Engineer, Drug Product Development, Process Design & Experimentation - Hybrid (JP14756)
3 Key Consulting · Thousand Oaks, CA ·
- Work mode
- Hybrid
- Employment
- Contract
- Category
- Design
- Experience
- 1+ years
- Salary
- USD 36 – 41 / hour
Designs and runs experiments to improve drug-product manufacturing processes, focusing on aseptic fill/finish and visual inspection, and documents results for cross-functional teams.
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.
3 Key Consulting is hiring an Engineer, Drug Product Development, Process Design & Experimentation - Hybrid for a consulting engagement with our direct client, a leading global biopharmaceutical company.
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:
Day to Day Responsibilities:
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:
Red Flags:
No prior Pharma or Biotech experience.
Interview process:
We invite qualified candidates to send your resume to [email protected]. 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.
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.
3 Key Consulting is hiring an Engineer, Drug Product Development, Process Design & Experimentation - Hybrid for a consulting engagement with our direct client, a leading global biopharmaceutical company.
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 [email protected]. 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.