Crystal Equation
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Engineer
Top 3 Must Have Skill Sets:
Summary:
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.
Responsibilities:
Basic Qualifications:
OR
OR
OR
Preferred Qualifications:
Pay range is $31 - $36 per hour with full benefits available, including paid time off, medical/dental/vision/life insurance, 401K, parental leave, and more. Our compensation reflects the cost of labor across several US geographic markets. Pay is based on several factors including market location and may vary depending on job-related knowledge, skills, and experience.
THE PROMISES WE MAKE:
At Crystal Equation, we empower people and advance technology initiatives by building trust. Your recruiter will prep you for the interview, obtain feedback, guide you through any necessary paperwork and provide everything you need for a successful start. We will serve to empower you along the way and provide the path for your professional journey.
For more information regarding our Privacy Policy, please visit crystalequation.com/privacy.
Engineer
1 Amgen Center Dr. Thousand Oaks, CA 91320 US
Posted: 11/18/2025
2025-11-18
2026-01-05
Job Number: 41573
Job Description
Engineer
Top 3 Must Have Skill Sets:
- Good documentation practices (GDP)
- Experience with visual inspection
- Technical writing skills
- No prior Pharma or Biotech
Summary:
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.
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 our 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
Pay range is $31 - $36 per hour with full benefits available, including paid time off, medical/dental/vision/life insurance, 401K, parental leave, and more. Our compensation reflects the cost of labor across several US geographic markets. Pay is based on several factors including market location and may vary depending on job-related knowledge, skills, and experience.
THE PROMISES WE MAKE:
At Crystal Equation, we empower people and advance technology initiatives by building trust. Your recruiter will prep you for the interview, obtain feedback, guide you through any necessary paperwork and provide everything you need for a successful start. We will serve to empower you along the way and provide the path for your professional journey.
For more information regarding our Privacy Policy, please visit crystalequation.com/privacy.
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Ready to take your career to the next level in the vibrant city of Thousand Oaks, California? Nestled in the heart of Ventura County, this bustling city offers a perfect blend of suburban charm and urban amenities. With a strong job market, top-notch schools, and breathtaking views of the Santa Monica Mountains, Thousand Oaks is an ideal location for professionals seeking growth and fulfillment. Explore job opportunities near iconic sites like the Gardens of the World, catch a show at the Fred Kavli Theatre, or indulge in the local culinary scene featuring dishes from around the world. Join this dynamic community and unlock your potential in Thousand Oaks! Start your job search now to find your perfect fit in this captivating city.