ISO 27001 Implementor/Auditor

at  IQVIA

zdalnie, województwo śląskie, Poland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate22 Apr, 2025Not Specified23 Jan, 20255 year(s) or abovePatient Outcomes,Commercialization,Database,Word Processing,Interpersonal Skills,Population HealthNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

JOB OVERVIEW

Plan and conduct independent audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines, policies, and procedures. Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies.

QUALIFICATIONS

  • Bachelor’s Degree Pref
  • 5 years experience in technical, or related area.
  • Knowledge of ISO 27000 family
  • Knowledge of word-processing, spreadsheet, and database applications..
  • Strong interpersonal skills..
  • Excellent problem solving, risk analysis and negotiation skills..
  • Strong training capabilities..
  • Effective organization, communication, and team orientation skills..
  • Ability to initiate assigned tasks and to work independently..
  • Ability to manage multiple projects..
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.
    IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.co

Responsibilities:

  • Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions
  • Support in large project; such as implementation of ISO standards in data centers
  • Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers
  • Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures
  • Provide consultation to customers and monitors in interpretation of audit observations and formulation of corrective action plans
  • Present educational programs and provide guidance to operational staff on technical procedures
  • Provide quality assurance consultancy activities and projects for clients within budget and established timelines
  • Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements
  • Host audits/inspections. Ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections
  • May perform GLP Archivist duties where needed
  • Manage/oversee quality events updates in eQMS and/or Maintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle


REQUIREMENT SUMMARY

Min:5.0Max:10.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

zdalnie, Poland