New · posted Nov 4
Genentech · Biotechnology
Quality Control Analyst II - Fixed Term
- Oceanside, CA
- On-site
- Full-time
- Associate & Specialist
The role
- 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.
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.
What you need
- 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.
Preferrednice to have
- 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
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.
Pay and benefits
$45,200 – $83,900 a year
Employer providedDiscretionary annual bonus
Where you'll work
Oceanside, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in Oceanside, CAEqual opportunity, accessibility and legal noticesGenentech's statements, word for word
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.
Job intelligence
The context around this role
Live data · November 4, 2026
Salary intelligence
How the pay compares
This role's midpoint is 12% below the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in California9 roles publishing pay
Associate & Specialist roles in the US79 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $45,200 | — | $83,900 |
| California (middle half) | $58,500 | $64,500 | $77,000 |
| All US (middle half) | $59,250 | $73,000 | $88,250 |
This role: Genentech's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, November 4, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 242 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Genentech's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods12
- GMP and compliance3
- Collaboration and leadership3
- Documentation and SOPs2
- Data and digital systems2
- Clinical trial conduct2
- Investigations and CAPA1
- Validation and qualification1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Control work in biotechnology, led by the four this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticalsNamed in the posting
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and AnswersNamed in the posting
- FDA21 CFR Part 58 (GLP)(official source, opens in a new tab)Good laboratory practice for nonclinical laboratory studiesNamed in the posting
- EUEU Good Distribution Practice(official source, opens in a new tab)Guidelines on good distribution practice of medicinal products for human useNamed in the posting
- USPUSP–NF(official source, opens in a new tab)US Pharmacopeia general chapters and monographs, such as <61> bioburden, <85> endotoxin, <1225> validation
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
- ISPEISPE GAMP 5(official source, opens in a new tab)A risk-based approach to compliant GxP computerized systems
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- ICHICH Q2(R2) and Q14(official source, opens in a new tab)Validation and development of analytical procedures
- FDAFDA analytical procedures guidance(official source, opens in a new tab)Analytical Procedures and Methods Validation for Drugs and Biologics
- ICHICH Q1 stability testing(official source, opens in a new tab)Stability testing of drug substances and drug products
- EDQMEuropean Pharmacopoeia(official source, opens in a new tab)The Ph. Eur. quality standards for medicines in Europe, published by the EDQM
- ICHICH Q3 impurities(official source, opens in a new tab)Impurities in drug substances and products, residual solvents and elemental impurities
- FDAFDA aseptic processing guidance(official source, opens in a new tab)Sterile Drug Products Produced by Aseptic Processing: Current Good Manufacturing Practice
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- EUEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules, including Annex 1 sterile and Annex 15 validation
Company hiring pulse
Genentech on Regulatory Jobs
- 26
- Open roles
- 25
- Distinct roles
- 6
- Locations
By discipline
- Quality15 58%
- Regulatory7 27%
- Clinical4 15%
By level
- Senior & Principal19 73%
- Director3 12%
- VP & Executive2 8%
More roles at Genentech
- View role
Senior Manager, QC Chemistry and Device Testing (CVRM)
Holly Springs, NCManagerPharmaceuticals$120K–$223K
- View role
Quality Site Head
Oceanside, CAVP & ExecutiveBiotechnology$201K–$374K
- View role
Senior Pharmacovigilance (PV) Clinical Scientist
South San Francisco, CASenior & PrincipalBiotechnologySalary not listed
- View role
Clinical Research Engagement Lead - Northeast Region
Cincinnati, OHSenior & PrincipalBiotechnology$103K–$192K
Similar Quality Control roles elsewhere
- View role
Analyst I, QC - Swing Shift
LGC GroupPetaluma, CAAssociate & SpecialistBiotechnology$52K–$73K
- View role
Quality Controls Lab Operations Specialist (Overnights)
RegeneronSaratoga Springs, NYAssociate & SpecialistBiotechnology$62K–$131K
- View role
Quality Control Operations Specialist
RegeneronSaratoga Springs, NYAssociate & SpecialistBiotechnology$62K–$131K
- View role
Quality Control Operations Specialist (Overnights)
RegeneronSaratoga Springs, NYAssociate & SpecialistBiotechnology$62K–$131K
Quality Control Analyst II - Fixed Term at Genentech
Applications close November 9. $45K–$84K a year, employer provided.