Top 13 Sr validation engineer Jobs in Bend Or

Sr Engineer Software Validation
Medline Industries —Redmond, OR
- $101,000 - $152,000 a year
- Full-time
- Computer science
- 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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Senior Engineer, Process Development
Serán BioScience —Bend, OR
- Full-time
- Bachelor of Science
- 3 years
- Ability to lift 50 pounds
- Disability insurance
- Health insurance
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Senior Process Engineer, Spray Drying
Serán BioScience —Bend, OR
- Full-time
- Bachelor of Science
- Travel
- US work authorization
- Disability insurance
- Health insurance
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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 Salesforce Engineer
Brooksource —United States
- $65 - $75 an hour
- Full-time
- Remote
- Background check
- 5 years
- Senior level
- Health savings account
- Paid holidays
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Sr Engineer Software Validation
Medline Industries —Redmond, OR
Ensure scope and complexity of validations are commensurate with risk including the design, development, and implementation of test strategy, plans, scripts,…
$101,000 - $152,000 a year
Medical Laboratory Scientist or Technician
St. Charles Health System —Redmond, OR
Required: Bachelors, Masters or Doctoral degree in a chemical, physical, biological or clinical laboratory science from an accredited college or university.
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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

Project reporting
Feature validation testing
Customer communication
Computer science
Software engineering
Performance improvement leadership
GAMP
Quality records maintenance
Computer Science
Requirements design
Automation
Managing projects in an engineering role
Kanban
Team leadership
ISO standards
Engineering
IT quality control
Document control experience within engineering industry
Regulatory compliance
Bachelor's degree in business
Document control experience within manufacturing industry
Engineering process optimization
FDA 21 CFR Part 11
IT compliance audits
Quality assurance experience within IT
3 years
Compliance management implementation
Quality reports
Bachelor's degree in engineering
Quality risk management

Full Job Description

Job Summary

Job Description

JOB SUMMARY

Deliver 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

Evaluate systems and applications to properly design organized and efficient software, process, automation, cleaning, facility, and utility system related validations.
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.
Coordinate, Execute, and Report on validation plans for custom and off-the shelf software.
Manage multiple, concurrent validation projects, including gathering and understanding customer requirements and effectively communicating project status to keep customer informed and satisfied.
Document validation protocols and reports with professional and technical written communication skills.
Know, support, and conform to Medline policies and relevant governing procedures.
Maintain awareness to industry and regulatory environment, including FDA, GAMP, ISO.
Maintain organizational excellence, including document control, quality records, detail, and thoroughness.
Evaluate ways to streamline and improve efficiencies in software validation and associated processes.
Provide team support in all validation initiatives as requested.
Support development and upkeep of Divisional SOPs as related to software use.
Provide system design feedback to ensure compliance with regulatory and Medline standards throughout the software development life cycle.

MINIMUM JOB REQUIREMENTS

Education: Bachelor’s degree in Engineering, Quality, Business, or Computer Science.

Work Experience:

5+ years of experience in Manufacturing, Quality or Engineering.
3+ years of experience in GAMP 5 related computerized system validations, including designing, authoring, executing, and coordinating.
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.
Additional Experience applying knowledge of standard concepts, practices, and procedures within software engineering.
Experience and skills in influencing, leading and directing individuals in multiple functional areas.
Experience with project management (for example: planning, organizing, and managing resources to bring about the successful completion of specific project goals and objectives).

PREFERRED JOB REQUIREMENTS

Work Experience:

Experience in Manufacturing, Quality or Engineering including 4 major validation subjects (e.g. Computer, Equipment, Cleaning, Process, etc.).
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.
Proficient in MS Word, Project, Excel.
Experience in people and process management.
Continuous improvement and Kanban related project experience

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 Annual

The 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.

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 here .

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 validation engineer jobs in bend or

Sr Engineer Software Validation

Senior Validation Engineer

Senior Engineer, Process Development

Senior Process Engineer, Spray Drying

Senior Healthcare Integration Consultant - EDI 834 & Eligibility

Senior Salesforce Engineer

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