... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical
... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical
System Test and Validation Lead
Atlanta, GA · On-site +1
... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical
System Test and Validation Lead
Atlanta, GA · On-site +1
... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical
This role is focused on transforming validated needs into differentiated, testable, and scalable ... Bridge consumer design principles with medical device development rigor, ensuring solutions are ...
This role is focused on transforming validated needs into differentiated, testable, and scalable ... Bridge consumer design principles with medical device development rigor, ensuring solutions are ...
... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical
... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical
Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.
Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.
Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.
Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.
Software QA Engineer 1
Berkeley Lake, GA · On-site
... validation across: Cloud environments (AWS, Google Cloud Platform, Azure) Backend services and APIs ... medical device design controls is a plus)
Software QA Engineer 1
Berkeley Lake, GA · On-site
... validation across: Cloud environments (AWS, Google Cloud Platform, Azure) Backend services and APIs ... medical device design controls is a plus)
Embedded Firmware Engineer
Ball Ground, GA · On-site
$96K - $131K/yr
The Firmware Engineer will be responsible for providing cross-functional engineering project ... Familiarity with the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls ...
Embedded Firmware Engineer
Ball Ground, GA · On-site
$96K - $131K/yr
The Firmware Engineer will be responsible for providing cross-functional engineering project ... Familiarity with the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls ...
Embedded Firmware Engineer
Ball Ground, GA · On-site
$96K - $131K/yr
The Firmware Engineer will be responsible for providing cross-functional engineering project ... Familiarity with the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls ...
Quick apply
Embedded Firmware Engineer
Ball Ground, GA · On-site
$96K - $131K/yr
The Firmware Engineer will be responsible for providing cross-functional engineering project ... Familiarity with the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls ...
Embedded Firmware Engineer
$96K - $131K/yr
The Firmware Engineer will be responsible for providing cross-functional engineering project ... the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls or similar ...
Embedded Firmware Engineer
$96K - $131K/yr
The Firmware Engineer will be responsible for providing cross-functional engineering project ... the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls or similar ...
Medical Device, Medical Technology & Diagnostics; Generics; or, Animal Health; and, Consumer ... Key experience: (e.g., process engineering, process validation) and strong management consulting ...
Medical Device, Medical Technology & Diagnostics; Generics; or, Animal Health; and, Consumer ... Key experience: (e.g., process engineering, process validation) and strong management consulting ...
The successful candidate will bring expertise in medical device development, biomedical innovation, translational research, engineering, regulatory affairs, commercialization, or related fields and ...
The successful candidate will bring expertise in medical device development, biomedical innovation, translational research, engineering, regulatory affairs, commercialization, or related fields and ...
Serve as a subject matter expert on medical device lifecycle management, informing long-term ... Certified Clinical Engineer (CCE)Certified Healthcare Technology Manager (CHTM)Project Management ...
Serve as a subject matter expert on medical device lifecycle management, informing long-term ... Certified Clinical Engineer (CCE)Certified Healthcare Technology Manager (CHTM)Project Management ...
Serve as a subject matter expert on medical device lifecycle management, informing long-term ... Certified Clinical Engineer (CCE)Certified Healthcare Technology Manager (CHTM)Project Management ...
Serve as a subject matter expert on medical device lifecycle management, informing long-term ... Certified Clinical Engineer (CCE)Certified Healthcare Technology Manager (CHTM)Project Management ...
Company Description MiRus is a privately held medical device company focusing on the design and ... and validation plans and activities, test plan formation and execution to support regulatory ...
Quick apply
Company Description MiRus is a privately held medical device company focusing on the design and ... and validation plans and activities, test plan formation and execution to support regulatory ...
Serve as a subject matter expert on medical device lifecycle management, informing long-term ... Certified Clinical Engineer (CCE) Certified Healthcare Technology Manager (CHTM) Project Management ...
