Top 5 Cutera Jobs | SimplyHired

Staff Compliance Validation Engineer
CUTERA INC —Brisbane, CA
- $130,000 - $150,000 a year
- Full-time
- Engineering
- 8 years
- Analysis skills
Quick Apply
Manager, Clinical Research
CUTERA INC —Brisbane, CA
- $140,000 - $160,000 a year
- Full-time
- Microsoft Excel
- Management
- 5 years
Quick Apply
Principal Embedded Software Engineer
CUTERA INC —Brisbane, CA
- $175,000 - $200,000 a year
- Full-time
- Computer Science
- Software troubleshooting
- 11+ years
- Health insurance
Quick Apply
Clinical Applications Trainer (Northeast)
CUTERA INC —Brisbane, CA
- $90,000 - $110,000 a year
- Full-time
- RN License
- 5 years
- Travel
Quick Apply
Field Service Engineer (West)
CUTERA INC —Brisbane, CA
- $80,000 - $100,000 a year
- Full-time
- Military
- Bachelor of Science
- Mid-level
Quick Apply

More jobs to discover

Find similar jobs that you might be interested in.

Clinical Data Manager
MM Infotech —Remote
B.S. in life sciences or related field. 3+ years clinical data experience. Coordinate with clinical teams and statisticians.
Sr. Clinical Research Manager
Nutrafol —Remote
Bachelor's degree in related medical field. This role is hands-on and operationally embedded, with responsibility for claim substantiation support, study design…
$150,000 - $165,000 a year

I want to receive the latest job alert for cutera

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

cutera jobs near

Field Service Engineer jobs in Rhode Island

Oil Field jobs in Kentucky

Field Service Engineer jobs in Alabama

Field Service Engineer jobs in Hagerstown, MD

Packaging Engineer jobs in San Francisco Bay Area, CA

Answering Service jobs in Remote

Oil Field jobs in Norman, OK

Field Service Engineer jobs in Minneapolis, MN

Corporate Trainer jobs in St. Louis, MO

Map Trainer jobs in Massachusetts

College Athletic Trainer jobs in California

Athletic Trainer jobs in San Antonio, TX

Personal Trainer jobs in Miami, FL

Clinical Research Specialist jobs in Puyallup, WA

Clinical Research Specialist jobs in Wellington, FL

Clinical Research Specialist jobs in Toledo, OH

Clinical Research Specialist jobs in Remote

Clinical Research jobs in Minneapolis, MN

Entry Level Policy Research jobs in San Francisco, CA

Principal Software Engineer jobs in Germantown, MD

Staff Compliance Validation Engineer

CUTERA INC -
Brisbane, CA

Quick Apply

Job Details

Full-time
$130,000 - $150,000 a year

Qualifications

New product introduction
Engineering development testing
Embedded systems
ISO standards
Collaboration with product development teams
Production validation processes
Embedded software
Technology transfer (scale-up process)
Compliance documentation
Regulatory/legal compliance standards in production
Quality standards in production
Collaboration with manufacturing teams
Biomedical regulatory compliance
Test validation method
Production documentation
Cross-functional communication
FDA regulations

Full Job Description

Position Summary:

We are seeking an experienced Compliance and Validation Engineer to lead validation strategy and execution across products, embedded software, hardware, and manufacturing processes. This role is critical to ensure that our technologies meet global regulatory requirements while maintaining the high standards of performance, scalability, and reliability.

As a key partner to R&D and Manufacturing, you will drive a proactive, engineering-focused approach to validation supporting new product introductions (NPI), design transfers, and sustaining operations. This role focuses on executing effective validation activities and supporting the development of efficient, scalable, and audit-ready processes.

Duties & Responsibilities:

Lead the development and execution of validation strategies, protocols, and reports for equipment, systems, software, and manufacturing processes.
Own and drive qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), with a focus on production readiness.
Ensure compliance with applicable regulatory and quality standards (e.g., FDA, ISO 13485) through practical, engineering-driven validation approaches.
Partner cross-functionally with R&D and Manufacturing teams to support new product introduction (NPI), design verification/validation, and design transfer to production.
Support integration and validation of hardware/software systems, including test method development and execution.
Drive validation activities for manufacturing equipment, fixtures, and process development to ensure robust and repeatable production.
Author, review, and maintain validation documentation, ensuring accuracy, completeness, and audit readiness.
Support internal and external audits and regulatory inspections, serving as a subject matter expert for validation and compliance activities.
Develop and maintain SOPs and related documentation and deliver training to ensure consistent understanding and application of validation and compliance requirements.
Drive continuous improvement in validation and manufacturing processes, leveraging data-driven and engineering best practices.
Monitor evolving regulatory requirements and industry best practices, recommending and implementing improvements as needed.
Other duties as needed or required.

Minimum Requirements & Qualifications:

Bachelor’s degree in Engineering, Quality, or a related field; advanced degree preferred
8+ years of experience in validation engineering, quality, or compliance within a regulated industry (medical device, pharmaceutical, or biotechnology preferred).
Strong knowledge of validation principles, including IQ/OQ/PQ, with hands-on experience in software, hardware, and manufacturing environments.
Solid understanding of regulatory requirements and quality standards, including FDA regulations and ISO 13485.
Experience with embedded systems, hardware/software integration, and production test methodologies.
Familiarity with supporting NPI, design transfer, and manufacturing process validation.
Proficiency with quality management systems (QMS) and validation documentation practices.
Strong analytical, problem-solving, and organizational skills with high attention to detail.
Excellent communication and collaboration skills, with the ability to work effectively across engineering and manufacturing teams.

Preferred Qualifications:

Enterprise Architect
Markdown
Quarto
PowerShell, JavaScript, Typst (and other tools) for automating document generation.

Quick Apply

Refine Your Search

cutera jobs

Staff Compliance Validation Engineer

Manager, Clinical Research

Principal Embedded Software Engineer

Clinical Applications Trainer (Northeast)

Field Service Engineer (West)

More jobs to discover

I want to receive the latest job alert for cutera

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected