{"@context":"https:/schema.org/","@type":"JobPosting","title":"QA Auditor - GLP

LabCorp; Eye; On-site; GBP 35,000 - 45,000; Full time

Job summary

A global life sciences company is seeking an experienced Quality Assurance Auditor to join their team in Eye, Suffolk. This role involves conducting audits, ensuring compliance with regulations, and supporting quality initiatives. The ideal candidate has a proven work history in a GLP or GCP environment and strong communication skills. This position offers a competitive salary and a comprehensive benefits package including health cover and pension.

Benefits

Competitive salary

Comprehensive benefits package

Career development opportunities

Flexible working

Qualifications

• Proven work history in a regulatory environment working to GLP or GCP.
• Excellent attention to detail in audits and inspections.
• Strong verbal and written communication skills.

Responsibilities

• Follow applicable policies and Standard Operating Procedures (SOPs).
• Conduct Protocol review, data and report audits, process inspections.
• Ensure Regulatory Compliance and Quality Assurance responsibilities.

Skills

Attention to detail

Organisational skills

Process improvement skills

Strong communication skills

Ability to work independently

Microsoft Office proficiency

Tools

Microsoft Outlook

Microsoft Word

SharePoint

Microsoft PowerPoint

Microsoft Excel

Job description

Overview

We are seeking an experienced Quality Assurance Auditor based at our site in Eye, Suffolk.

Responsibilities

• Follow applicable policies and Standard Operating Procedures (SOPs)
• Navigate to the regulations and able to read / understand specific regulations
• Conduct Protocol review, data and report audits, process inspections
• Explain the role of QA (sufficient for client audits)
• Establish relationships with local QA colleagues
• Retrieve data for client visits / regulatory inspections
• Ensure Regulatory Compliance and Quality Assurance (RC&QA) responsibilities, as indicated in applicable controlled documents, are followed
• Work with operational management to support Quality topics and / or working on projects with QA team on other sites
• Contribute to local Quality initiatives and process improvement initiatives aimed at improving compliance and / or efficiency of the local QA organization
• Create and / or re-write QA SOPs based on findings from local quality initiatives

Qualifications

• A proven work history in a regulatory environment working to GLP or GCP
• Excellent attention to detail paired with organisational and process improvement skills
• Ability to work independently and with others
• Strong verbal and written communication skills with the ability to provide clear feedback
• Experience using Microsoft Office packages to include Outlook, Word, SharePoint, PowerPoint and Excel
• Ability to remain flexible

About Labcorp

Labcorp is a leading global life sciences company. With a mission to improve health and improve lives, Labcorp delivers world-class diagnostic solutions, brings innovative medicines to patients faster and uses technology to improve the delivery of care. At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions - because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people\'s lives. Join us and see how you can embrace possibilities and change lives!

Benefits

• A competitive salary together with a comprehensive benefits package including health cover and pension
• Unsurpassed career development opportunities in a supportive and experienced team
• A culture of CARE with access to various employee resource groups and wellbeing programs
• Flexible working on completion of training