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Manager Quality Risk Jobs in Oregon (NOW HIRING)

Symbotic

Sr. Manager, Manufacturing Quality

OR · On-site +1

What we need As aSenior Manager, Manufacturing Qualityyou will create and communicateSymbotic ... Define opportunities for policy, process, and quality risk elimination activities acrosssupplychain.

Oregon Metro

Risk Manager

Portland, OR · On-site +1

$122K - $156K/yr

Supervise risk management staff and provide coaching, direction, and performance management ... of human qualities. Workplace diversity is both a moral imperative and a business strength ...

MANSCAPED

Director, Quality & Regulatory

OR · On-site +1

This role combines leadership in quality assurance, regulatory compliance, supplier quality, risk management, and continuous improvement The MANSCAPED Way - At MANSCAPED, what we do matters - but how ...

PeaceHealth

Clinical Risk Manager Sr

Springfield, OR · On-site

$105K - $158K/yr

Job Summary The Senior Clinical Risk Manager leads the investigation and management of complex ... In partnership with the Quality department, leads the organization's regulatory response in the ...

PeaceHealth

Clinical Risk Manager Sr

Springfield, OR · On-site

$105K - $158K/yr

PeaceHealth is seeking a Clinical Risk Manager Sr in Eugene Oregon for a Full Time, 1.00 FTE, Day ... In partnership with the Quality department, leads the organization's regulatory response in the ...

Talent ACQ

Quality Assurance Manager (Copy)

Woodburn, OR · On-site

$105K - $120K/yr

Quality Assurance Manager A high-volume food manufacturer is hiring a QA / Technical Services ... Trace and recall, CAPA, risk assessment, and non-conforming product decisions * Sanitation and GMP ...

SupportFinity™

Senior Project Manager I

Portland, OR · On-site

$150 - $200/hr

Maintain schedule and budget, manage quality, risk, safety, and compliance Qualifications * Bachelor's degree in Construction, Civil, or Architectural Engineering, Construction Management, or ...

Iberdrola

Senior Project Risk Manager

Portland, OR

Ensure the quality of risk management processes are maintained by auditing and verifying the metrics are continually aligned and updated, as necessary. Skills and Requirements * 3+ years of related ...

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Showing results 21-40

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Manager Quality Risk information

What is the difference between Manager Quality Risk vs Quality Assurance Manager?

AspectManager Quality RiskQuality Assurance Manager
Primary FocusIdentifying and mitigating quality risks across processesEnsuring products/services meet quality standards through testing and audits
CertificationsISO 9001, Six Sigma, Risk Management certificationsISO 9001, Six Sigma, Quality Management certifications
Work EnvironmentCross-departmental risk assessments, compliance teamsQuality labs, production lines, audit teams
Industry UsageManufacturing, healthcare, financeManufacturing, software, healthcare

While both roles focus on quality, the Manager Quality Risk primarily concentrates on identifying and managing potential risks to quality, whereas the Quality Assurance Manager ensures that products or services consistently meet quality standards through testing and process audits.

What does a Manager Quality Risk do?

A Manager of Quality Risk oversees the identification, assessment, and mitigation of risks related to product quality and compliance within an organization. They develop risk management strategies, ensure adherence to industry standards, and often utilize tools like risk assessment matrices and quality management systems. This role typically requires strong analytical skills, knowledge of regulatory requirements, and relevant certifications such as Six Sigma or ISO standards.

What cities in Oregon are hiring for Manager Quality Risk jobs?

Cities in Oregon with the most Manager Quality Risk job openings:

Manager Quality Risk jobs near you

Quality Assurance Senior Specialist

Bend, OR • On-site

Seran BioScience
Manufacturing • 1 - 10 employees
Learn more about Seran BioScienceexternal

$87K - $119K/yr

Full-time

PTO

Posted 8 days ago

Job description

Seran is seeking a Quality Assurance Senior Specialist who will be responsible for performing the day-to-day tasks of the QA Department supporting a GMP facility manufacturing, storing, and testing pharmaceutical products.  Primary responsibilities include overseeing Supplier Quality, Auditing (supporting regulatory and client audits, conducting internal and vendor audits), and managing the Quality Risk Management program.  Tasks include audit management, audit response, facilitating audit related continuous improvements, negotiating/processing Quality Agreements and continuous improvement.  Additional responsibilities include Quality Management System, risk analyses, change management and investigations/CAPA. 

Duties & Responsibilities
  • Performs internal and third-party audits. 
  • Supports regulatory inspections and client audits.  Manages and improves audit program.
  • Provides direction on audit operational activities and the development of audit responses, CAPA plans, and Effectiveness Checks.
  • Oversees company's supplier quality program including supplier qualification and audit (some travel required)
  • Assists in the oversight, facilitation, and implementation of continuous improvement of the company's quality systems 
  • Administers the quality risk management program and conducts risk assessments
  • Document authorship, review, and approval of SOPs, reports, and quality records.
Required Skills & Abilities
  • Knowledge of GMP and FDA regulations for drug manufacturing (21CFR 210-211). 
  • Knowledge of GMP, FDA, and EMA expectations for clinical trial and commercial materials, manufacturing, and testing
  • Excellent verbal and written communication skills
  • Excellent time management skills with a proven ability to meet deadlines
  • Excellent organizational skills and attention to detail
  • Demonstrated ability to collaborate and work in cross-functional teams
  • Scientific curiosity and willingness to learn
  • Strong analytical and problem-solving skills
  • Ability to prioritize tasks and to delegate them when appropriate
Education & Experience
  • Minimum of a Bachelor's Degree, preferably in a scientific discipline 
  • 8+ years previous quality assurance experience including Auditing and Supplier Quality experience 
  • Working knowledge of Veeva preferred
Physical Requirements
  • Prolonged periods of sitting at a desk and working on a computer
  • Must be able to lift up to 15 pounds

Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.

Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Benefits Summary:

Seran employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Seran covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees' wellbeing, along with access to pet insurance.

The Corporate Headquarters of Seran BioScience are located at 63047 Layton Ave, Bend, OR 97701

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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