Premium Audit Reviewer
Location
United Kingdom
Posted
6 days ago
Salary
0
Seniority
Mid Level
Job Description
Premium Audit Reviewer
Davies
• Primary review of all premium audits (WC, GL, Garage, etc). • Audit types include: Phone, Mail, Physical, Remote Physical, Virtual • Independently determine if each audit adequately addresses the Afirm QC requirements, standard manual rules, state-specific rules, and client-specific requirements. • Validate time charges with audit detail and/or explanations. • Manage inventory of audits to review. • Meet production requirements and expectations as provided. • Other duties as assigned.
Job Requirements
- 2+ Years Premium Audit Experience
- Must have extensive knowledge of manual rules: Basic Manual, Commercial Lines Manual, State-Specific Manuals for independent bureau states
- Thorough experience regarding the usage of PAAS (Codes, Bulletins, FAQ’s, Chart of State Exceptions, etc)
- Proficient in both Workers’ Comp and General Liability audits.
- Knowledge of garage and auto liability audits is a plus.
- Must have strong computer skills.
- Knowledge of Microsoft Office, Power Point, Excel, etc.
- Must have excellent communication skills.
- Clearly and concisely identify errors and steps for resolution.
- Effective written communication with the auditors and other reviewers is key.
- Ability to work independently with minimal direction
- Highly motivated and detail-oriented with strong analytical skills
- Strong attention to detail and organization skills are necessary.
Benefits
- Flexible.
- Must have two (2) monitors for workflow efficiency.
Related Guides
Related Categories
Related Job Pages
More Reviewer Jobs
• Writing Indie Rock album reviews • Assigned roughly five articles per month • Consistency and adherence to deadlines
• Review audit packs to verify data and their content for compliance with MDD 93/42 EC or MDR (EU) 2017/745 • Verify that audit documentation for QMS on-site as well as technical documentation assessment complies with medical device regulations • Ensure that major non-conformity and any unsolved issues are addressed before transferring the audit pack for certification decision • Review whether the final review has been carried out by an approved Final Reviewer • Make the final decision as to whether a certificate should be issued • Check audit packs for QMS on-site audit for MDD / MDR / ISO13485 • Contribute to meeting operations objectives and Key Performance Indicators to deliver certificates to customers
• Review audit packs to verify data and their content for compliance with MDD 93/42 EC or MDR (EU) 2017/745 • Take decision on reviewed audit packs to determine if the certificate shall be issued • Verify that audit documentation for QMS on-site is in compliance with the medical device regulations • Review whether the final review has been carried out by an approved Final Reviewer • Ensure full compliance with the Company’s Code of Integrity & Professional Conduct • Report data on your daily workload and any technical issue.
• Review audit packs to verify data and their content for compliance with MDD 93/42 EC or MDR (EU) 2017/745 • Determine if the certificate shall be issued and if there is any applicable restrictions • Verify that audit documentation for QMS on-site and technical documentation assessment is in compliance with medical device regulations • Verify that all major non-conformity and any unsolved issue has been addressed and closed out • Review whether the final review has been carried out by an approved Final Reviewer • Ensure full compliance with the Company’s Code of Integrity & Professional Conduct • Reporting data on your daily workload and any technical issue
