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

Valspec

Process Validation Engineer

Oceanside, CA

$70 - $80/hr

Process Engineer -- Upstream / Downstream / Clean Utilities (Consultant) -- Contract Engagement ... biotech GMP manufacturing environment. * Hands-on experience in at least one of: Upstream (cell ...

Dover Corporation

Product Design Engineer

Grand Terrace, CA · On-site

$127K - $153K/yr

... Biotech, Quantex™, Quattroflow ® , and Wilden ® . PSG products are manufactured on three ... 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 Aug 1, 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 engineers make $300,000 a year?

Senior biotech process engineers with extensive experience, advanced skills in bioprocessing, and leadership roles can earn $300,000 or more annually. High compensation is often associated with working in specialized areas, managing large-scale production, or holding executive-level responsibilities in the biotech industry.

What is process engineering in biotechnology?

Process engineering in biotechnology involves designing, developing, and optimizing manufacturing processes for biological products such as pharmaceuticals, vaccines, and biofuels. Biotech process engineers work with equipment like bioreactors and use techniques such as fermentation and purification to ensure efficient, scalable, and compliant production. They often require knowledge of chemical engineering principles, laboratory skills, and familiarity with regulatory standards.

What engineers make $500,000?

Senior biotech process engineers with extensive experience, advanced skills in bioprocessing, and leadership roles can earn salaries approaching or exceeding $500,000, especially in high-cost-of-living areas or with bonuses and stock options. Such compensation typically requires a combination of technical expertise, management responsibilities, and industry demand.

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 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 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 engineers make $200,000 a year?

Biotech process engineers can earn $200,000 or more annually, especially with extensive experience, advanced degrees, or leadership roles in the industry. High salaries are often associated with senior positions, specialized skills in bioprocessing, and working in competitive biotech or pharmaceutical companies.

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 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 July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $97,362 per year, or $46.8 per hour.

Process Validation Engineer

Valspec

Oceanside, CA

$70 - $80/hr

Full-time, Contractor

Posted 11 days ago

Job description

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.

Valspec's projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.

Process Engineer — Upstream / Downstream / Clean Utilities (Consultant) — Contract

Engagement: Valspec consultant placed onsite at a major biopharmaceutical manufacturing site in the Raleigh-Durham, NC area

Location: Raleigh-Durham, NC (onsite)

Type: Contract / consulting — initial term approximately 12 months, with a possibility of extension

Start: ASAP

About the Engagement

Valspec is seeking Process Engineers to support large-scale biologics drug substance manufacturing at a major biopharmaceutical site in the Raleigh-Durham area. We're looking for candidates who can step into an active, fast-moving environment and contribute with minimal ramp-up. Openings across Upstream, Downstream, and Clean Utilities — candidates with a strength in one area are encouraged to apply.

Role Overview

The Process Engineer will provide engineering support to production and startup activities across Drug Substance manufacturing, with a primary focus in one of the following areas depending on team assignment: Upstream (cell culture/bioreactors), Downstream (purification/chromatography), or Clean Utilities (WFI, clean steam, process gases, and supporting utility systems). This person will partner closely with Manufacturing, Manufacturing Sciences (MSAT), Automation, and Quality to troubleshoot process issues and support equipment and process reliability.

Key Responsibilities
  • Provide engineering technical support for assigned process area, specifying equipment and process gaps within existing facility design.
  • Troubleshoot production and startup issues, partnering with Manufacturing and Maintenance to minimize downtime and support equipment reliability.
  • Support process monitoring and control activities within the assigned functional area, ensuring compliance with cGMP requirements.
  • Author and review technical documentation, including SOPs, protocols, deviations, and change controls, within GMP quality systems.
  • Support process characterization, technology transfer, and continuous improvement initiatives.
Required Qualifications
  • BS in Chemical, Biochemical, Mechanical, or Biomedical Engineering, or a related technical field.
  • 5+ years of process or manufacturing engineering experience in a pharmaceutical or biotech GMP manufacturing environment.
  • Hands-on experience in at least one of: Upstream (cell culture/bioreactor) operations, Downstream (purification) operations, or Clean Utilities systems.
  • Working knowledge of cGMP requirements in a regulated biologics manufacturing environment.
  • Able to work onsite in the Raleigh-Durham, NC area and be fully productive quickly given the engagement timeline.
Preferred Qualifications
  • Large-scale biologics drug substance experience (mammalian cell culture and downstream purification).
  • Experience supporting a startup, commissioning, or new-facility environment.
  • Familiarity with relevant unit operations depending on focus area: bioreactors and cell culture systems (Upstream); chromatography, UF/DF, and viral filtration (Downstream); or WFI, clean steam, and process gas systems (Clean Utilities).
Join Us

Salary Range: $70 - $80 / hourly range is an estimate of pay for project-based employment. Range varies based on knowledge, experience, and area of focus. Higher rates possible for short-term assignments and independent contractors. Apply now to be part of a dynamic team driving innovation in North Carolina and beyond.

Why Join Valspec?

At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation. We also offer a highly competitive benefits package, including:

  • Premium medical coverage
  • 401(k) with company match
  • Tuition reimbursement
  • Unique performance incentives
  • And more — all designed to support your growth, well-being, and future.

Join a team where your contributions matter, your development is prioritized, and your success is shared.

When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net or @valspec.net. Any other domains are impersonations and should be ignored.

Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time.

Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.

Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.