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Genentech Contractor Jobs (NOW HIRING)

... Genentech is seeking a talented and enthusiastic candidate for a full-time lab-based Scientist II contractor position. The ACE Hub is an interdisciplinary team with a mission to accelerate drug ...

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How much do genentech contractor jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for genentech contractor in the United States is $37.61, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $37.26 per hour, depending on experience, location, and employer.

What does a Genentech contractor do?

As a Genentech Contractor, you may be assigned to projects such as process improvements, regulatory documentation, research support, or quality assurance initiatives, depending on your area of expertise. Contractors typically collaborate closely with full-time staff and other teams to ensure projects are completed efficiently, within compliance standards, and to high-quality benchmarks. You'll likely attend team meetings, contribute to project planning, and be responsible for delivering results within set timelines. Your contributions are crucial in helping Genentech maintain its reputation for innovation, efficiency, and compliance in the biotechnology industry.

What is a Genentech contractor?

A Genentech Contractor is a professional hired on a temporary or contract basis to work at Genentech, a biotechnology company. Contractors may work in various departments, including research, manufacturing, IT, or administration, depending on their expertise. Unlike full-time employees, contractors are typically employed by a third-party staffing agency and may not receive the same benefits. However, contracting can provide valuable industry experience and potential opportunities for full-time roles.

What are the key skills and qualifications needed to thrive as a Genentech contractor?

To thrive as a Genentech Contractor, you need relevant industry experience, a strong understanding of biotechnology processes, and academic credentials suited to your specialization (such as life sciences, quality assurance, or engineering). Familiarity with industry-standard tools such as Good Manufacturing Practices (GMP), electronic document management systems, and possibly certifications like Six Sigma or Lean are often required. Strong communication, adaptability, and collaborative problem-solving skills help you integrate quickly within cross-functional teams. These skills and qualities ensure project success, regulatory compliance, and effective teamwork in a dynamic and innovative pharmaceutical environment.

More about Genentech Contractor jobs
What cities are hiring for Genentech Contractor jobs? Cities with the most Genentech Contractor job openings:
What states have the most Genentech Contractor jobs? States with the most job openings for Genentech Contractor jobs include:
What job categories do people searching Genentech Contractor jobs look for? The top searched job categories for Genentech Contractor jobs are:
Infographic showing various Genentech Contractor job openings in the United States as of August 2026, with employment types broken down into 70% Full Time, 9% Part Time, and 21% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $78,225 per year, or $37.6 per hour.

Principal Project Engineer for Single-Use Equipment

Genentech, Inc.

Oceanside, CA • On-site

$109K - $204K/yr

Full-time

Re-posted 23 days ago


Genentech rating

8.8

Company rating: 8.8 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical


Job description

This role is a key part of our Equipment Engineering team, dedicated to delivering cutting-edge solutions for Single-use Systems in biologics manufacturing. As a member of this team, you will play a pivotal role in managing complex projects, collaborating with multidisciplinary teams, and ensuring compliance with industry and regulatory standards. This position offers the opportunity to work with global stakeholders, mentor engineers, and contribute to the advancement of innovative technologies that support our mission of delivering high-quality, life-saving medicines to patients worldwide.
The Opportunity
As a Principal Project Engineer for Single-Use Equipment, you will serve as a technical leader responsible for managing and delivering engineering projects focused on biologics process equipment, ensuring compliance with industry standards, regulatory requirements, and Roche guidelines. You will drive collaboration across disciplines and global stakeholders to achieve project goals while implementing innovative solutions for GMP-compliant manufacturing systems. Additionally, you will:
  • Lead the planning, design, and execution of engineering projects for single-use biologics process equipment.
  • Manage sub-project budgets, schedules, resources, and risks to ensure timely and cost-effective project delivery.
  • Serve as the primary interface with equipment suppliers for technical specifications, design reviews, and performance validation.
  • Oversee Factory Acceptance Tests, Site Acceptance Tests, and equipment qualification activities, ensuring systems meet GMP compliance.
  • Develop and manage relationships with external vendors and contractors to ensure quality execution and timely delivery of project scope.
  • Provide mentoring and technical guidance to less experienced engineers to foster professional growth and team excellence.
  • Drive alignment with key stakeholders, ensuring consistent communication and decision-making throughout project phases.

Who You Are
  • Bachelor's Degree in Chemical Engineering, Mechanical Engineering, or related discipline with 8+ years of experience preferably in pharmaceutical biologics molecule drug substance equipment, 6+ years of experience with a Master's Degree.
  • Experience managing international capital projects related to biologics molecule drug substance equipment, with typical project budgets ranging from 15 to 50m CHF.
  • Operational experience with biologics systems (bioreactors, chromatography skids, filtration systems, centrifuges, laminar flow hoods, etc.).
  • Experience with equipment manufacturer collaboration, FAT/SAT execution, and equipment commissioning/qualification activities.
  • Demonstrated ability to execute highly complex scope on mid-sized to large-scale projects.
  • Experience with regulatory compliance (FDA, EMA) and GMP requirements for biologics manufacturing operations.
  • Project delivery experience in pharmaceutical manufacturing environments.
  • Significant travel (50-60%) assignment requiring weekly commuting and/or temporary remote assignment as required to meet the business need (including on-site presence during FAT/SAT activities). International project assignment of 1 to 3 years as required to meet the business need.

Preferred:
  • MS in Engineering (Chemical or Mechanical) and/or an MBA

This is an on-site position; no remote options are available at this time.
Relocation benefits are not available for this posting.
The expected salary range for this position based on the primary location of California is $109,900 - $204,100 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 in this link.
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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About Genentech

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A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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