Quality Control Associate

Genentech • Oceanside, CA

1d • Hybrid

About The Position

At Genentech, we are passionate about improving patients' lives and creating healthier communities for all. We foster a culture of inclusivity, integrity, and creativity while boldly pursuing answers to the world's most complex problems. We believe diversity and inclusion drives innovation and contributes to equitable healthcare access for all. At Genentech, different backgrounds and perspectives are essential. We believe every employee makes a difference. The focus of Oceanside Operations is Drug Substance bulk manufacturing. We have a passion for science, technology, innovation, professional development, and diversity and inclusion. Our vision is to have a greater overall impact and benefit to the patient. We hope you consider joining our team and being part of one of the best biotechnology facilities in the world. The Opportunity Genentech is looking for a Quality Control Associate I in Oceanside, California. This position is primarily responsible for compendial method testing, Bulk Drug Substance testing, reagent preparation, and sample management for biopharmaceutical products. Additional responsibilities include equipment management and maintenance, and laboratory duties.

Requirements

• Bachelor’s degree in Chemistry, Biochemistry, or a related scientific discipline
• 3-4 years of experience in pharmaceutical/biotech QC labs
• Basic knowledge in Chromatography and chemical testing assays
• Basic equipment troubleshooting techniques
• Proficiency in all necessary wet chemistry methods
• Experience working in a GMP environment
• Ability to read and follow Standard Operating Procedures precisely
• Knowledge of laboratory safety procedures
• Basic experience supporting quality events
• Proficiency with laboratory electronic systems, including LIMS and Microsoft Office
• Excellent organizational skills
• Ability to be agile and work independently in a fast-paced environment
• Experience working on group projects
• Proficient in time management with oversight
• Excellent interpersonal, written, and verbal communication skills
• Continuous improvement mindset
• Basic experience supporting audit or inspection activities
• Must be able to stand, walk, and use laboratory equipment for extended periods
• Ability to lift up to 35 lbs
• Wear necessary personal protective equipment (PPE)

Nice To Haves

• Working knowledge of Empower or GSMP software is preferred
• Familiarity with tech transfer activities
• Familiarity with auditing processes
• Attending meetings, seminars, or classes to support organizational goals

Responsibilities

• Compendial method testing
• Bulk Drug Substance testing
• Reagent preparation
• Sample management for biopharmaceutical products
• Equipment management and maintenance
• Laboratory duties

Benefits

• Relocation benefits are available
• A discretionary annual bonus may be available based on individual and Company performance

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees