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Added 1 day ago
Sr. Robotics Engineer, kuka, ABB, and Fanuc, Biopharma (JP16096)
3 Key Consulting
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Top Must Have Skills:
Added 1 day ago
3K
Human Factors Engineer (Remote) – Combination Product Drug Delivery Devices & Usability Validation - (JP16090)
3 Key Consulting
Remote, United States
- $76 to $84 USD / hour
Top Must Have Skills:
Added 5 days ago
Engineer – Biotech Process Equipment Digital Automation, APIs/PLC/Python - (JP16092))
3 Key Consulting
New Albany, OH
Top Must Have Skills:
Added 5 days ago
3K
Engineer – GMP Drug Product Manufacturing Equipment & Reliability - (JP16085)
3 Key Consulting
Thousand Oaks, CA
- $41 to $46 USD / hour
Top Must Have Skills:
Added 5 days ago
3K
Engineer – GMP Drug Product Manufacturing Equipment & Reliability (JP16083)
3 Key Consulting
Thousand Oaks, CA
- $41 to $46 USD / hour
Top Must Have Skills:
Added 6 days ago
3K
Engineer, Primary Container Testing, Characterization & Qualification - Biopharma/Medical Device - (JP16093)
3 Key Consulting
Thousand Oaks, CA
- $40 to $46 USD / hour
Top Must Have Skills:
Added 7 days ago
3K
Associate Engineer – Primary Container Testing, Characterization & Qualification (Biopharmaceuticals) - JP16067
3 Key Consulting
Thousand Oaks, CA
- $30 to $33 USD / hour
Thousand Oaks, CA 91320 (hybrid; onsite 3 days per week) · Must be able to work onsite in Thousand Oaks, CA three days per week
Added 8 days ago
3K
Associate Engineer – Primary Container Testing, Characterization & Qualification (Biopharmaceuticals) - (JP16064)
3 Key Consulting
Thousand Oaks, CA
- $30 to $33 USD / hour
Top Must Have Skills:
Added 12 days ago
Engineer – GMP Physical Test Method Development & Validation (Combination Products) - (JP16052)
3 Key Consulting
Thousand Oaks, CA
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Added 18 days ago
Engineer – Physical Test Method Development & Validation (Medical Devices / Combination Products) - JP16020
3 Key Consulting
Ca, MA
Top Must Have Skills:
Added 21 days ago
3K
Senior Bioprocess Equipment Engineer – AI-Enabled Troubleshooting/Solutions - (JP16015)
3 Key Consulting
Thousand Oaks, CA
- $43 to $48 USD / hour
Top Must Have Skills:
Added 26 days ago
Quality Assurance Associate, Biopharma Medical Device (JP9524)
3 Key Consulting
Thousand Oaks, CA
Must have experience with GMP processes and documentation
Added 26 days ago
3K
Associate, Biopharma Lab-based (JP9644)
3 Key Consulting
Thousand Oaks, CA
- $20 to $22 USD / hour
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Added 26 days ago
Engineer - Packaging - (JP9673)
3 Key Consulting
Thousand Oaks, CA
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Added 26 days ago
3K
Sourcing Associate - ESS (JP9649)
3 Key Consulting
Tampa, FL
- $20 to $22 USD / hour
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Added 26 days ago
Senior Associate, Scientific Lab HPLC - (JP9677)
3 Key Consulting
Thousand Oaks, CA
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Added 26 days ago
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3 Key Consulting
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Added 26 days ago
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Senior Associate Quality Control - (JP9706)
3 Key Consulting
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3 Key Consulting
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- $30 to $33 USD / hour
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Added 26 days ago
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3 Key Consulting
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Added 26 days ago
Associate Quality Control – (JP9950)
3 Key Consulting
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Added 26 days ago
Metrology Engineer - (JP9956)
3 Key Consulting
Thousand Oaks, CA
Candidate must possess the ability to perform calibration and measurement systems with minimal supervision
Added 26 days ago
IS Analyst Senior Associate - Digital Workplace (JP9973)
3 Key Consulting
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Note: Onsite 3 days per week Thousand Oaks · Top Must have Skill Sets:
Added 26 days ago
MCS Manufacturing Associate, Biopharma (JP9784)
3 Key Consulting
Thousand Oaks, CA
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3 Key Consulting

Engineer, Drug Product Development, Process Design & Experimentation - Hybrid (JP14756)

Thousand Oaks, CA, United States

Hybrid

$36 to $41 USD / hour · Contract

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Job details

Pay: $36 to $41 USD / hour
Job type: Contract
Workplace: Hybrid
Experience: 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
Posting language: English
Posted: Nov 18, 2025

Original job description

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:

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.

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More about this job

Skills

Design process
Documentation
Inspection
Technical writing
Good manufacturing practices
Troubleshooting
Root cause analysis
Presentation skills
Biotechnology
Problem solving
Communication skills
Record keeping
Statistics
Quality control systems
Project management
Regulatory compliance
Microsoft Teams

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