely with cross-functional teams using state-of-the-art techniques to implement innovative testing technologies. This role offers a unique opportunity to directly impact patient lives by maintaining the highest standards of good manufacturing and laboratory practices.

The Opportunity

• Conduct routine and non-routine analysis of the manufacturing environment and in-process commercial products according to standard operating procedures.
• Perform microbiological and chemical assays, basic troubleshooting, and equipment calibration and maintenance.
• Represent QC and serve as a primary point of contact for manufacturing and other operational departments.
• Collect, process, and enter data into electronic systems to generate accurate analytical reports.
• Initiate, compile, and perform laboratory investigations, including document reviews, interviews, and tracking.
• Assist with data trending, data review, lab maintenance, and the onboarding and training of new personnel.
• Develop, optimize, revise, and update standard operating procedures and testing methods.
• Maintain compliance with cGMP, GLP, and environmental safety guidelines to foster a positive safety culture.

Who you are

• You hold a Bachelor's Degree in Biology, Microbiology, Biochemistry, Chemistry, or a related discipline with 1 year of relevant experience (or an AA with 4 years, or HS diploma with 6 years of related experience).
• You are proficient in cGMP practices across all laboratory assignments and environments.
• You excel at teamwork, sharing responsibilities to accomplish required QC sample testing efficiently.
• You are able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA) for warehouse access.

Preferred

• You have experience utilizing state-of-the-art laboratory techniques and driving new technology implementations.
• You possess strong communication skills and experience participating in routine cross-departmental projects and investigations.

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.