Associate Quality Assurance Auditor

Charles River Laboratories, Inc.; Tranent; On-site; GBP 28,000; Full time

Job summary

A leading company in the life sciences sector is seeking a motivated Associate Quality Assurance Auditor for a 12-month fixed-term contract in Tranent. The role involves ensuring compliance with regulatory standards, conducting inspections, and advising scientific teams, offering a competitive salary and clear career progression.

Benefits

Private healthcare

Pension scheme

Employee discounts

Volunteer opportunities

Clear career progression

Qualifications

• Degree in Life Sciences or Chemistry-related subject required.
• Interest in scientific research with a commitment to quality.
• Ability to work autonomously and as part of a team.

Responsibilities

• Ensure compliance with GLP and GCP regulations.
• Conduct inspections and internal audits.
• Advise teams on quality and compliance matters.

Skills

Attention to detail

Effective communication

Organization

Interpersonal skills

Education

Degree in Life Sciences or Chemistry-related subject

Job description

For 70 years, Charles River employees have collaborated to assist in the discovery, development, and safe manufacture of new drug therapies. Joining our team means making a significant impact on global health and well-being. We welcome candidates from diverse backgrounds in life sciences, finance, IT, sales, or other areas, as your skills are vital to our work. We are committed to helping you develop a passionate and rewarding career.

Job Summary

We are seeking a motivated, driven, and enthusiastic graduate to join our Safety Assessment team in Tranent as an Associate Quality Assurance Auditor on a 12-month fixed-term contract.

You will be part of a dynamic and expanding QA team, one of the largest in the country, leading in our field. Your role will be pivotal in developing pharmaceuticals, veterinary products, and agrochemicals to combat infectious diseases. You will oversee the scientific work carried out by Charles River through independent assessments, engaging in various projects and processes.

What is the role?

1. Work within our busy Quality Assurance (QA) team to ensure compliance with international Good Laboratory Practice (GLP) and Good Clinical Practice regulations.
2. Apply your scientific background in a primarily office-based, non-laboratory role.
3. Interact with staff across all levels at our site and globally.
4. Conduct inspections of studies and processes in laboratories and facilities, with potential opportunities across Europe.

Responsibilities include:

1. Review study plans to ensure proper planning.
2. Inspect procedures across laboratories and animal facilities, overseeing the full scope of work.
3. Perform internal audits to verify compliance with regulatory and internal policies, ensuring accurate reporting of data.
4. Advise scientific teams and management on quality and compliance matters.

Candidate Requirements

1. Degree in Life Sciences or a Chemistry-related subject.
2. Interest in scientific research with a commitment to quality and customer care.
3. Attention to detail, patience, and determination to complete tasks to high standards within deadlines.
4. Ability to work autonomously and as part of a team in a fast-paced environment.
5. Effective communication, organization, and interpersonal skills, including checking scientific calculations for accuracy.

What we offer

• Clear career progression and structured training schemes.
• Competitive salary of £27,163.48 per annum.
• Private healthcare, pension scheme, employee discounts, and volunteer opportunities.
• Role is largely office-based with flexible arrangements discussed to meet business needs.
• Application requires a cover letter.

Additional Information

Closing date: 03 June 2025. The role is based in Tranent, with potential for European inspections. The starting salary is £27,163.48 per annum.