Serve as a subject matter expert on medical device lifecycle management, informing long-term ... Certified Clinical Engineer (CCE) Certified Healthcare Technology Manager (CHTM) Project Management ...
Serve as a subject matter expert on medical device lifecycle management, informing long-term ... Certified Clinical Engineer (CCE) Certified Healthcare Technology Manager (CHTM) Project Management ...
Serve as a subject matter expert on medical device lifecycle management, informing long-term ... Certified Clinical Engineer (CCE) Certified Healthcare Technology Manager (CHTM) Project Management ...
Sr Process Engineer (Mechanical Systems) - Radioisotope Manufact
Buford, GA · On-site
$67K - $88K/yr
... medical device, biotechnology, or radiopharmaceutical industries. * Knowledge of GMP manufacturing practices and validation requirements. * Experience supporting qualification and commissioning ...
Sr Process Engineer (Mechanical Systems) - Radioisotope Manufact
Buford, GA · On-site
$67K - $88K/yr
... medical device, biotechnology, or radiopharmaceutical industries. * Knowledge of GMP manufacturing practices and validation requirements. * Experience supporting qualification and commissioning ...
Sr Process Engineer (Mechanical Systems) - Radioisotope Manufact
Buford, GA · On-site
$67K - $88K/yr
... medical device, biotechnology, or radiopharmaceutical industries. * Knowledge of GMP manufacturing practices and validation requirements. * Experience supporting qualification and commissioning ...
Sr Process Engineer (Mechanical Systems) - Radioisotope Manufact
Buford, GA · On-site
$67K - $88K/yr
... medical device, biotechnology, or radiopharmaceutical industries. * Knowledge of GMP manufacturing practices and validation requirements. * Experience supporting qualification and commissioning ...
Sr Process Engineer (Mechanical Systems) - Radioisotope Manufact
Buford, GA · On-site
$67K - $88K/yr
... medical device, biotechnology, or radiopharmaceutical industries. * Knowledge of GMP manufacturing practices and validation requirements. * Experience supporting qualification and commissioning ...
Sr Process Engineer (Mechanical Systems) - Radioisotope Manufact
Buford, GA · On-site
$67K - $88K/yr
... medical device, biotechnology, or radiopharmaceutical industries. * Knowledge of GMP manufacturing practices and validation requirements. * Experience supporting qualification and commissioning ...
Medical Device Validation Engineer information
What does a medical device validation engineer do?
What are the key skills and qualifications needed to thrive as a medical device validation engineer?
What are some common challenges faced by medical device validation engineers during the validation process?
What is the difference between Medical Device Validation Engineer vs Quality Assurance Engineer?
| Aspect | Medical Device Validation Engineer | Quality Assurance Engineer |
|---|---|---|
| Credentials | Engineering degree, certifications like CQE or validation-specific training | Engineering or related degree, CQE or QA certifications |
| Work Environment | Design validation, process validation, testing labs | Audits, process improvements, compliance documentation |
| Industry Usage | Product development, validation phases in medical device manufacturing | Ensuring overall product quality, compliance, and process control |
The Medical Device Validation Engineer focuses on validating medical devices through testing and process validation, ensuring products meet regulatory standards. In contrast, the Quality Assurance Engineer oversees overall quality systems, audits, and compliance processes. Both roles require similar certifications and work within the medical device industry, but their core responsibilities differ in scope and focus.
What are popular job titles related to Medical Device Validation Engineer jobs in Georgia?
For Medical Device Validation Engineer jobs in Georgia, the most frequently searched job titles are:
What job categories do people searching Medical Device Validation Engineer jobs in Georgia look for?
The top searched job categories for Medical Device Validation Engineer jobs in Georgia are:
What cities in Georgia are hiring for Medical Device Validation Engineer jobs?
Cities in Georgia with the most Medical Device Validation Engineer job openings:

Deloitte rating
8.2
Based on 93 frontline employees who took The Breakroom Quiz
46th of 152 rated financial services
Job description
Work you'll do
As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk, and Forensic team, you will be responsible for...
