LanceSoft Inc logo

Quality Engineer II - Exempt

LanceSoft Inc

  • Memphis, TN
  • 30+ days ago
  • $45–$50 Per Hour

Highlights

Join our dynamic team in Memphis, TN, a city known for its rich cultural heritage and vibrant community. Work with multiple software systems including Microsoft Office, Agile PLM, and SAP.

Numbers & Facts

LocationMemphis, TN
IndustryStaffing/Employment Agencies
Salary$45–$50 Per Hour
Company Size2,000 to 2,499 employees
Year Founded2000
Websitehttp://www.lancesoft.com/

Description

Join our dynamic team in Memphis, TN, a city known for its rich cultural heritage and vibrant community. We are seeking a dedicated professional to assist with the implementation of new projects in a manufacturing environment. This role provides an excellent opportunity to work closely with senior engineers, develop processes, and ensure the highest quality standards are met.

Must Have

  • 1-3 years of Medical Device industry experience
  • Familiarity with FDA 21 CFR Part 820 and EU 217/745 (EU MDR)
  • Knowledge of standards such as ISO 13485, ISO 14971, IEC 60601
  • Proficiency in Microsoft Office Applications (Word, Excel, Access, and PowerPoint) and Windows OS
  • Investigation and root cause analysis skills
  • Technical writing knowledge
  • Organization and communication skills
  • Process Validation and Computer software validation knowledge

Responsibilities

Responsibilities may include the following and other duties may be assigned:

  • Assist with the creation and revision of work instructions
  • Develop and execute validations
  • Analyze failures to create corrective actions
  • Revise pFMEA and work closely with Senior Engineers to develop processes
  • Train users in new processes and equipment validations
  • Work with multiple software systems including Microsoft Office, Agile PLM, and SAP
  • Design or specify inspection and testing mechanisms and equipment
  • Conduct quality assurance tests and perform statistical analysis
  • Ensure corrective measures meet acceptable reliability standards

Top 3 Technical Skills Required

  • 1-3 years of Medical Device industry experience, Familiarity with FDA 21 CFR Part 820, EU 217/745 (EU MDR), and standards such as ISO 13485, ISO 14971, IEC 60601
  • Investigation and root cause analysis skills
  • Process Validation, Equipment Validation, and Software/Spreadsheet validation knowledge

Education and Experience Required

  • Bachelor’s degree
  • 2-5 years of relevant experience

Additional Information

  • Work Schedule: 40 hours per week; 1st shift
  • Location: On-site in Memphis, TN
  • Interview Timeline: As soon as possible

About Company

We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc). 

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.

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