Process Development Engineer – Aseptic Fill-Finish, Tech Transfer & Validation (JP15893)

3 Key Consulting, Inc.

Thousand Oaks (CA)

On-site

USD 56,000 - 63,000

Full time

6 days ago

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Job summary

3 Key Consulting, Inc. is seeking a Process Development Engineer for aseptic fill-finish, tech transfer, and validation in Thousand Oaks, CA on a contract basis. The role emphasizes PD and PM with potential extensions.

Bachelor or Master degrees and experience in drug manufacturing environments are valued. The candidate will support characterization, validation, and technology transfer activities across multiple lines, coordinating with cross-functional teams to generate robust data packages and

Qualifications

Bachelor's or Master’s degree in science or engineering with applicable experience.
Experience with software tools beyond Microsoft Office, such as SAP or Smartsheet.
Drug product knowledge not required but helpful; strong documentation skills.

Responsibilities

Apply engineering and scientific principles to resolve process issues and evaluate improvements.
Design and execute experiments to characterize capabilities and enable process changes.
Support technology transfer leads during drug product transfers to clinical and commercial sites.
Develop and maintain technology transfer tools and data analytics solutions.
Communicate results and document protocols, assessments, and reports.

Skills

Cross-functional communication

Critical thinking

Accountability

Drug manufacturing experience

Education

Master's degree

Bachelor's degree + 2 years

Associate degree + 6 years

High school diploma / GED + 8 years

Tools

SAP

Smartsheet

Minitab

JMP

Job description

Job Title: Process Development Engineer - Aseptic Fill-Finish, Tech Transfer & Validation (JP15893)

Location: Thousand Oaks, CA. 91320

Employment Type: Contract

Business Unit: Commercial Drug Product

Duration: 1+ year (with likely extensions and/or conversion to permanent)

Posting Date: 09/23/26

Pay Rate: $41 - $46/hour W2

Notes: Only qualified candidates need apply.

Job Description

The ideal candidate for this role should have a bachelor's degree in a scientific or engineering discipline. Candidates with a recent master's degree may also be suitable if they demonstrate strong interpersonal and communication skills. The candidate should have experience with software tools beyond Microsoft Office, such as SAP or Smartsheet, although these tools can be learned on the job. Prior drug product knowledge is not required; however, the candidate should excel in group coordination, meeting deadlines, and maintaining meticulous documentation.

This position emphasizes process development (PD) and project management (PM) skills, with technical expertise expected to develop over time.

As a member of the Process Development team, the candidate will support senior staff in developing and characterizing drug product technologies and manufacturing capabilities. The candidate will also assist with process validation and technology transfer activities for multiple products across various production lines at our client's aseptic fill-finish manufacturing facilities in Thousand Oaks, CA.

The candidate will support senior staff in planning, executing, and documenting characterization, process validation, and technology transfer projects. The candidate will be primarily responsible for executing characterization studies and other experiments at laboratory and production scales to generate technical data packages using complex technologies, while organizing data and analyzing results under the supervision of senior staff.

The candidate will interface with various drug product teams to support the successful technology transfer of products and the associated documentation. The candidate will assist in establishing experimental designs, developing and executing protocols, obtaining reproducible and reliable results, analyzing and documenting experimental results, and communicating findings to cross-functional groups

Why is the Position Open?

Supplement additional workload on team

Top Must Have Skills

Cross-functional communication and collaboration
Critical thinking, scientific and technical execution
Accountability and time management
Experience with drug manufacturing processes or drug substances are preferred but not required

Day to Day Responsibilities

Apply fundamental engineering and scientific principles to resolve issues and evaluate the effects of process improvements, equipment, scale, and raw materials.
Assist in the design and execution of experiments to characterize and enable the implementation of new capabilities and process changes, such as filling, lyophilization, and analytical technologies.
Support technology transfer leads during the transfer of drug products to clinical and commercial manufacturing sites, including make-a-batch exercises, process parameter risk assessments, process transfer documents, and change control assessments.
Support the development and maintenance of clinical and commercial technology transfer tools.
Effectively communicate the results of characterization studies, experimental execution, and technology transfer initiatives.
Author, review, and data-verify technical documents, such as technical protocols, technical assessments, technical reports, draft standard operating procedures, and guidance documents.
Analyze generated data, including performing statistical analyses using Minitab, JMP, or similar software.
Develop digital tools and models by leveraging data analytics and programming skills.
Support at-scale characterization and/or process validation runs as a person in plant.
Support the planning, execution, and documentation of process development, characterization, process validation, and technology transfer activities.
Execute laboratory- and production-scale experiments, including protocol preparation, experimental setup, and data collection.
Organize, analyze, and interpret technical data using tools such as Minitab, JMP, SAP, and Smartsheet.
Track project activities, deliverables, and timelines while proactively communicating risks or delays.
Collaborate with cross-functional teams and manufacturing sites to support drug product technology transfers.
Assist with process risk assessments, change control evaluations, make-a-batch exercises, and transfer documentation.
Communicate study results, technical findings, and project updates to senior staff and cross-functional stakeholders.
Support characterization and process validation runs at manufacturing scale as a person in plant.
Develop and maintain technology transfer tools, data analytics solutions, and process models.

Basic Qualifications

Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience

Preferred Qualifications

B.S. in a scientific or engineering discipline with 1-3 years of experience, or M.S. in a scientific or engineering discipline with 0-2 years of experience.
Familiarity with cGMP and experience in drug product or drug substance manufacturing or process development.
Knowledge of and hands‑on experience with various drug product technologies.
Demonstrated critical thinking, problem-solving, and independent research skills.
Ability to learn new techniques, perform multiple tasks, maintain accurate records, follow instructions, and comply with company policies.
Excellent project management skills and the ability to elevate relevant issues to the project lead and line management.
Strong cross-functional teamwork and effective oral and written communication skills.
Ability to work independently and collaboratively with internal and external partners.
Strong computer and organizational skills, with close attention to detail.
Self‑motivated with a positive attitude.

Employee Value Proposition

Supplement additional workload on team

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