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Intern Validation Engineer Ii Jobs (NOW HIRING)

Alphatec Spine

Validation Engineer II

Carlsbad, CA · On-site

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

Alphatec Spine

Validation Engineer II

Carlsbad, CA · On-site

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

Alphatec Spine

Validation Engineer II

Carlsbad, CA · On-site

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

Intellectt INC

Validation Engineer II

Carlsbad, CA · On-site

Validation Engineer II Location: Carlsbad, CA Type: W2 Contract Industry: Medical Devices / Healthcare We are actively hiring a Validation Engineer II in the Medical Devices / Healthcare industry.

Alphatec Spine

Validation Engineer II

Carlsbad, CA

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

Intellectt INC

Validation Engineer II

Bothell, WA · On-site

Validation Engineer II (Onsite) Location: Bothell, WA Overview: We are looking for a CQV / Validation Engineer with 5-8 years of experience in GMP-regulated pharma/biotech environments. This role ...

BCforward

Validation Engineer II

Burlington, NC

$40/hr

Validation Engineer II 10/24/2016 - 10/1/2017 780 Plantation Drive, Burlington, NC 27215 United States $40/hr on W2 Qualifications: Bachelor's degree in a science or engineering related field OR an ...

ImmunityBio

Validation Engineer II

El Segundo, CA · On-site

The Validation Engineer II works on many phases/sub-tasks of projects of moderate complexity and working under general supervision or mostly independently with minimal supervision. Essential ...

NKW NantKwest Inc

Validation Engineer II

El Segundo, CA · On-site

$115K/yr

The Validation Engineer II works on many phases/sub-tasks of projects of moderate complexity and working under general supervision or mostly independently with minimal supervision. Essential ...

Replimune

Validation Engineer II

Framingham, MA · On-site

$137K - $177K/yr

Summary of The Validation Engineer II will work as part of a larger validation team to ensure the biotech facility equipment, utilities, instrumentation and computerized systems are qualified and ...

Lancesoft

Validation Engineer II

Carlsbad, CA · On-site

$30 - $32.47/hr

Validation Engineer II Location: Carlsbad, CA 92008 Duration: 6 Months Description: Main Purpose of the Role * Responsible for creating and implementing the Client Division validation program.

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Intern Validation Engineer Ii information

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How much do intern validation engineer ii jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for intern validation engineer ii in the United States is $19.31, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $20.91 per hour, depending on experience, location, and employer.

What is the difference between Intern Validation Engineer Ii vs Validation Engineer I?

AspectIntern Validation Engineer IiValidation Engineer I
CredentialsTypically pursuing or recently completed a relevant degree; internship experienceBachelor's degree in engineering, science, or related field; some entry-level experience
Work EnvironmentInternship setting, supervised, part-time or temporaryFull-time, professional engineering environment
ResponsibilitiesAssisting validation activities, learning procedures, supporting testingPerforming validation tests, analyzing data, supporting validation protocols

The main difference is that Intern Validation Engineer Ii is an entry-level, internship role focused on learning and supporting validation tasks, while Validation Engineer I is a full-time position with more independent responsibilities in validation processes.

What cities are hiring for Intern Validation Engineer Ii jobs? Cities with the most Intern Validation Engineer Ii job openings:
What are the most commonly searched types of Validation Engineer Ii jobs? The most popular types of Validation Engineer Ii jobs are:
What states have the most Intern Validation Engineer Ii jobs? States with the most job openings for Intern Validation Engineer Ii jobs include:
Intern Validation Engineer Ii jobs near you

Validation Engineer II

Alphatec Spine

Carlsbad, CA • On-site

Full-time

Re-posted 21 days ago

Job description

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes. The Validation Engineer II operates under limited supervision and collaborates closely with R&D, Software Engineering, Quality Engineering, Mechanical Engineering, Marketing, and Regulatory to deliver innovative products to market in accordance with FDA, ISO, and IEC standards.
The Validation Engineer II supports a broad range of software-enabled medical devices within a product suite that includes intraoperative neuromonitoring, surgical alignment, robotic navigation, and a cloud-based end-to-end platform, among others.
The ideal candidate has experience validating software-based medical devices as well as strong technical, troubleshooting, documentation, and communication skills, and the ability to work seamlessly with cross-functional teams.
Essential Duties and Responsibilities
  • Leads verification and validation activities for assigned projects, ensuring quality, timeline, and compliance expectations are met while working alongside cross-functional teams.
  • Defines verification strategies for new product development, authoring high-quality test plans and protocols.
  • Supports continuous improvement of V&V practices by identifying inefficiencies, implementing process improvements, and participating in cross-functional problem-solving.
  • Creates and reviews design control documentation, ensuring requirements, test plans and protocols, test reports, and traceability meet FDA and internal quality standards.
  • Designs, develops, and qualifies manual and automated system-level test methods.
  • Performs validation of non-medical-device software tools and supporting systems as required, ensuring appropriate rigor and documentation.
  • Supports risk management activities in accordance with ISO 14971 by contributing to hazard analysis, risk controls, and verification of risk mitigations.
  • Seeks guidance from and collaborates with senior validation engineers; may informally assist with onboarding or knowledge sharing for newer team members.
  • Maintains regular and consistent attendance at the primary worksite.
  • Other duties as assigned.

Requirements
The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Foundational understanding of FDA Quality System Regulations (21 CFR Part 820) & ISO 13485
  • Foundational understanding of IEC 62304 and IEC 60601 standards
  • Foundational understanding of ISO 14971 risk management requirements
  • Familiarity with defect tracking and test management tools (e.g., Jira, Polarion)
  • Working knowledge of test method qualification methods (Gage R&R, Attribute Agreement Analysis) and competency using desktop lab equipment (function generators, oscilloscopes, etc.)
  • Basic to working knowledge of probability and statistics concepts, and design of experiments (DoE)
  • Experience supporting Design History File (DHF) documentation and Change Order routing
  • Exposure to or experience supporting regulatory submissions such as 510(k)s
  • Demonstrated organizational and time-management skills to support cross-functional project activities
  • Ability to communicate technical concepts effectively with internal stakeholders and cross-functional team members
  • Detail-oriented, deadline-driven, and able to work collaboratively in a team environment

Education and Experience
  • Bachelor's or master's degree in biomedical engineering or related field
  • 2-8 years of experience in V&V or systems engineering for medical devices, or other regulated industries

CERTIFICATES, LICENSES, REGISTRATIONS
ASQ CSQE or CQE preferred.
Equal Employment Opportunity & Other Disclosures
ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws.
For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable).
At this time, ATEC Spine does not sponsor employment visas for this position. Candidates must be authorized to work in the United States without the need for current or future employer sponsorship.
Salary Range
Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate's qualifications, education, skill set, years of experience, and internal equity. $90,000 to $110,000 Full-Time Annual Salary
Please Note: The employer will not sponsor applicants for work visas for this position.

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