Quality Control Analyst II - Fixed Term

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

Job summary

Genentech is seeking a Quality Control Analyst II in Oceanside to support biopharmaceutical product quality through routine testing, sample management, and lab maintenance. The role emphasizes data integrity, safety, and independent work in a fast-paced setting.

The position is a fixed duration for 2 years, with duties including routine testing, equipment maintenance, and adherence to GMP/GLP guidelines. A Bachelor’s degree in a relevant science and 0–2 years of experience are required.

Qualifications

• Bachelor’s degree in a related scientific discipline is required.
• 0–2 years of laboratory experience in a regulated environment.
• Strong organizational, time management, and problem-solving skills; able to work independently.
• Agile communicator with excellent interpersonal, written, and verbal skills.
• Working knowledge of laboratory safety protocols and software tools (LIMS, Microsoft Office, Google Workspace).

Responsibilities

• Perform routine compendial method testing (pH, osmolality, color) and chemical assays following SOPs and GMP guidelines.
• Conduct sample management, aliquoting, and reagent preparation to support routine testing operations.
• Oversee laboratory equipment through routine maintenance, calibration, and standardization.
• Execute basic troubleshooting of chemical assays and participate in special projects or protocol execution as needed.
• Maintain laboratory inventory, stock supplies, and keep the facility inspection-ready.
• Adhere to GMP, GLP, GDP, Data Integrity, and environmental safety guidelines.

Skills

Independent worker

Strong communication

Organizational skills

Problem-solving

Education

Bachelor’s Degree in Biology, Microbiology, Biochemistry, Chemistry, or related

Tools

LIMS

Microsoft Office

Google Workspace

Job description

The Position

We are seeking a Quality Control Analyst II to join our Quality team in Oceanside. In this role, you will play a crucial part in supporting biopharmaceutical product quality through routine testing, sample management, and laboratory maintenance. You will work independently in a fast-paced environment while upholding our commitment to data integrity and safety standards.

This is a fixed duration position for 2 years.

The Opportunity:

• Perform routine compendial method testing (pH, osmolality, color) and chemical assays following SOPs and GMP guidelines.
• Conduct sample management, aliquoting, and reagent preparation to support routine testing operations.
• Oversee laboratory equipment through routine maintenance, calibration, and standardization.
• Execute basic troubleshooting of chemical assays and participate in special projects or protocol execution as needed.
• Maintain laboratory inventory, stock supplies, and ensure the facility remains in an inspection-ready state.
• Adhere strictly to GMP, GLP, GDP, Data Integrity, and environmental safety guidelines.

Who you are:

• You hold a Bachelor's Degree in Biology, Microbiology, Biochemistry, Chemistry, or a related scientific discipline.
• You possess 0–2 years of related laboratory experience in a regulated environment.
• You demonstrate strong organizational, time management, and problem-solving skills with the ability to work independently.
• You are an agile communicator with excellent interpersonal, written, and verbal skills.
• You have working knowledge of laboratory safety protocols and software tools such as LIMS, Microsoft Office, and Google Workspace.

Work Environment/Physical Demands/Safety Considerations

• Work in office and laboratory environment.
• Able to stand, sit, and walk for extended periods of time.
• Able to lift up to 30lbs.
• Work with analytical instruments that may involve exposure to hazardous chemicals (corrosive, toxic, flammable, etc).
• Ability to perform repetitive tasks including frequent hand and finger manipulations, grasping pushing and pulling.
• Available to work over-time, weekends, and holidays as needed

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.