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Quality Site Head, Oceanside

Genentech · Oceanside, CA

Apply on Genentech ↗
Level
Specialist
Team
Quality
Base pay
$201k–$374k
Travel
20%
Degree
Required
Experience asked
15+ years
Industry
Pharma & life sciences
Posted
3 days ago

The role in 30 seconds

A specialist quality role at Genentech (pharma & life sciences) in Oceanside, CA.

They ask for
15+ years · degree required
Tools it names
Lean, Value stream mapping, FDA / GMP
Base pay
$201k–$374k
Day to day
about 20% travel

Read from the posting. The full description is below.

From the plant jobs report · week of November 2, 2026

Quality Engineer roles in California: typical posted base $100k–$153k. This one lists $201k–$374k.

Median of the low and high ends of 117 live postings that list pay, out of 227 quality engineer openings in California, read from manufacturers' own careers sites.

California plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 226 other live quality postings in California.

Base pay
About 131% above similar roles

Typical $100k–$149k, from 113 postings that list pay.

Experience asked
More than usual (15+ vs 5+)

Similar roles usually ask 5+ years.

Skills these teams ask for most

  • Root cause 75%
  • FMEA 49%
  • Supplier quality 44%
  • Validation (IQ/OQ/PQ) 42%
  • AS9100 41%
  • ISO 9001 35%

✓ = this posting asks for it too. % = share of similar postings that mention it.

Stands out: this posting asks for Value stream mapping, which few similar roles mention. If you have it, lead with it.

It asks for 15+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

At a glance

Promotion path mentioned

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Quality team at Genentech

    Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
    • How much of the job is customer complaints versus prevention?
    • The posting says about 20% travel. Between which sites?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

Full description from GenentechAs posted on their careers site.Show

Who you are

  • ✓You hold a Bachelor's degree in pharmaceutical, life sciences, physical sciences, or engineering with 15+ years of relevant bio/pharmaceutical experience in GMP regulated environments in Quality and preferably also manufacturing.
  • ✓You possess significant professional experience in Quality Assurance/Control, including cross-functional team management and leadership
  • ✓You have strong project management skills
  • ✓You have extensive professional experience with operations management in a facility that produces antibodies and biologics
  • ✓You have extensive knowledge of safety, quality systems and quality assurance concepts and systems, including the application of cGMPs.
  • ✓You have strong creative leadership skills, ability to build forward looking perspectives and remove barriers. Ability to inspire, adopt, coach and apply lean and agile ways of working. A consistent track record to perform against tight timelines in a highly complex and ambiguous environment. Expertise and experience in organizational change management and expertise in delivering a long-term vision is welcome
Show full description ↓

The Position

Pharma Technical Operations (PT) is responsible for managing all aspects of end-to-end drug substance and drug product manufacturing and supply. From the raw material to the final medicine, we contribute to deliver Roche’s ground-breaking therapies to more than 120 million patients around the world. We make our medicines at internal and external sites around the world and coordinate all aspects of production of Roche medicines in all disease areas and dosage forms.

This opportunity is located at Genentech’s Oceanside campus, a dedicated biologics drug substance manufacturing site specializing in commercial-scale production and rapid technology transfer. Utilizing dual stainless steel and state-of-the-art single-use manufacturing value streams, Oceanside plays a vital role in delivering life-saving therapies across Roche's commercial and clinical portfolio.

The Opportunity

As the Quality Site Head you are accountable for the design and qualification of our facility’s operations, including strategic workforce planning, hiring the respective personnel, setting up the organization, all relevant processes and documentation (e.g. SOPs). You are responsible for project management activities, IT systems and definition of the processes in compliance with GMP/Quality requirements. You will identify timeline risks or bottlenecks for the project or future site operations and take appropriate actions. You will work closely with all the key areas to achieve ambitious goals in terms of on time, on cost and on scope delivery.

You will work closely with the Site Head and other members of the Site Leadership team to shape excellence in operations and the strategy of the site. You are responsible for all Quality Operations affiliated with Quality Assurance and Quality Control business units for the Oceanside site and ensure that all processes and assets at the site are fully compliant with internal and external guidelines and regulations. You ensure effective use of resources and control of expenses to achieve maximum productivity; you develop and sustain robust scalable business processes and adjust and continuously improve them as needed. You are responsible for the achievement of complex and significant objectives through leadership and direction of significant multidimensional resources. You will build and maintain strong partnerships with the other departments on site within and beyond the Quality organisation to ensure site and department goals are achieved. You will also closely collaborate with other internal site Quality organisations and the global Quality organisation to support the network.

Involves travel up to 20%.

Your

include the following

  • •You will drive timely project execution through strategic thinking, technical and entrepreneurial understanding
  • •You will foster a strong mindset for safety, quality and compliance
  • •You will take purposeful and impactful decisions
  • •You will demonstrate disciplinary and professional leadership promotion and deployment of personnel including the assurance of adequate initial and ongoing training
  • •You will carry out employee appraisal reviews including performance assessment and salary responsibility
  • •You will define goals with employees and evaluate the achievement of goals. You will support the development of employees

Preferred

  • +You have an advanced degree (Masters or PhD)
  • +You have international experience at multiple sites/locations

This position also qualifies for the benefits detailed in this link .

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