DHR Reviewer I - Temp

The DHR Reviewer you will play a pivotal role in maintaining the integrity of our Quality systems and processes. You will be responsible for timely and accurate support of quality processes related to Device History Records (DHRs) to ensure compliance with Penumbra procedures and regulatory requirements. Hours for this role would be 8am-4:30pm.

Responsibilities

Review completed DHRs in accordance with internal procedure(s) with a high level of accuracy and attention to detail; Reconcile finished and rejected quantities; Verify training for personnel listed on DHRs; Communicate effectively with cross functional supervisors to correct any errors or omissions in DHRs or associated documents; Enter DHR information into relevant databases; Scan, label, and file DHRs; Assist with DHR records retrieval as requested; Demonstrate proficiency with Tier I level DHR Review

Requirements

A High school diploma and at least 2+ years of quality systems experience in regulated device or pharmaceutical environments, or equivalent combination of education and experience; High degree of accuracy and attention to detail; Proficiency with Microsoft Office (Word, Excel, Access, PowerPoint); Strong oral, written, and interpersonal communication skills

Nice to have

Proficiency with MasterControl preferred

Benefits

A collaborative teamwork environment where learning is constant, and performance is rewarded; The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases; A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s)