ZipRecruiter

Log In

1

Biotech Process Engineer Jobs in Los Angeles, CA

PM Group

Process Engineer

Irvine, CA

$100K - $130K/yr

Overview The Process Engineer position is an exciting opportunity to join PM Group's quickly ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

PM Group

Process Engineer

Irvine, CA · On-site

$100K - $130K/yr

Overview The Process Engineer position is an exciting opportunity to join PM Group's quickly ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

20BLOC

Process Scientist/Engineer

Thousand Oaks, CA · On-site

$90K/yr

We are looking for a motivated, hands-on Process Scientist/Engineer to join our team. This person ... Minimum 4 years' experience in bioprocessing environments including biotech or pharma. Strong ...

20BLOC

Process Scientist/Engineer

Thousand Oaks, CA · On-site

$90K/yr

We are looking for a motivated, hands-on Process Scientist/Engineer to join our team. This person ... Minimum 4 years' experience in bioprocessing environments including biotech or pharma. Strong ...

next page

Showing results 1-20

All JobsBiotech Process Engineer JobsBiotech Process Engineer Jobs in Los Angeles, CA

Biotech Process Engineer information

See Los Angeles, CA salary details

$53.3K

$99.2K

$153.5K

How much do biotech process engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for biotech process engineer in Los Angeles, CA is $99,150.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,300.00 and $111,000.00 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 are popular job titles related to Biotech Process Engineer jobs in Los Angeles, CA?

For Biotech Process Engineer jobs in Los Angeles, CA, the most frequently searched job titles are:

What job categories do people searching Biotech Process Engineer jobs in Los Angeles, CA look for?

The top searched job categories for Biotech Process Engineer jobs in Los Angeles, CA are:

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

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

Biotech Process Engineer jobs near you
Infographic showing various Biotech Process Engineer job openings in Los Angeles, CA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $99,150 per year, or $47.7 per hour.

Engineer, Biotech Process Engineering

3 Key Consulting

Newbury Park, CA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Engineer, Biotech Process Engineering

3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.

Job Summary:

Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our Thousand Oaks facility. Providing process engineering support for human therapeutic products in clinical development through commercial production, our mission is to translate developmental processes to commercial reality for patients through scientific expertise and engineering innovation. The Engineer will apply purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology. Will partner with manufacturing, quality, analytical, and bench scientists to support a highly dynamic manufacturing facility.

Job Responsibilities:

  • Transfer purification drug substance processes and performs process improvements from the laboratory into the manufacturing facility
  • Provide technical support for successful scale-up, transfer of process technology, and for clinical and/or commercial manufacturing operation.
  • Offer process validation support for late-stage commercial processes.
  • Provide routine process monitoring and troubleshooting.
  • Execute data trending and statistical process analysis.
  • Support technical direction for process related deviations, CAPAs and change controls.
  • Identify and support process related operational excellence opportunities.
  • Represent process development and collaborates with other functions such as Manufacturing, Quality, and Regulatory

Basic Qualifications:

  • Master's degree OR
  • Bachelor's degree OR
  • Associate's degree and 7 years of Engineering or Operations experience OR
  • High school diploma / GED and 8 years of Engineering or Operations experience

Preferred Qualifications:

  • Master's Degree in Chemical or Biochemical Engineering
  • 1+ years of Process Engineering experience preferably related to scale-up principles and commercial cGMP manufacturing facilities
  • Background in biologics tech transfer into commercial facilities
  • Purification process knowledge:
    • Knowledge of purification processes/ equipment; scale up factors from, chromatography, UF/DF, process deviations, raw materials to growth and quality attributes
    • Strong capability of analysis, troubleshooting and problem solving
    • Ability to develop and follow detailed protocols
    • Independently motivated with ability to multi-task and work in teams
    • Excellent written and verbal communication skills with technical writing and presentation experience

Top Must Have Skill Sets:

  • Must have biotech background/experience, plus must have purification experience.
  • Strong understanding of data analysis tools.
  • Knowledge of biologics purification processes/ equipment; scale up factors from, chromatography.
  • 1+ years of Process Engineering experience preferably related to scale-up principles and commercial cGMP manufacturing facilities.
  • Manufacturing experience must be biotech experience.

Day-To-Day Responsibilities:

Staff will perform tech transfer of early clinical candidate molecules. In addition, staff will support all processes (clinical and commercial) executed in the facility, performing process monitoring and responding to issues as appropriate.

Red Flags:

  • Multiple short duration jobs on resume
  • No purification experience - critical experience (Chromatography, purification, USTF)
  • Manufacturing experience - must be biotech experience

Interview Process:

Phone screen followed by Webex interview

We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you're not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.

Apply