Tech Quality & Compliance Associate

WCG

United States

On-site

USD 52,000 - 82,000

Full time

6 days ago
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Benefits offered by this job

Health and financial protection
401(k) with company match
Flexible spending accounts
Career development opportunities
Paid time off

Job summary

WCG is seeking an Associate, Compliance & QA (Technology) to support the maintenance of compliance standards across WCG Technology Solutions. You will ensure regulatory alignment with QA processes and be part of a team driving GxP, 21 CFR Part 11, and GDPR/HIPAA compliance.

The role requires 2–4 years in quality/regulatory roles, strong communication and technical writing, and the ability to educate staff on standards.

Qualifications

  • Two to four years in a quality/regulatory compliance position supporting QA projects.
  • Knowledge of FDA, ICH guidelines and GCP as they apply to clinical studies.
  • Experience supporting sponsor audits of organizational processes and documentation.
  • Knowledge of 21 CFR Part 11 and Computerized System Validation.

Responsibilities

  • Develop, maintain, and enforce the Quality Management System standards.
  • Support quality goals, objectives, and process improvements.
  • Educate staff on quality standards and best practices.
  • Engage with staff to author and revise internal technology standards (IT/Software Policies, SOPs).
  • Support validation deliverables for system implementations and changes.
  • Contribute to internal audits and vendor qualification audits.
  • Assist external audits including preparation and findings resolution.

Skills

Regulatory knowledge
Communication skills
Technical writing
Multitasking
Training delivery

Education

Bachelor’s degree in a science/technical field

Tools

Validation software
Audit management tools

Job description

WCG is seeking an Associate, Compliance & QA (Technology) to support the maintenance of compliance standards across WCG Technology Solutions. You will ensure regulatory alignment with QA processes and be part of a team driving GxP, 21 CFR Part 11, and GDPR/HIPAA compliance.

The role requires 2–4 years in quality/regulatory roles, strong communication and technical writing, and the ability to educate staff on standards.

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