Oxford Global Resources, LLC logo

Quality Systems Specialist I

Oxford Global Resources, LLC

MILWAUKEE, WIJob$63–83/hrSeen 4 days agoSeen in employer's feed 4 days ago

Most applications go out cold — see where you stand first. No sign-up to start.

Watch jobs like this.

At a glance

Compensation
$63–83/hr
Location
MILWAUKEE, WI
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

The Quality Systems Specialist I supports compliance, maintenance, and improvement of the global quality management system. The role assists with audit preparation, QMS documentation, procedure updates, change control, CAPA and NCR monitoring, and continuous improvement. It also provides compliance support across quality, regulatory, research and development, and operations functions, with work supporting a site based in Tucson, Arizona.

Skills & qualifications

RequiredNice to have

Skills

Quality Management SystemsAudit PreparationGap AnalysisQuality DocumentationChange ManagementCAPA ManagementInspectionAuditingContinuous Improvement

Qualifications

3 Years Related Experience5 Years Related ExperienceRegulated Industry ExperienceMedical Device ExperienceResearch Experience

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off

Full job description

JOB REQUIREMENTS: Number of Openings: 1 Job Title: Quality Systems Specialist I Occupational Category: Please choose the most appropriate choice based on the Job Title and Description. Duties and Responsibilties of Job: Summary: Supports compliance, maintenance and improvement of the global quality management system. Assists in all quality system activities. Supports development and implementation of Quality Management System (QMS) and supporting infrastructure/tools in compliance with FDA Quality System Regulation (QSR) regulations, International Standards Organization (ISO) regulations, and internal corporate requirements. Project Details: * Actively participate in audit preparation efforts for the site based in Tucson, Arizona by supporting planning, gap analysis, and mitigation implementation activities required to comply with new regulations and standards. * Responsible for supporting generation of QMS documentation using Electronic Document Management System (EDMS). Support coordination of document and record retention program for the site in alignment with the internal corporate requirements. * Write and revise Quality Systems procedures, perform gap assessments and assist in driving compliance. * Maintain processes/procedures to ensure compliance to internal and external requirements. * Provide compliance support for Quality Assurance, Regulatory Affairs, R&D, and Operations to assure regulatory compliance and appropriate business planning. * Create and monitors CAPAs and NCRs as required. * Assist manager in creating measurable data for periodic reviews of Quality System. * Provide support to carry out the creation, review, revision, approval, release and implementation of change orders within the Document Control System. * Initiate change orders and other required documentation in support of the Quality system process/records compliance. * Provide training support in quality concepts and tools. * Participate in and, where necessary, drive continuous improvement of the quality processes. * Support review of policies and procedures to ensure compliance with government regulations and international Quality System Regulations (QSR) including International Organization for Standardization (ISO) quality system standards. * Create internal audit reports and corrective action plans and establishes a structure to review audit findings and ensure effective remedial measures are agreed upon, implemented, and documented. * Miscellaneous duties including, but not limited to, supporting communications with scientific and regulatory bodies as necessary. Job Experience: * 3 years related experience in a regulated industry, 5 years preferred, preferably with Research * Experience in medical devices, or other regulated industry is preferred * Experience in Change Management, Inspection and CAPA Management is an added advantage. Exposure to internal, external, laboratory, supplier auditing programs as appropriate Hourly Rate: 63-83 Oxford is an Equal Employment Opportunity Employer. All qualified applications will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Oxford will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. Oxford provides supplemental medical (we do not offer major medical), dental, vision, life, and disability benefit plans along with a 401(k) Retirement Savings Plan. Paid holidays based on eligibility and paid sick leave for applicable jurisdiction, as required. Oxford is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please email oxfordbenefitsgroup@oxford orp.com. We will make a determination on your request for reasonable accommodation on a case-by-case basis. -- 3 Requirements -- ***** APPLICATION INSTRUCTIONS: Apply Online: https://www.aplitrak.com/?adid=YmJnZW5lcmljLjAxODM5Ljg3NzBAb25hc3NpZ25tZW50Y29tcC5hcGxpdHJhay5jb20 This position is listed by a private employment agency. The agency is the legal employer. No fee will be charged of the job applicant.

Similar jobs, posted recently

Open roles like this one, listed in the last 30 days.

You've read the whole posting — now see how you match it.