QA Complaint Associate at Eurofins

Posted in Other 9 days ago.

Location: Indianapolis, Indiana





Job Description:



Company Description



Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. Eurofins PSS gives our clients an insourcing solution for all of their analytical testing needs. Are you looking for the opportunity to use your skills in order to impact a team in a fast paced environment towards our ultimate goal of testing for a better life? We can provide you meaningful work in a highly supportive and collaborative environment where we invest in you because our people are our chemistry!



Job Description



  • Monitor, triage and assign complaints timely and appropriately.

  • Understand the devices to support investigations as defined in associated complaint procedures.

  • Perform and/or lead detailed complaint investigations.

  • Perform examinations on returned complaint samples as applicable.

  • Ensure timely completion of complaint investigations.

  • Supports ad hoc complaint requests when necessary.

  • Utilize Failure Modes and Effects Analysis (FMEA), as applicable.

  • Utilize non-routine software tools or business systems to complete complaint investigations.

  • Ensure compliance with Medical Device Reporting (MDR) and other regulatory reporting requirements.




Qualifications




Basic Minimum Qualifications:



  • Associate's degree in engineering, medical or life sciences

  • Strong written, oral and interpersonal skills

  • Strong technical writing skills

  • Strong attention to detail, time management, teamwork, and ability to multi-task

  • Ability to work in a dynamic and fast-paced environment


Experience Desired:



  • Previous experience with deviation and/or complaint investigation processes

  • Proficiency in Microsoft Office Suite, SAP, Trackwise, Stature, Darwin and Veeva Vault programs

  • Experience in Manufacturing QC, QA, Technical Services or Regulatory

  • Knowledge of cGMP's

  • Knowledge of global medical devices and combination product regulations (e.g., 21CFR820, 21CFR Part 4, Part 11, ISO 11608, Canadian MDR, EU Medical Devices Directive/Regulation, JPAl, TGA, ANVISA)




Additional Information



Position isfull-time, Monday - Friday.Candidates currently living within a commutable distance ofIndianapolis
, INare encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options.


  • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options

  • Life and disability insurance

  • 401(k) with company match

  • Paid vacation and holidays

#LI-EB1



Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.


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