Parexel Hiring 2026 – Technology Quality & Compliance Opportunity
Are you looking for a career in pharmaceutical quality, GxP compliance, computerized system validation, or clinical technology?
Parexel is hiring for a quality-focused position within its Technology Quality & Compliance function. The role involves supporting quality systems, technology validation, risk management, audits, and compliance activities across clinical research and life sciences operations.
This opportunity is particularly suitable for professionals with 2–3 years of relevant experience in Computerized System Validation (CSV), Computer Software Assurance (CSA), GxP compliance, or clinical technology quality.
About Parexel
Parexel is a global Clinical Research Organization (CRO) that supports pharmaceutical and biotechnology companies throughout the drug development lifecycle.
Its services cover areas such as clinical development, regulatory operations, technology, quality, and other life sciences solutions.
For professionals interested in quality and compliance, Parexel provides exposure to global clinical research programs, regulated technology environments, and international quality standards.
Job Overview
- Company: Parexel
- Role: Technology Quality Specialist I / Quality Representative
- Department: Technology Quality & Compliance
- Experience: 2–3 years
- Qualification: Degree in Technology, Biological Science, Pharmacy, Healthcare, or related discipline
- Employment Type: Full-Time
- Industry: Clinical Research / Life Sciences
- Work Location: As specified in the official job posting
Note: The source listing describes the position as a Quality Representative within Technology Quality & Compliance. Candidates should verify the exact designation and location on the official Parexel careers page before applying.
Role Overview
The position focuses on maintaining and strengthening quality practices across technology solutions, computerized systems, clinical trial processes, and GxP-regulated activities.
The selected professional will work with internal teams and customers to support quality frameworks, validation activities, risk assessments, audits, quality issues, and regulatory compliance.
Key Skills Required
Candidates should ideally have knowledge or experience in:
- Computerized System Validation (CSV)
- Computer Software Assurance (CSA)
- GxP compliance
- GCP and clinical research processes
- GAMP 5 principles
- Technology validation
- Quality management systems
- Risk and impact assessments
- Audit and inspection support
- Change control
- CAPA and root-cause analysis
- SOP and policy development
- Project coordination
- Microsoft Office and Adobe Acrobat
Knowledge of AI-enabled applications and emerging technology validation practices can also be beneficial.
Eligibility Criteria
Candidates should have:
- A degree in Technology, Biological Sciences, Pharmacy, Healthcare, or a related discipline
- Around 2–3 years of relevant professional experience
- Experience in technology quality, CSV/CSA, GxP compliance, or clinical research
- Understanding of computerized systems used in regulated environments
- Good written and verbal communication skills
- Strong organizational and stakeholder-management abilities
- Ability to work independently while collaborating with global teams
Key Responsibilities
As a Technology Quality / Quality Representative, responsibilities may include:
- Support implementation and adoption of the company’s quality framework
- Provide quality guidance to project teams
- Support validation lifecycle activities for technology solutions
- Participate in risk and impact assessments
- Assist with supplier audits and vendor validation packages
- Manage quality issues and support CAPA investigations
- Participate in Change Control Board activities
- Support audit and inspection preparation
- Review SOPs, policies, and quality documentation
- Provide GxP-related guidance for technologies used in clinical trials
- Support regulatory and quality-related proposals or requests
- Maintain accurate administrative and project records
- Contribute to continuous improvement initiatives
Understanding the Technology Quality Role
This is not a conventional laboratory QA position.
Instead, the role sits at the intersection of technology, clinical research, quality systems, and regulatory compliance.
Professionals working in this area may deal with questions such as:
- Is a computerized system properly validated?
- Does a technology solution meet GxP requirements?
- Are appropriate risks documented and controlled?
- Are system changes properly assessed and approved?
- Is the required quality documentation complete?
- Are vendors and technology suppliers meeting quality expectations?
This makes the position particularly relevant for candidates interested in the growing field of digital quality and regulated technology.
Regulatory & Compliance Exposure
The role can provide exposure to major quality and regulatory concepts, including:
- FDA requirements
- European regulatory expectations
- ICH guidelines
- GxP requirements
- GAMP 5
- GCP
- Computerized System Validation
- Computer Software Assurance
- Quality risk management
- Audit and inspection readiness
Such experience can be valuable for professionals planning long-term careers in pharma quality, CSV, IT quality, clinical technology, or regulatory compliance.
Benefits & Career Growth
Depending on the applicable employment package, professionals can benefit from:
- Career growth within a global CRO
- Exposure to international clinical research projects
- Learning opportunities in CSV and CSA
- Experience with GxP technology compliance
- Exposure to quality audits and risk management
- Professional development opportunities
- Collaboration with global stakeholders
- Experience in emerging technology and AI-related quality considerations
How to Apply
Interested candidates should apply through the official Parexel careers portal.
Search for the relevant Technology Quality / Quality Representative position and carefully check the current job description, eligibility requirements, and location before submitting your application.
👉 Highlight relevant experience in:
- CSV / CSA
- GxP
- GAMP 5
- Clinical systems
- Technology validation
- Quality management
- Risk management
- Audit support
Important: Always apply through the official employer career portal and verify the job details before sharing personal information.
Is This a Walk-In Interview?
No.
This is an online application opportunity. The available listing does not provide walk-in interview details.
Why Consider Parexel?
A career in Technology Quality can open opportunities beyond traditional pharmaceutical QA.
Professionals can develop expertise across clinical technology, computerized system validation, GxP compliance, quality systems, audit management, and digital transformation.
For candidates who enjoy both technology and regulated life sciences environments, this can be a strong career direction.
Frequently Asked Questions
1. What is the experience requirement?
The role is intended for candidates with approximately 2–3 years of relevant experience in technology quality, CSV/CSA, GxP compliance, or clinical research.
2. What qualification is required?
A degree in technology, biological science, pharmacy, healthcare, or a related discipline is suitable.
3. Is this a laboratory QA job?
Not primarily. The position focuses on technology quality, validation, GxP compliance, risk management, and quality systems.
4. Is CSV experience useful for this position?
Yes. Experience in Computerized System Validation (CSV) or Computer Software Assurance (CSA) is highly relevant.
5. Is this a walk-in interview?
No. The opportunity is based on an online application process.
6. What regulatory standards are relevant?
The role involves concepts related to GxP, GCP, FDA, EU requirements, ICH guidelines, and GAMP 5.
7. Can pharmacy graduates apply?
Yes, candidates with a degree in Pharmacy or another relevant life sciences/healthcare discipline may be eligible, provided they meet the experience requirements.
