Quality Assurance Consultant

Oxford Global Resources, LLC

Arden Hills, MNFull-time$52–69/hrSeen todaySeen in employer's feed today

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At a glance

Compensation

$52–69/hr

Location

Arden Hills, MN

Schedule

Full-time

Work Authorization

Not specified

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Job overview

The Quality Assurance Consultant performs tactical quality work and reviews documents, protocols, and reports. The role covers documentation, review, and batch disposition for API and drug product used in Phase 1–3 clinical studies, as well as review and approval of manufacturing records, change controls, investigations, analytical data, test methods, method validations, and manufacturing validation protocols and reports.

Skills & qualifications

RequiredNice to have

Skills

Small Molecule ManufacturingContract ManufacturingCAPARoot Cause InvestigationProcess ValidationTest Method ValidationSoftware ValidationDesign ValidationEnvironmental MonitoringManufacturing OperationsVerbal CommunicationWritten CommunicationCollaborationAnalytical SkillsProject ManagementOrganizationQuality Manufacturing ProcessesSupply ChainInventory Management

Qualifications

Bachelor's in Engineering, Chemistry, Biology, or Related5+ Years Quality Organization Experience

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Match

Paid Time Off

Full job description

Job Duties

Summary:

Perform tactical work and review a variety of documents, protocols, and reports.

Project Details:

Exhibit varying levels of experience and a solid progression of work and/or training Document, review and batch disposition of API and drug product used in Phase 1-3 clinical studies Review and approve manufacturing records, change controls, investigations and analytical data Review and approve test methods and method validations Review manufacturing validation protocol and reports

Job Experience:

Experience in small molecule manufacturing and contract manufacturing Bachelor's degree in Engineering, Chemistry, Biology, or other related discipline A minimum of 5+ years' work experience in the Quality organization of a Medical Device and/or Pharmaceutical company Knowledge and experience in CAPA; Root Cause Investigation; Validation (Process, Test Method, Software, and Design); Environmental Monitoring, Manufacturing operation, etc. Excellent verbal and written communication skills Demonstrate ability to effectively collaborate and partner with all levels of management while maintaining an appropriate assertive style is critical Strong analytical skills Effective project management and organizational skills are essential Knowledge and understanding of quality Manufacturing processes and procedures, planning, supply chain, inventory management

Hourly Rate: 52-69

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 [email protected]. We will make a determination on your request for reasonable accommodation on a case-by-case basis.

Apply here: https://www.aplitrak.com/?adid=YmJnZW5lcmljLjgwNjIxLjEzNzk4QG9uYXNzaWdubWVudGNvbXAuYXBsaXRyYWsuY29t