3key Consulting, Inc.
Engineer, Drug Product Development, Process Design & Experimentation - Hybrid (
3key Consulting, Inc., Thousand Oaks, California, United States, 91362
Job Title:
Engineer, Drug Product Development, Process Design & Experimentation - Hybrid (JP14756)
Location:
Thousand Oaks, CA. 91320
Employment Type:
Contract
Business Unit:
Commercial Drug Product
Duration:
1+ year(s) (with likely extensions and/or conversion to permanent)
Posting Date:
11/18/25
Pay Rate:
$36 - $41/hour W2
Notes:
Only qualified candidates need apply. Hybrid - 2-3 days onsite per week. Flexibility for more onsite requirements may be necessary.
Job Description: This is a hybrid position. 2-3 days onsite per week. Must have flexibility for more onsite work if necessary.
Our ideal candidate will have a B.S. and 2YOE in Pharma with drug product experience.
As a member of the process development team, this role will be focused on identifying and developing aspects of drug product to advance process design for parenteral drug products. The candidate will perform experiments, organize data and analyze results with minimal supervision. The candidate will establish the experimental design, develop and implement protocols, obtain reproducible and reliable results, analyze data and communicate results to cross functional groups.
Why is the Position Open? Supplement additional workload on team.
Top Must Have Skills:
Good documentation practices (GDP)
Experience with visual inspection
Technical writing skills
Day to Day Responsibilities:
Supports the establishment of robust tactical and strategic objectives related to visual inspection
Supports ongoing development in the area of visual inspection (i.e. development and maintenance of defect panels, establishment of GMP procedures related to operations)
Implements and documents off-line and on-site drug product characterization studies
Author and/or own high-quality process technology transfer and other technical documents
Participate in cross-functional teams working effectively in a highly matrixed team environment to drive change, efficiency, and strong relationships
Provide ongoing support to clinical and commercial fill/finish manufacturing operations through troubleshooting, root cause analysis, and product impact assessments for non-conformance investigations and process changes/improvements
Design, execute and document primary data packages related to drug product design and process development, and communicate key findings in presentations
Support one or more clinical and commercial process introductions or process transfers into client manufacturing network
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:
2+ years of experience within the pharmaceutical/biotechnology industry
Experience in development/characterization of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters
Organizational, technical problem solving, communication (written and verbal) skills, and regular interactions
Ability to learn and act on dynamic information at a rapid pace
Familiar or ability to learn to use electronic record keeping, GMP, laboratory notebooks, statistical analysis and software.
Strong knowledge of quality systems and drug product manufacturing
Experience in a matrix team environment and interacting with Analytical Sciences, Process Development, Project Management, Manufacturing, Regulatory, Compliance, and/or Quality
Capable of organizing and communicating complex technical concepts to enable business decisions
Red Flags: No prior Pharma or Biotech experience.
Interview Process:
2 interviews (manager and team)
Video via Microsoft Teams
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
#J-18808-Ljbffr
Engineer, Drug Product Development, Process Design & Experimentation - Hybrid (JP14756)
Location:
Thousand Oaks, CA. 91320
Employment Type:
Contract
Business Unit:
Commercial Drug Product
Duration:
1+ year(s) (with likely extensions and/or conversion to permanent)
Posting Date:
11/18/25
Pay Rate:
$36 - $41/hour W2
Notes:
Only qualified candidates need apply. Hybrid - 2-3 days onsite per week. Flexibility for more onsite requirements may be necessary.
Job Description: This is a hybrid position. 2-3 days onsite per week. Must have flexibility for more onsite work if necessary.
Our ideal candidate will have a B.S. and 2YOE in Pharma with drug product experience.
As a member of the process development team, this role will be focused on identifying and developing aspects of drug product to advance process design for parenteral drug products. The candidate will perform experiments, organize data and analyze results with minimal supervision. The candidate will establish the experimental design, develop and implement protocols, obtain reproducible and reliable results, analyze data and communicate results to cross functional groups.
Why is the Position Open? Supplement additional workload on team.
Top Must Have Skills:
Good documentation practices (GDP)
Experience with visual inspection
Technical writing skills
Day to Day Responsibilities:
Supports the establishment of robust tactical and strategic objectives related to visual inspection
Supports ongoing development in the area of visual inspection (i.e. development and maintenance of defect panels, establishment of GMP procedures related to operations)
Implements and documents off-line and on-site drug product characterization studies
Author and/or own high-quality process technology transfer and other technical documents
Participate in cross-functional teams working effectively in a highly matrixed team environment to drive change, efficiency, and strong relationships
Provide ongoing support to clinical and commercial fill/finish manufacturing operations through troubleshooting, root cause analysis, and product impact assessments for non-conformance investigations and process changes/improvements
Design, execute and document primary data packages related to drug product design and process development, and communicate key findings in presentations
Support one or more clinical and commercial process introductions or process transfers into client manufacturing network
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:
2+ years of experience within the pharmaceutical/biotechnology industry
Experience in development/characterization of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters
Organizational, technical problem solving, communication (written and verbal) skills, and regular interactions
Ability to learn and act on dynamic information at a rapid pace
Familiar or ability to learn to use electronic record keeping, GMP, laboratory notebooks, statistical analysis and software.
Strong knowledge of quality systems and drug product manufacturing
Experience in a matrix team environment and interacting with Analytical Sciences, Process Development, Project Management, Manufacturing, Regulatory, Compliance, and/or Quality
Capable of organizing and communicating complex technical concepts to enable business decisions
Red Flags: No prior Pharma or Biotech experience.
Interview Process:
2 interviews (manager and team)
Video via Microsoft Teams
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
#J-18808-Ljbffr