Manufacturing Associate Technician

GenentechGenentechSan Diego County, California, United States
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Posted

9/18/2026

Employment

Full time

Range

$43k - $80k/year

Work style

On-site

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AI summary

Core responsibilities

Operate and monitor automated biomanufacturing systems to produce biotherapeutic medicines while maintaining strict cGMP and safety standards. Perform core processes such as cell culture, protein purification, and media preparation while ensuring accurate documentation of all activities.

Requirements overview

Requires a High School Diploma or equivalent and experience in bioprocessing or biopharmaceutical technology. Candidates must be comfortable working in a physically demanding cleanroom environment and possess strong communication and documentation skills.

Key skills

BioprocessingCell cultureProtein purificationcGMPSOP complianceAutomated production systemsAnalytical toolsMedia preparationBuffer preparationCleanroom maintenanceDocumentationTroubleshootingSafety complianceBiopharmaceutical technologyColumn chromatographyCIP/SIP

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Education requirements

high schoolprofessional certificate

About Genentech

Industry

Biotechnology Research

Employees

18,211

Type

Privately Held

Size

10,001+ employees

About Genentech We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal. Making a difference in the lives of millions starts when you make a change in yours. If you’d like to join our team, view our openings at gene.com/careers. Our patient resource center is dedicated to getting patients and caregivers to the right resources. You can reach them at 1 (877) GENENTECH (436-3683) Monday-Friday, 6am-5pm PST or patientinfo@gene.com. Community Guidelines: 1. We want to foster positive conversation around the issues we are passionate about. To that end, we remove profanity, content that contains threatening language, content that is aimed at private individuals, personal information, and repeated unwanted messages. 2. Don’t mention any medicines by name — ours or anyone else’s. Because of the fair balance rules governing our industry, we cannot post any comments that reference any pharmaceutical brand, product, or service. Please do not mention any specific medicines by name, or include any links to third party sites in your comments. 3. This isn’t the place to report or discuss side effects. This site is not intended as a forum for reporting side effects experienced while taking a Genentech product. Instead, you should report any side effects to Genentech Drug Safety at 1-888-835-2555. You can also report side effects of any prescription product directly to the FDA at 1-800-FDA-1088 or by visiting www.FDA.gov/medwatch. 4. Don’t pitch your product or service. Please don't use our page as a place to promote your product or pitch your services. Please also avoid posting links to external sites. We reserve the right to remove any posts that are deemed promotional.

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Job categories

ManufacturingHealthcareScience & ResearchEngineering

Description

The Position 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. As a Bioprocess Technician, you will join our dynamic cGMP manufacturing team, directly impacting patient lives by producing innovative biotherapeutic medicines using state-of-the-art automated systems. Operating across cell culture, purification, or manufacturing services, you play a vital role in maintaining the highest standards of safety, quality, and inspection preparedness. The Opportunity: Operate, monitor, and troubleshoot automated production systems, cleaning/sterilization equipment, and benchtop analytical tools. Perform core biomanufacturing activities, including cell culture growth, sampling, harvesting, protein purification, formulation, freeze-thaw, and transfer processes. Prepare essential media and buffer solutions according to precise production guidelines. Maintain cleanroom environments, fixed tank systems, and filtration units in strict compliance with cGMP, SOP, and safety standards. Perform detail-oriented documentation by accurately reviewing process tickets, equipment readings, and calculations. Collaborate closely with cross-functional team members and supervisors to quickly resolve minor equipment and operational deviations. Foster a positive, proactive safety culture by immediately reporting incidents, near misses, and environmental concerns. Who you are: You hold a High School Diploma or equivalent qualification. You bring background knowledge or experience in bio-processing and biopharmaceutical technology. You possess strong oral and written communication skills with the ability to document process information accurately. You are comfortable using computer-based systems and operating automated equipment. You thrive in a physically active cleanroom environment, which includes standing for 8–10 hours, climbing stairs, lifting up to 30 lbs, and adhering to strict gowning requirements (e.g., scrubs, bunny suits, steel-toe boots). Preferred: A Biotech certificate from an approved program or 1–2 years of hands-on biopharmaceutical manufacturing experience. Demonstrated proficiency in at least one key manufacturing functional area (e.g., bioreactor operation, column chromatography, or automated CIP/SIP). Relocation benefits are not available for this posting The expected salary range for this position based on the primary location for this position of Oceanside, CA is $43,300.00 - $80,300.00 USD Annual. Actual pay will be determined based on experience, level, 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. 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.

Requirements

  • Bioprocessing
  • Cell culture
  • Protein purification
  • cGMP
  • SOP compliance
  • Automated production systems
  • Analytical tools
  • Media preparation
  • Buffer preparation
  • Cleanroom maintenance
  • Documentation
  • Troubleshooting
  • Safety compliance
  • Biopharmaceutical technology
  • Column chromatography
  • CIP/SIP

Benefits

  • Annual bonus

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