Regulatory Specialist
Job
OREGON EMPLOYMENT DEPARTMENT
Newberg, OR (In Person)
Part-Time
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Job Description
Job Listing ID:
4498267Job Title:
Regulatory Specialist Application Deadline:
Open Until FilledJob Location:
NewbergDate Posted:
05/23/2026Hours Worked Per Week:
Not Provided Shift:
Not Provided Duration of Job:
Either Full or Part Time, more than 6 months You may contact this employer directly. (Obtain the contact information to print or add to your jobs.)Job Summary:
Description Charlie Gilmur with Robert Half is looking for a Regulatory Specialist to help sustain regulatory compliance and quality system performance for medical device products in Newberg, Oregon. This role works across engineering, quality, document control, and customer-facing teams to keep submissions, technical records, and quality documentation accurate and inspection-ready. The ideal candidate brings strong knowledge of global medical device regulations and can manage regulatory activities throughout the product lifecycle while supporting audits, labeling review, and continuous improvement efforts.Responsibilities:
- Lead the preparation, organization, and upkeep of regulatory submissions and product files for domestic and international markets.
- Oversee product registration, licensing, and renewal activities, ensuring approval records remain current and traceable.
- Evaluate design or engineering changes to determine regulatory impact and identify when additional submissions or notifications are required.
- Partner with internal teams to review product labeling, instructions for use, and related documentation for compliance with applicable market requirements.
- Maintain quality system documents such as procedures, templates, and manuals so they remain aligned with current standards and business practices.
- Plan and perform internal audits, document observations, and follow corrective actions through to completion.
- Support external inspections and third-party audits by assembling required evidence and assisting with responses to findings.
- Monitor changes in global regulations and standards, assess operational impact, and communicate necessary updates to stakeholders.
- Contribute to post-market quality and regulatory activities, including complaint analysis, adverse event reporting support, and recall documentation when needed.
- Provide training and practical guidance to cross-functional teams on regulatory expectations, risk management, and quality system requirements.
Job Order:
03600-0013441962 Requirements- Bachelor's degree or equivalent relevant experience in the medical device manufacturing industry; extensive industry experience may be considered in place of a degree.
- Working knowledge of medical device regulatory frameworks across multiple regions, including U.S., Canadian, European, and other international markets.
- Experience preparing and maintaining regulatory documentation, technical files, registrations, and product compliance records.
- Familiarity with quality management system standards and risk management principles, including ISO 13485 and
ISO 14971.
- Ability to assess engineering changes, product development updates, and labeling revisions for regulatory significance.
- Experience participating in internal audits, external audits, or regulatory inspections within a regulated manufacturing environment.
- Strong document control, organization, and cross-functional communication skills.
- Proficiency supporting quality assurance and regulatory compliance activities for medical device or closely related regulated products.
- whenever you choose
- even on the go.
Job Classification:
Compliance Officers Access our statewide or regional occupation report for more information about wages, employment outlooks, skills, training programs, related occupations, and more. CompensationSalary:
Not Provided Job RequirementsExperience Required:
See Job SummaryEducation Required:
NoneMinimum Age:
N/A Gender:
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