Bioprocess Technician - Clinical Supply Center

Genentech

San Francisco (CA)

On-site

USD 61,000 - 128,000

Full time

5 days ago
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Job summary

Genentech’s Bioprocess Technician role sits within the Clinical Supply Center (DS Manufacturing) in South San Francisco. You will work on end-to-end operations from Solution Preparation to Downstream, aligning with GMP, Lean/Agile, and collaboration-focused behaviors to deliver quality products.

We seek a candidate with a life-science background, experience with single-use technology, and a proven ability to problem-solve in a dynamic, team-driven environment.

Qualifications

  • BA/BS in life science or engineering; 3+ years of relevant work experience in GMP manufacturing.
  • Experience with single-use technology.
  • Able to work in a fast-paced, ambiguous environment.
  • Strong collaboration and problem-solving in cross-functional teams.

Responsibilities

  • Ensure operation activities are executed on time and per procedures.
  • Drive continuous improvement in our process to gain efficiency.
  • Collaborate proactively with peers and support groups (Automation, Quality, Vendor, Facility).
  • Understand Drug Substance process parameters and recognize issues.
  • Escalate Basecamp recipe issues and ensure timely resolution.
  • Facilitate communication and information transfer between groups.

Skills

Collaboration
Problem solving
Customer service
Agile mindset

Education

BA/BS in life science or engineering

Tools

ASPIRE/SAP
Syncade
DeltaV
MES
LIMS

Job description

The Position

The Bioprocess Technician is a member of the Operations, Process Support and Process Engineering (OPP) team for the Clinical Supply Center (CSC) Drug Substance (DS) Manufacturing in South San Francisco (SSF).

The Bioprocess Technician will be comfortable with ambiguity, have an entrepreneurial spirit within a GMP environment, have demonstrated strong Pharma Technical Behaviors,and have an agile mindset. Ability to collaborate is crucial as success will be measured as a member of a team, not just as an individual.

In this role the Bioprocess Technician will be part of the CSC Main Operation team that executes all operation activities on the production schedule. The candidate will establish relationships with customer groups and peers by seeking opportunities for collaboration, proactively communicating and become proficient on the end to end process from Solution Preparation to Downstream. Candidates are initially expected to have a fundamental understanding of the cell culture and purification process and will develop additional expertise over time through a combination of role assignments and coaching.

This position requires an on-site presence in order to perform the essential operation activities and operational responsibilities of the role.

Monday to Friday day shift

NOTE- Weekend work, off hours and swing shift work may be required

The Opportunity
  • Accountable for ensuring that production timelines are met
  • Perform a variety of tasks to ensure that all the materials, recipes and consumables are available when needed. (e.g. ASPIRE/ SAP, 5S)
  • Execute main operation activities associated with Upstream and Downstream operations (e.g. inoculation, batch and prep, harvest, chromatography, viral filtration). Will also support Solution Prep activities as needed.
  • Perform routine EM and WFI sampling and EMS verification.
  • Perform accurate real-time documentation on all required worksheets and software.
  • Proactive communication with management, researchers and peers to provide feedback on operations.
  • Operation and understanding of automation/process systems. (e.g. Syncade, DeltaV, MES, Single LIMS)
  • Exercise good independent judgment and provide potential solutions to problems based on experience with GLP, cGMP, QMS, Lean Manufacturing principles.
  • Ability to work with minimal supervision.
  • Strong behaviors aligned with Pharma Technical (PT) expectations including Lean/Agile, collaboration, speaking up, decision making and continuous improvement
  • Ability to work in an agile and ambiguous environment
  • Commitment to quality and excellence
  • Growth mindset with a passion for taking on challenges in order to deliver business value while developing
  • Entrepreneurial spirit within a GMP environment
Operational Responsibilities
  • To ensure operation activities are executed on time and according to procedures.
  • Drives continuous improvement in our process to gain efficiency.
  • Collaborates proactively with peers and support groups (e.g. Automation, Quality, Vendor, and Facility) to ensure robust communication.
  • Understands Drug Substance process parameters and is able to recognize when there is an issue.
  • Escalate Basecamp recipe issues and ensure they are being addressed in a timely manner.
  • Facilitates communication and information transfer between different groups.
Who You Are
  • BA/BS in a life science, engineering or equivalent is preferred with at least three years of relevant work experience
  • Ability to work in fast paced dynamic work environment
  • Experience using single use technology
  • Ability to prioritize project assignments, to meet deadlines, be flexible in workload priorities, and to recognize and accurately report problems
  • Proven excellent in customer service and ability to problem-solve and make decisions
  • Working conditions include extensive walking/standing, ability to lift, push and pull up to 30 pounds
  • Be able to work a flexible schedule (e.g Day, Weekend and Swing Shift Schedule)

Relocation benefits are not available for this position.

The expected salary range for this position based on the primary location of California is $61,300 to $113,900 for MT3 and $68,740 to $127,660 for MT4. 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.

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