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Biotechnology Engineer Jobs in California (NOW HIRING)

Benchling

Agentic AI Engineer

San Francisco, CA · On-site

$176K - $265K/yr

We are rebuilding biotech for the AI era. When a breakthrough is delayed, the world waits. Getting ... Benchling is building Intelligence Engineering & Enablement, a small autonomous team within our ...

MNF Global

Biotech Patent Agent

Los Angeles, CA

$200K - $240K/yr

The successful candidate will work with innovative biotechnology companies, pharmaceutical organizations, diagnostics developers, and research institutions protecting breakthrough technologies across ...

JKI

Project Engineer

Walnut Creek, CA · On-site

JKI serves industries such as aerospace, automotive, energy, biotech, and semiconductors. JKI helps ... We are known for rapid iteration, LabVIEW software engineering best practices, FPGA and real-time ...

Debut Biotech

Staff Process Engineer

San Diego, CA · On-site

Our hybrid biotechnology approaches unlock latent markets, providing access to sustainably produced ... Staff Process Engineer Summary The Staff Process Engineer, Downstream Processing (DSP) will take a ...

JKI

Project Engineer

Walnut Creek, CA · On-site

JKI serves industries such as aerospace, automotive, energy, biotech, and semiconductors. JKI helps ... We are known for rapid iteration, LabVIEW software engineering best practices, FPGA and real-time ...

Amgen, Inc.

Sr Engineer

Thousand Oaks, CA · On-site

$109K - $150K/yr

Career Category Engineering Join Amgen's Mission of Serving Patients At Amgen, if you feel like you ... Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ...

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Biotechnology Engineer information

What does a biotechnology engineer do?

A Biotechnology Engineer applies principles of biology, chemistry, and engineering to develop products and technologies that improve human health, agriculture, and the environment. Their work includes designing processes for producing medicines, biofuels, and food, as well as developing equipment and systems for biotechnology applications. Biotechnology Engineers often collaborate with scientists and other engineers to innovate and solve complex biological problems, making their role crucial in advancing medical and agricultural technologies.

What are the key skills and qualifications needed to thrive as a biotechnology engineer?

To thrive as a Biotechnology Engineer, you need a strong background in biology, chemistry, and engineering principles, typically supported by a bachelor's or master's degree in biotechnology or a related field. Familiarity with laboratory equipment, bioinformatics tools, and regulatory standards such as GMP is essential. Critical thinking, problem-solving, and effective teamwork are standout soft skills in this role. These skills and qualities are crucial for developing innovative solutions and ensuring compliance in the rapidly evolving biotechnology industry.

What is the difference between Biotechnology Engineer vs Biomedical Engineer?

AspectBiotechnology EngineerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biotechnology, Bioengineering, or related fieldsBachelor's or Master's in Biomedical Engineering, Bioengineering, or related fields
Work EnvironmentLaboratories, biotech companies, research facilitiesHospitals, medical device companies, research labs
Industry UsageBiotech firms, pharmaceutical companies, agricultural biotech
Common Search IntentComparing roles in biotech development and research

Biotechnology Engineers focus on developing and improving biotechnological products, often working in labs and biotech firms. Biomedical Engineers design medical devices and work closely with healthcare providers. While both roles require similar educational backgrounds, their work environments and industry applications differ, catering to different aspects of the life sciences sector.

What are some common challenges biotechnology engineers face when working on interdisciplinary teams?

Biotechnology Engineers often collaborate with professionals from biology, chemistry, computer science, and engineering backgrounds. A common challenge is bridging communication gaps due to varying technical vocabularies and priorities among disciplines. Successful engineers develop strong teamwork and communication skills to align goals, understand constraints, and integrate diverse expertise into innovative solutions. Building mutual respect and fostering open dialogue are essential for effective interdisciplinary collaboration.
What are popular job titles related to Biotechnology Engineer jobs in California? For Biotechnology Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Biotechnology Engineer jobs in California look for? The top searched job categories for Biotechnology Engineer jobs in California are:
What cities in California are hiring for Biotechnology Engineer jobs? Cities in California with the most Biotechnology Engineer job openings:
Biotechnology Engineer jobs near you
Infographic showing various Biotechnology Engineer job openings in California as of August 2026, with employment types broken down into 77% Full Time, 5% Part Time, and 18% Contract. Highlights an 90% In-person, and 10% Remote job distribution.

