ZipRecruiter

Log In

1

Abcellera Biologics Process Development Engineer Jobs

Inteva Products

Process Development Engineer

Troy, MI · On-site

Description The Process Development Engineer will lead advanced development initiatives focused on new and emerging manufacturing processes, from concept through production implementation. This is a ...

FITS LLC

Process Development Engineer

Dorado, PR · On-site

For Process Development services in the Process Engineering area. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor Degree in Engineering ( Mechanical or Electrical ) and at least five (5) years ...

Teleflex

Process Development Engineer

Trenton, GA

... process development and design to meet customer product requirements. Provide engineering support of products as they advance into production. Lead major projects involving capital improvement ...

Nokia

Process Development Engineer

Allentown, PA

The person should have hands-on experience with process development and be well versed in mechanical engineering or materials science as well as with automated equipment in a high-volume ...

Nokia

Process Development Engineer

Allentown, PA · On-site

The person should have hands-on experience with process development and be well versed in mechanical engineering or materials science as well as with automated equipment in a high-volume ...

Periodic Labs

Process Development Engineer

Menlo Park, CA · On-site

$175K - $275K/yr

About the Role As a Process Development Engineer, you will play a crucial role in designing and optimizing the workflows and tools that enable high-efficiency process technologies, primarily for the ...

Teledyne

Process Development Engineer

Goleta, CA · On-site

$90K - $121K/yr

As part of the uncooled detector (focal plane array) research and development team, the successful candidate will have responsibility for engineering wafer fab processes including DUV lithography ...

next page

Showing results 1-20

All JobsAbcellera Biologics Process Development Engineer Jobs

Abcellera Biologics Process Development Engineer information

See salary details

$49.5K

$92K

$142.5K

How much do abcellera biologics process development engineer jobs pay per year?

As of Jun 9, 2026, the average yearly pay for abcellera biologics process development engineer in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What jobs make $3,000 a month without a degree?

Jobs such as process development technicians or manufacturing operators in biotech companies like Abcellera Biologics can earn around $3,000 monthly without a degree, especially with relevant technical skills and experience. These roles often require on-the-job training, familiarity with laboratory or production environments, and sometimes certifications, but typically do not mandate a college degree.
What cities are hiring for Abcellera Biologics Process Development Engineer jobs? Cities with the most Abcellera Biologics Process Development Engineer job openings:
Infographic showing various Abcellera Biologics Process Development Engineer job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 84% Full Time, and 15% Part Time. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

Process Development Engineer

Mirus Consulting Group

Dorado, PR

Other

Posted 24 days ago

Job description

mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved.
Role Summary
The Process Development Engineer supports the development, validation, and implementation of new manufacturing processes. The role involves equipment and process validation, documentation generation, process optimization, and cross-functional technical collaboration.
Key Responsibilities

  • Support IQ/OQ/PQ and process performance qualification activities; develop validation protocols, reports, and master validation plans.
  • Design and develop inprocess and receiving inspection systems for new components and processes.
  • Generate equipment documentation (evaluations, PM/calibration procedures) and manufacturing instructions.
  • Manage process development projects from concept through implementation; collaborating with cross-functional teams.
  • Apply DOE, PFMEA, and risk analysis to characterize, optimize, and improve manufacturing processes.
  • Work with technologies such as laser welding, heat bonding, injection molding, vision systems, and automation (PLC/servo/pneumatics/sensors).
Process Characterization & Reporting Activities
  • Evaluate current manufacturing process flows and identify gaps and improvement opportunities.
  • Analyze product requirements to ensure alignment with manufacturing capabilities.
  • Assess manufacturability and scalability of processes.
  • Review historical process data, including yield trends, scrap rates, and process capability.
  • Perform time studies and cycle time analysis to optimize efficiency.
  • Execute Design of Experiments (DOE) studies for process characterization and optimization.
  • Develop and maintain PFMEA documentation.
  • Conduct engineering assessments to support decision-making and technical justification.
  • Create and maintain process flow diagrams.
  • Develop automation concepts to improve process capability and efficiency.
  • Perform feasibility studies for new processes, technologies, or equipment.
  • Conduct risk assessments to identify and mitigate process risks.
  • Define validation strategies, including preliminary validation approaches for new and existing processes.
Experience Requirements
  • 5-7+ years in manufacturing engineering or quality engineering within an FDAregulated environment (medical devices, pharma, diagnostics, biotech).
  • Strong working knowledge of 21 CFR Part 820, GMP, and ISO 13485.
  • Electrical and mechanical engineering background applied to automated manufacturing systems.
  • Experience with automation/controls, tooling, fixtures, test method development, and equipment qualification.
  • Proficiency in DOE, FMEA, CAPA, and rootcause investigation.
  • Experience supporting new product introductions and process scaleup.

This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.

Apply