Complaint Mgmt Spec 2

Duration                       : 12 Months 

Total Hours/week        : 40.00

Client: Medical Device Company

Job Category: Healthcare

Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)Max pay rate of $37.18/hour and a max bill rate of $47.23/hour.

Work hours: 8:30 – 5 M-F

Remote with some onsite as needed, Must be local

Must haves on the resume: Quality Complaint Handling Experience, Prior Medical Device Experience, Regulation Experience 13485 21 CFR820, Corrective Action/Preventative Action expertise, data analysis

The Specialist, Customer Complaints is responsible for the completion of all tasks associated with complaint management and processing of event reporting, including communication for regulatory compliance with medical device reporting for both domestic and international agency regulations.

Remote position – looking to interview and fill quickly.
 

Roles & Responsibilities

• Job responsibilities, not limited to:
• Collaborate with appropriate clinical, technical, and/or regulatory employees to determine product event status and MDR reportability
• Assures timeliness and compliance with all FDA regulations and standards related to the review of events/complaints for BD products
• Write and submit eMDR reports to the FDA and Health Canada in strict adherence with regulatory requirements and timelines.
• Coordinate, research, and prepare correspondence in response to FDA and global regulatory agencies requests for additional information
• Maintain complaint and MDR file documentation in accordance with regulatory requirements. Completes global complaint handling and adverse event reporting activities related to BD products
• Comply with the site Quality System.
• Performs other duties as assigned.

Experience Required

•  1 to 2 years’ experience in Quality, Regulatory or Complaint management is preferred. May consider equivalent combination of education and experience.

Skills & Certifications

Knowledge, Skills & Abilities

• Working knowledge of QA, Regulatory/Quality Compliance in a medical device industry.
• Attention to detail is essential.
• Able to utilize computers for development of reports and summary of project experience.
• Strong proficiency with MS Office tools to include Word, Excel, PowerPoint and Outlook.
• Prior work experience with TrackWise Complaint Handling System preferred.
• Prior experience filing eMDRs preferred.
• Ability to work on multiple projects with various disciplines are essential.
• Ability to multitask in an ever-changing environment.
• Position requires innovative/critical thinking, ability to solve problems and meet deadlines.
• Strong communication, organization, presentation, and writing skills.

Eligibilities & qualifications

Education & Experience

• Bachelor’s degree (chemistry, engineering, nursing, microbiology, materials science, biology, biochemistry)