PHARMACEUTICAL - SR. CQV ENGINEER

MMR Consulting

Irvine, CA • On-site

Other

Re-posted 3 days ago

Job description

Previous Pharmaceutical/Biotech experience is mandatory for this role
MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering, Project Management, and Validation.
MMR Consulting has offices in Canada, USA, and Australia.
This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of engineers involved in the design, commissioning & qualification, start-up and project management of various processes, systems, and facilities. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.
This role is for Sr. CQV Engineer will require to work on the validation of upstream and downstream bioprocess systems/equipment in the biopharmaceutical industry, as well as process equipment in pharma/biotech industries. The ideal candidate should possess leadership skills to lead teams of intermediate & junior engineers.
The work will require working out of client's facilities, which are typically in Irvine, California & surrounding areas.
Responsibilities
  • Provide technical guidance in the commissioning, qualification and start-up of various pharmaceutical / biopharmaceutical cGMP process equipment, utilities & facilities.
  • Lead the development (for example, write test cases) of key qualification deliverables such as DQ, FAT, SAT, IQ, OQ and PQ during the project lifecycle.
  • Able to perform field execution of qualification test cases and protocols.
  • Support development of Project Validation Plans (PVPs) to ensure the action plan to test the system is applicable and relevant.
  • Lead qualification processes throughout the project lifecycle to ensure timely completion and to ensure all quality and engineering specifications are met.
  • Possess knowledge of relevant regulatory requirements and industry best practices on all or any of the following - Process equipment, clean utilities, automation systems, laboratory equipment, building & facilities
  • Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, and provide updates.
  • Engage other departments, as required, in the design reviews and decisions.
  • Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
  • Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification, and validation phases.
  • Visit construction and installation sites, wearing necessary safety PPE.
  • You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
  • Supervise contractors during critical testing of system and equipment.
  • Other duties as assigned by client, and/or MMR, based on workload and project requirements.
  • As this position requires working on client sites, you will need to comply with the client's safety rules including mandatory vaccination policies for COVID-19, where applicable
  • Lead/Mentor a team of validation engineers/specialists.

Qualifications
  • 12+ years of experience in commissioning, qualification or validation of various systems within the pharmaceutical/biotech industry.
  • Previous experience in the pharmaceutical / biotech industry, with knowledge of requirements for cGMP operations.
  • Validation experience such as cleaning validation, thermal validation, mixing studies, process validation, computer systems validation is an asset but not required.
  • Experience with developing and executing validation projects to Risk-Based Commissioning & Qualification approaches, such as ASTM E-2500 or ISPE ICQ, is considered an asset, but not required.
  • Experience with commissioning & qualification of process control systems (i.e. PCS, SCADA, Historians) and building automation systems are considered an asset.
  • Experience with commissioning and qualifications of biotech process equipment, such as some, but not all, of the following: fermentation, bioreactors, downstream purification processes (chromatography, TFF, UF), CIP systems, Buffer systems, Clean Utilities would be an asset.
  • Experience with Qualification or Validation of clean utilities and ISO clean rooms.
  • Experience with preparation and execution of URS's, DQ's, RTMs, Risk Assessments, CPPs, VPPs, FATs, SATs, IOQs
  • Lead teams of Validation staff, manage staff priorities, provide mentorship/oversight, help staff resolve issues. Leadership is considered an asset but not required.
  • Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexities.
  • Possess mentorship skills, to coach and develop junior and intermediate employees.
  • Engineering degree, preferably in Mechanical, Electrical or Chemical.
  • Travel may be required on occasion.
  • Ability to handle multiple projects and work in a fast-paced environment.
  • Strong multi-tasking skills
  • Ability to lift 50 lbs.

Compensation: 100,000$ - 115,000$ based on experience.
Equal Employment Opportunity and Reasonable Accommodations
MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.

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