Engineer Senior
Apply NowCompany: Crystal Equation
Location: Thousand Oaks, CA 91360
Description:
Job Description
Engineer Senior
Hybrid
Top 3 Must Have Skill Sets:
Red Flags:
The Device Engineer will participate in the medical device/combination product design, development, and commercialization activities for drug delivery devices, focusing on prefilled syringes.
Responsibilities:
Preferred Qualifications:
Pay range is $38/hr - $43/hr 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.
Meet Your Recruiter
Krista McIlwaine
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Engineer Senior
Hybrid
Top 3 Must Have Skill Sets:
- Pharma background.
- Physical testing experience
- Design controls experience
Red Flags:
- Poor communication skills
- Lack of hands on testing experience
The Device Engineer will participate in the medical device/combination product design, development, and commercialization activities for drug delivery devices, focusing on prefilled syringes.
Responsibilities:
- Leading test procedure development and functional test execution
- Leading material inventory management for prefilled syringe programs, including material forecasting and material custody across multiple sites and functional groups.
- Authoring technical plans and reports
- Performing advanced statistical data analysis
- Supporting Leading technical assessments and root cause investigations as well as planning and delegation of sub-tasks to other team members.
- Transfer of information to manufacturing sites, engagement with suppliers
- Maintenance of Design History File content consistent with Good Documentation Practices
- Training junior staff on physical test methods, sample preparation protocols and procedures, and effective report writing.
- Reviewing primary data collected from peers in support for various design controls activities, including characterization and design verification.
- Supporting design transfer activities by leading cross-functional coordination of sample procurement and testing.
- Supporting the setting of specification limits for platform devices through human factors studies benchtop testing.
- Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments.
- Plans and conducts work requiring judgment in the independent evaluation, selection, and adaptation and modification of standard techniques/procedures/criteria, and devises new approaches to encountered challenges.
- Generates and maintains design specifications, protocol and report writing, prototyping, design of experiments/statistical process control product optimization, design verification & validation, FMEA, etc.
- System level root cause investigation; CAD/SolidWorks proficiency; tolerance analysis; capability analysis.
- Coordinate and implement design improvements with development partners.
- Collaborate with scientists and engineers internally and externally to assess and develop appropriate design and manufacturing specifications.
- Accountability of maintaining technical records within product design history files.
- Individual contributor with leadership attributes to effectively represent device engineering within a large network/matrix organization.
- Working proficiency and familiarity with governing standards and regulations, including Quality System Regulation (21CFR820) and Risk Management (ISO 14971).
- Doctorate degree
- Master degree and 3 years of experience
- Bachelor degree and 5 years of experience
- Associate degree and 10 years of experience
- High school diploma / GED and 12 years of experience
Preferred Qualifications:
- Degree in the field of Mechanical or Biomedical Engineering, or related field
- Medical device industry and/or regulated work environment experience
- Excellent written and verbal communication skill
- Understanding and experience in:
- Development/commercialization of medical devices and knowledge of manufacturing processes
- Initiating and bringing complex projects to conclusion
- Ability to work independently and dynamic cross functional teams
- Design controls
- Failure investigation
- Applied statistics
Pay range is $38/hr - $43/hr 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.
Meet Your Recruiter
Krista McIlwaine
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