Title: Valdiation Engineer (Medical Device) Location: Rochester NY Duration: 12 Months Overview: This role supports validation activities for new products within a medical device manufacturing ...
Title: Valdiation Engineer (Medical Device) Location: Rochester NY Duration: 12 Months Overview: This role supports validation activities for new products within a medical device manufacturing ...
Demonstrated experience in applying statistical techniques to real-world problems, particularly in the medical device industry. * Demonstrated experience in systems engineering tools and ...
Demonstrated experience in applying statistical techniques to real-world problems, particularly in the medical device industry. * Demonstrated experience in systems engineering tools and ...
Demonstrated experience in applying statistical techniques to real-world problems, particularly in the medical device industry. * Demonstrated experience in systems engineering tools and ...
Demonstrated experience in applying statistical techniques to real-world problems, particularly in the medical device industry. * Demonstrated experience in systems engineering tools and ...
Demonstrated experience in applying statistical techniques to real-world problems, particularly in the medical device industry. * Demonstrated experience in systems engineering tools and ...
Demonstrated experience in applying statistical techniques to real-world problems, particularly in the medical device industry. * Demonstrated experience in systems engineering tools and ...
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... Engineering, or Physical Science is preferred. * Must have at least 5 years of related experience in Medical Device quality system management, including experience in working under Design Control.
... Engineering, or Physical Science is preferred. * Must have at least 5 years of related experience in Medical Device quality system management, including experience in working under Design Control.
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Internship R D Engineer Medical Device information
See Rochester, NY salary details
$10.91 - $12.57
2% of jobs
$12.57 - $14.23
4% of jobs
$15.89 is the 25th percentile. Wages below this are outliers.
$14.23 - $15.89
19% of jobs
$15.89 - $17.55
24% of jobs
The median wage is $17.66 / hr.
$17.55 - $19.21
17% of jobs
$20.21 is the 75th percentile. Wages above this are outliers.
$19.21 - $20.87
16% of jobs
$20.87 - $22.53
6% of jobs
$22.53 - $24.19
5% of jobs
$24.19 - $25.85
3% of jobs
$25.85 - $27.51
3% of jobs
$27.51 - $29.17
1% of jobs
$10
$19
$29
How much do internship r&d engineer medical device jobs pay per hour?
What does an Internship R&D Engineer in Medical Device do?
What are the key skills and qualifications needed to thrive as an Internship R&D Engineer in Medical Devices, and why are they important?
What is the difference between Internship R&D Engineer Medical Device vs R&D Engineer Medical Device?
| Aspect | Internship R&D Engineer Medical Device | R&D Engineer Medical Device |
|---|---|---|
| Qualifications | Enrolled in or recent graduate of engineering/biomedical programs | Bachelor's or Master's in engineering/biomedical fields |
| Work Environment | Internship programs, entry-level projects, supervised tasks | Full-time, independent project work, team collaboration |
| Responsibilities | Assisting in research, testing, and documentation | Design, develop, and improve medical device products |
| Industry Usage | Commonly used for training and entry-level experience | Core role in product development and innovation |
In summary, the Internship R&D Engineer Medical Device is an entry-level position designed for students or recent graduates gaining initial industry experience. The R&D Engineer Medical Device is a full-time professional role with greater responsibilities in product development and innovation within the medical device industry.
What types of projects or tasks can an Internship R&D Engineer expect to work on in the medical device industry?

Job description
Title: Valdiation Engineer (Medical Device)
Location: Rochester NY
Duration: 12 Months
Overview:
This role supports validation activities for new products within a medical device manufacturing facility and requires the ability to work both independently and as part of a cross-functional team.
Key Responsibilities
Support validation work for new products, including laboratory testing utilizing VITROS analyzers.
Prepare and handle clinical test specimens according to approved procedures, best practices, and safety requirements, including appropriate PPE.
Perform pilot-scale formulations with biological materials, as needed.
Operate and maintain laboratory equipment; complete all required documentation in real time (QC records, instrument logs, test records).
Independently execute laboratory experiments and assist with troubleshooting instrument and test failures, as needed.
Review and analyze data; document conclusions and test summaries in appropriate quality records within QuidelOrtho's quality system.
Ensure organization, documentation, and tracking of long-term studies with multiple factors, products, and conditions.
Maintain a working knowledge of cGMP requirements and adhere to all quality, regulatory, and safety guidelines.
This role involves both laboratory and computer-based work.
Skills Required:
Bachelor's degree in a scientific field (e.g., Chemistry, Biology, or equivalent) required.
Experience in an FDA-regulated industry and in validation for medical devices preferred.
Familiarity with VITROS products and VITROS analyzers highly desired.
Familiarity with biological formulations and processing techniques highly desired.
Strong written and verbal communication skills with excellent attention to detail required.
Strong organizational skills and ability to manage complex, long-term studies required.
Proficiency in Excel required, with additional statistical analysis skills preferred.
About Caresoft
Sourced by ZipRecruiter
Industry
It services
Company size
51 - 200 Employees
Headquarters location
Somerset, NJ, US
Year founded
1994