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Biotech Process Engineer Jobs in Menifee, CA (NOW HIRING)

PM Group

CQV Engineer III

Oceanside, CA · On-site

$100K - $130K/yr

We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors ... Actively participant in the document approval process * Understanding of the entire validation life ...

Kite Pharma

Sr Validation Engineer I

Oceanside, CA · On-site

Serve as the KNEAT SME and power user, providing technical guidance, user support, process ... Master's degree with 5+yearsof experience in validation in a biotech/pharma industry * Experience ...

PM Group

CQV Engineer III

Oceanside, CA · On-site

$100K - $130K/yr

We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors ... Actively participant in the document approval process * Understanding of the entire validation life ...

Genentech

Principal Utilities Engineer

Oceanside, CA

$95K - $176K/yr

Partner with Process, Automation, Maintenance, and Quality teams to resolve complex technical ... biotech, pharmaceutical, or highly regulated cGMP facilities. Technical Expertise: * Hands-on ...

Abbott

Quality Engineer I

Temecula, CA · On-site

$35 - $40/hr

... on product quality,process compliance, investigation support, and continuous improvement ... Medical device, pharmaceutical, biotechnology, or other regulated manufacturing experience ...

Dover Corporation

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

Experience as an engineer in the pump industry is preferred * Minimum of 5 years of experience ... PSG is part of the Pumps & Process Solutions segment of Dover Corporation. For additional ...

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All JobsBiotech Process Engineer JobsBiotech Process Engineer Jobs in Menifee, CA

Biotech Process Engineer information

See Menifee, CA salary details

$52.4K

$97.4K

$150.8K

How much do biotech process engineer jobs pay per year?

As of Sep 6, 2026, the average yearly pay for biotech process engineer in Menifee, CA is $97,362.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,800.00 and $109,000.00 per year, depending on experience, location, and employer.

What does a Biotech Process Engineer do?

A Biotech Process Engineer designs, develops, and optimizes processes used in the production of biological products such as pharmaceuticals, vaccines, and biofuels. They work closely with scientists and manufacturing teams to scale up lab procedures to industrial levels while ensuring product quality and regulatory compliance. Their role often involves troubleshooting equipment, improving efficiency, and implementing new technologies within biotech manufacturing environments.

What are the key skills and qualifications needed to thrive as a Biotech Process Engineer, and why are they important?

To thrive as a Biotech Process Engineer, you need a solid background in chemical or biochemical engineering, process design, and regulatory compliance, typically supported by a relevant bachelor's or master's degree. Familiarity with process control systems, bioprocess simulation software, and industry-standard quality systems such as cGMP is essential. Strong analytical thinking, problem-solving abilities, and effective teamwork and communication skills help you excel in cross-functional environments. These skills ensure efficient, compliant, and innovative bioprocess operations, which are critical for product quality and organizational success.

What are some common challenges faced by Biotech Process Engineers during scale-up from laboratory to production?

Biotech Process Engineers often encounter challenges when scaling up processes from laboratory or pilot scale to full production. These challenges can include maintaining product consistency, ensuring process sterility, and adapting equipment to handle larger volumes without compromising yield or quality. Engineers must also collaborate closely with cross-functional teams such as quality assurance, validation, and manufacturing to implement changes efficiently and adhere to regulatory standards. Proactive problem-solving and strong communication skills are key to overcoming these hurdles and ensuring successful technology transfer.

What is the difference between Biotech Process Engineer vs Biotech Manufacturing Technician?

AspectBiotech Process EngineerBiotech Manufacturing Technician
CredentialsBachelor's degree in biotech, chemical engineering, or related field; often requires experience in process designAssociate's or bachelor's degree; focus on operational skills and equipment handling
Work EnvironmentDesigning, optimizing, and overseeing production processes in labs or manufacturing facilitiesOperating and maintaining equipment on the manufacturing floor
Job FocusProcess development, scale-up, troubleshooting, and process improvementExecuting production tasks, quality checks, and equipment setup

Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

What cities near Menifee, CA are hiring for Biotech Process Engineer jobs?

Cities near Menifee, CA with the most Biotech Process Engineer job openings:

Biotech Process Engineer jobs near you
Infographic showing various Biotech Process Engineer job openings in Menifee, CA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $97,362 per year, or $46.8 per hour.

Senior Project Engineer Process Automation

F. Hoffmann-La Roche AG

Oceanside, CA • On-site

$99.82 - $185.38/hr

Other

Posted 19 days ago

Job description

Role Overview

This Senior Project Engineer for Process Automation Systems will serve as a subject‑matter expert responsible for delivering advanced automation solutions for manufacturing, packaging, and warehouse operations across pharmaceutical and biotech environments.

The role entails ownership of the entire project lifecycle, ensuring compliance, performance, and successful execution while driving progress in digital manufacturing and Industry4.0 initiatives.

Key Responsibilities
  • Lead the planning, design, specification, procurement, implementation, and qualification of process automation systems, including DCS, PLC/SCADA, MES, and data historian platforms.
  • Define global automation architectures and system concepts, conducting feasibility studies and aligning solutions with Roche engineering standards.
  • Manage automation system integration with process equipment, utility systems, robotics, packaging & inspection systems, and warehouse automation.
  • Act as the technical and commercial interface to suppliers, integrators, engineering firms, and procurement teams, driving supplier innovation and performance.
  • Collaborate with multidisciplinary teams to align automation scope with project priorities and stakeholder expectations, providing regular progress updates and risk mitigation strategies.
  • Lead Computer System Validation (CSV), qualification activities, and commissioning efforts in compliance with GMP, FDA, EMA, and cybersecurity standards.
  • Support digital transformation initiatives through advanced process control, batch analytics, smart manufacturing, and IT/OT convergence solutions.
Qualifications
  • Bachelor’s degree in Automation Engineering, Mechatronics, or a related discipline (Master’s degree is a plus).
  • 5+ years of experience, preferably in the pharmaceutical or biotech industry.
  • Strong background in automation architecture design, project execution, commissioning and validation.
  • Demonstrated ability to execute complex scope on mid‑sized to large‑scale projects.
  • Experience with regulatory compliance (FDA, EMA) and GMP requirements for synthetic molecule manufacturing operations.
  • Project delivery experience in pharmaceutical manufacturing environments.
  • Significant travel (50% or more) with assignment required to meet business needs, including on‑site presence during FAT/SAT activities and international project assignments of 1 to 3 years.

Salary range based on the primary location of Oceanside: $99,820–$185,380. Compensation will be determined by experience, qualifications, geographic location, and other factors permitted by law. A discretionary annual bonus may be available.

Benefits are available in accordance with company policy. This is an on‑site position; no remote options are available at this time. Relocation benefits are not approved for this posting.

Genentech is an equal opportunity employer and prohibits unlawful discrimination. The company’s policy ensures a merit‑based employment process in compliance with federal, state, and local laws. Applicants requiring accommodations in the application process may contact the Accommodations for Applicants form.

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