Top 13 Sr engineer software validation Jobs in Bend Or

Sr Engineer Software Validation
Medline Industries —Redmond, OR
- $101,000 - $152,000 a year
- Full-time
- Microsoft Word
- Computer Science
- Engineering
- Health insurance
- 401(k)
Senior Validation Engineer
Serán BioScience —Bend, OR
- Full-time
- 8 years
- Bachelor's degree
- Conflict management
- Disability insurance
- Health insurance
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Strategic Innovation Engineer
AAON —Redmond, OR
- $147,258 - $220,887 a year
- Full-time
- Engineering
- Ability to lift 50 pounds
- Analysis skills
- Profit sharing
- Health savings account
Product Development Engineer
Suterra —Bend, OR
- Full-time
- Engineering
- Mid-level
- 3 years
- Paid holidays
- Health insurance
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Product Engineer
AAON —Redmond, OR
- $102,876 - $139,186 a year
- Full-time
- 5 years
- ERP systems
- Analysis skills
- Profit sharing
- Health savings account
Senior Healthcare Integration Consultant - EDI 834 & Eligibility
Proactive Logic Consulting Inc —United States
- $75 - $110 an hour
- Contract
- Remote
- System design
- HIPAA
- Java
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Senior Software Engineer
TaxPlanIQ —United States
- $100,000 - $140,000 a year
- Email
- Remote
- Background check
- System design
- Java
- Health insurance
- Dental insurance
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Sr Engineer Software Validation
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Job SummaryJob DescriptionJOB SUMMARY…
$101,000 - $152,000 a year

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Sr Engineer Software Validation

Medline Industries -
Redmond, OR

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Job Details

Full-time
$101,000 - $152,000 a year

Benefits

Health insurance
401(k)
Paid time off
Employee assistance program

Qualifications

Microsoft Word
Project reporting
Feature validation testing
Customer communication
Software engineering
Performance improvement leadership
GAMP
Quality records maintenance
Computer Science
Requirements design
Automation
Kanban
ISO standards
Engineering
Strategy Development (Quality assurance practices)
Bachelor's degree in business
Document control experience within manufacturing industry
Engineering process optimization
FDA 21 CFR Part 11
Compliance management implementation
Quality reports
Bachelor's degree in engineering
Quality risk management
Medical device manufacturing facility experience
System validation
Software development
Design controls
Biomedical regulatory compliance
Regulatory submissions
Managing projects

Full Job Description

Job SummaryJob DescriptionJOB SUMMARYDeliver leadership-level role in the development and execution of validation projects, ensuring customer and regulatory requirements are met in a timely and satisfactory manner.MAJOR RESPONSIBILITIES<ul><li>Evaluate systems and applications to properly design organized and efficient software, process, automation, cleaning, facility, and utility system related validations.</li><li>Ensure scope and complexity of validations are commensurate with risk including the design, development, and implementation of test strategy, plans, scripts, and test procedures to meet requirements.</li><li>Coordinate, Execute, and Report on validation plans for custom and off-the shelf software.</li><li>Manage multiple, concurrent validation projects, including gathering and understanding customer requirements and effectively communicating project status to keep customer informed and satisfied.</li><li>Document validation protocols and reports with professional and technical written communication skills.</li><li>Know, support, and conform to Medline policies and relevant governing procedures.</li><li>Maintain awareness to industry and regulatory environment, including FDA, GAMP, ISO.</li><li>Maintain organizational excellence, including document control, quality records, detail, and thoroughness.</li><li>Evaluate ways to streamline and improve efficiencies in software validation and associated processes.</li><li>Provide team support in all validation initiatives as requested.</li><li>Support development and upkeep of Divisional SOPs as related to software use.</li><li>Provide system design feedback to ensure compliance with regulatory and Medline standards throughout the software development life cycle.</li></ul>MINIMUM JOB REQUIREMENTSEducation: Bachelor’s degree in Engineering, Quality, Business, or Computer Science.Work Experience:<ul><li>5+ years of experience in Manufacturing, Quality or Engineering.</li><li>3+ years of experience in GAMP 5 related computerized system validations, including designing, authoring, executing, and coordinating.</li><li>Direct experience operating in a medical device QMS environment, including FDA 21 CFR Part 820, ISO 13485, ISO 14971, General Principals of Software Validation, Electronic Records/Signatures.</li><li>Additional Experience applying knowledge of standard concepts, practices, and procedures within software engineering.</li><li>Experience and skills in influencing, leading and directing individuals in multiple functional areas.</li><li>Experience with project management (for example: planning, organizing, and managing resources to bring about the successful completion of specific project goals and objectives).</li></ul>PREFERRED JOB REQUIREMENTSWork Experience:<ul><li>Experience in Manufacturing, Quality or Engineering including 4 major validation subjects (e.g. Computer, Equipment, Cleaning, Process, etc.).</li><li>Experience with the following: - QMS – ISO13485:2016 - 21 CFR 820 QSR, 21 CFR Part 11 Electronic Signature, 21 CFR 801 Labeling - GAMP Good Practice Guide: IT Infrastructure Control and Compliance (GAMP 5) - ISO / Customer / Regulator Audits - FDA Product and Establishment Registration - GS1 / GUDID Management - Quality Management System / Medical device environment experience.</li><li>Proficient in MS Word, Project, Excel.</li><li>Experience in people and process management.</li><li>Continuous improvement and Kanban related project experience</li></ul>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.The anticipated salary range for this position:$101,000.00 - $152,000.00 AnnualThe actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click <a target="_blank" href="https://urldefense.com/v3/__https:/digital.alight.com/medline__;!!DjNdo6avjEs!o-bxZ6fy_WNH13q2FLYYmUMb1U4cic3ioox3ulm5dkpyivWM09cd64RN8rHuDH5AQKNiwEzHU2VbVJht5ginULSy5aJGsA$">here</a>.We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page <a target="_blank" href="https://www.medline.com/about-us/belonging/">here</a>.Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

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sr engineer software validation jobs in bend or

Sr Engineer Software Validation

Senior Validation Engineer

Strategic Innovation Engineer

Product Development Engineer

Product Engineer

Senior Healthcare Integration Consultant - EDI 834 & Eligibility

Senior Software Engineer

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