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Abcellera Biologics Process Development Engineer Jobs

Huntsman

Process Development Engineer

Mcintosh, AL

: Process Development Engineer Huntsman is seeking a Process Development Engineer supporting the ADMAT Division located at the McIntosh Site . This position will report to the Site PD Manager . Job ...

SpaceX

Process Development Engineer

Hawthorne, CA · On-site

$110K - $135K/yr

PROCESS DEVELOPMENT ENGINEER - BUILD RELIABILITY The Process Development Engineer is responsible for developing and improving business processes and systems that enable SpaceX to design, build ...

SpaceX

Process Development Engineer

Hawthorne, CA · On-site

$110K - $135K/yr

PROCESS DEVELOPMENT ENGINEER - BUILD RELIABILITY The Process Development Engineer is responsible for developing and improving business processes and systems that enable SpaceX to design, build ...

SpaceX

Process Development Engineer

Hawthorne, CA

$110K - $135K/yr

PROCESS DEVELOPMENT ENGINEER - BUILD RELIABILITY The Process Development Engineer is responsible for developing and improving business processes and systems that enable SpaceX to design, build ...

Solidigm

Process Development Engineer

Rancho Cordova, CA · On-site

$139K - $223K/yr

As a Process Development Engineer at Solidigm you will be responsible for delivering module capability for the next node on the 3D NAND technology roadmap, partnering with the module process ...

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All JobsAbcellera Biologics Process Development Engineer Jobs

Abcellera Biologics Process Development Engineer information

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$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.

Sr Engineer, PD Process Validation & Business - Holly Springs, NC

National Guard Employment Network

Holly Springs, NC • On-site

$75K - $100K/yr

Full-time

Posted 13 days ago

Job description

Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
What you will do
Let's do this. Let's change the world. In this vital role you will be a part of the Process Development Drug Substance Technology group (PD DST) at Amgen's FleX Batch Biologics Manufacturing Facility. This position is part of the Process Validation & Business Strategy (PBS) team within PD DST. This role will be immersed in all aspects of operations in a commercial bulk drug substance facility, which includes development, support, and execution of process validation. The role will be responsible for ensuring process validation activities are performed in a consistent and controlled manner to support manufacture of drug substances. In addition, the role will be responsible for driving PD business strategy activities and providing cross-functional tech transfer support.
Lead the development of Process Validation/Process Performance Qualification strategy for New Products, ensuring alignment with regulatory guidelines and industry standards.
Apply a fundamental understanding of Upstream (Cell Culture) and Downstream (Purification) bioprocessing to support process validation, technology transfer support, and plant start-up
Lead the execution of validation projects and/or protocols and the collection of data to ensure completion of process validation activities.
Provide cross-functional process monitoring support as needed
Provide guidance for the generation, resolution and closure of deviations.
Lead ANC PD business strategy activities to improve network practice, develop digital tools, and optimize the ANC PD business operations
Ensure safety and compliance of process development activities
Provide process validation floor process support as required
Lead process validation support for regulatory filing, inspection, and other CMC activities
Additional Qualifications/Responsibilities
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The experienced scientific professional we seek is a leader with these qualifications.
Basic Qualifications:
  • High school diploma / GED and 10 years of biologics process development, process engineering, or process validation experience OR
  • Associate's degree and 8 years of biologics process development, process engineering, or process validation experience OR
  • Bachelor's degree and 4 years of biologics process development, process engineering, or process validation experience OR
  • Master's degree and 2 years of biologics process development, process engineering, or process validation experience OR
  • Doctorate degree

Preferred Qualifications:
  • 5+ years of experience in a process validation or downstream (purification) role supporting biopharmaceutical manufacturing processes within regulated environments (i.e., cGMP)
  • Strong and in-depth expertise of the operation of upstream and downstream manufacturing processes
  • Validation experience with biopharmaceutical processes including PPQ, master plans, protocols, and reports
  • Independently motivated with successful ability to multi-task and work in teams
  • Demonstrated leadership skills and decision-making experience
  • Experience in process scale-up, technology transfers, EBRs, deviation, CAPA, and change control processes.
  • Excellent oral and verbal communication skills, interact effectively with diverse internal and external stakeholders

Salary Range
115,494.60USD -156,257.40 USD

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