About this opportunity
3 Key Consulting, Inc. lists this Process Development Engineer – Aseptic Fill-Finish, Tech Transfer & Validation (JP15893) opportunity in thousand oaks, California. Review the employer’s description below for duties, qualifications and application requirements.
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
Red Flags
No experience in biotech
Fresh out of college. Looking for someone with college and a few YOE
25 min (1:1) Hiring Manager
25 min (1:1) Technical and Team Collaboration Interview: L5 Senior Engineer (TBD)
25 min (1:1) Process Development Leadership Interview
#J-18808-Ljbffr
Worksite address
thousand oaks, CA, 91362, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.