- Lead end-to-end validation activities for GxP systems, including validation plans, IQ/OQ/PQ protocols, summary reports, user requirements specifications, functional specifications, design specifications, and traceability matrices
- Apply risk-based validation principles to assess system impact, classify validation requirements, and support compliance with GAMP 5, 21 CFR Part 11, and data integrity expectations
- Drive inspection readiness activities, including gap assessments, mock audits, validation package reviews, and support for regulatory inspections and responses
- Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks, closure documentation, and tracking of open compliance actions
- Validate AI/ML-enabled GxP systems and automation testing frameworks, including development of validation approaches for non-deterministic outputs and documentation of AI governance requirements
- Ability to work independently and collaborate as part of a team
- Effective written and verbal communication skills
- Meticulous attention to detail and quality of work product
- Ability to build and sustain professional relationships
- Ability to lead projects or workstreams
- Ability to manage and prioritize multiple tasks in a fast-paced and dynamic environment
- Strong interpersonal skills and professional demeanor
- Ability to meet deadlines
- Ability to provide clear guidance to others
Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory environment into defensible actions that strengthen, protect, and transform their organization. Join our team and use advanced data, AI, and emerging technologies with industry insights to help clients bring clarity from complexity and accelerate their path to value creation.
Qualifications
Required:
- Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical
- Experience leading validation deliverables for GxP systems, including IQ/OQ/PQ protocols, validation plans, summary reports, user requirements specifications, functional specifications, design specifications, and traceability matrices
- Experience applying 21 CFR Part 11, EU Annex 11, GAMP 5, and data integrity requirements, including Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available principles
- Experience managing CAPA lifecycle activities and supporting inspection readiness for Food and Drug Administration or European Medicines Agency audits
- Experience validating AI/ML-enabled systems, distinguishing deterministic and probabilistic tool behavior, and qualifying or validating automation testing frameworks
- Ability to travel 10%, on average, based on the work you do and the clients and industries/sectors you serve.
- Limited immigration sponsorship may be available.
- Experience supporting periodic review programs for validated systems and associated CAPA triggers
- Experience validating cloud or software as a service platforms, including Veeva, ServiceNow, or Salesforce in a GxP environment
- Experience working in Agile delivery environments with validation activities embedded in sprints
- Experience with AI governance processes, including AI use case tracking, model risk classification, and disclosure requirements for GxP systems
You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance.
Deloitte is committed to providing reasonable accommodations for people with disabilities. If you require a reasonable accommodation to participate in the recruiting process, please direct your inquiries to the Global Call Center (GCC) at USTalentCICInbox@deloitte.com.
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Benefits
At Deloitte, we know that great people make a great organization. We value our people and offer employees a broad range of benefits. Learn more about what working at Deloitte can mean for you.
Our people and culture
Our inclusive culture empowers our people to be who they are, contribute their unique perspectives, and make a difference individually and collectively. It enables us to leverage different ways of thinking, ideas, and perspectives, and bring more creativity and innovation to help solve our clients' most complex challenges. This makes Deloitte one of the most rewarding places to work.
Our purpose
Deloitte's purpose is to make an impact that matters for our people, clients, and communities. At Deloitte, purpose is synonymous with how we work every day. It defines who we are. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities. Learn more.
Professional development
From entry-level employees to senior leaders, we believe there's always room to learn. We offer opportunities to build new skills, take on leadership opportunities and connect and grow through mentorship. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.
As used in this posting, "Deloitte" means Deloitte Consulting LLP, a subsidiary of Deloitte LLP. Please see https://www.deloitte.com/us/about for a detailed description of the legal structure of Deloitte LLP and its subsidiaries.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law.
Requisition code: 360010
Job ID 360010
About Deloitte
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Industry
Finance and insurance and business management consulting
Company size
10,000+ Employees
Headquarters location
Orlando, FL, US