Thermo Fisher
QA Auditor I
Athlone, Ireland
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Matched against 2.4M live jobs from 200,000+ employers in 200+ countries.
Tailor my resume for this job →Apply from your AI assistant
Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.
Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.
hirly's read of this role
- Role family
- Finance
- Seniority
- Mid level
- Country
- IE
- Work mode
- On-site / unstated
- First seen by hirly
- 2 Oct 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join us as Associate Quality Assurance Auditor - And play a crucial role in ensuring compliance and excellence in our clinical auditing processes.
- What You’ll Do:
- Conduct a variety of routine client, internal or GxP audits
- Assist or may conduct non-complex process audits
- Perform other types of QA audits or activities (e.g. database audits, clinical study report audits, sample results tables, facility audits, process improvement)
- Serve as a resource to operational departments on audit or quality assurance subject matter
- Assist in the preparation of audit findings and/or other related information
- Education and Experience:
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification; Associate degree and relevant experience is acceptable in lieu of bachelor’s degree
- Previous lab or QA experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 year).
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
- Knowledge, Skills and Abilities:
- Introductory knowledge of applicable GxP and appropriate regional regulations
- Working knowledge of Good Manufacturing Practice (GMP) requirements
- Working knowledge of SOPs and WPDs
- Previous experience working in a laboratory environment is preferred
- Strong oral and written communication skills (including appropriate use of medical and scientific terminology)
- Good attention to detail
- Able to work independently or in a team environment
- Good problem-solving abilities
- Good organizational and time management skills
- Basic computer skills and ability to learn and become proficient with appropriate software
- Proven flexibility and adaptability
- Valid driver's license and ability to qualify for and maintain a corporate credit card with sufficient credit line for business travel
- Working Conditions and Environment:
- Work is performed in an office/ laboratory and/or a clinical environment.
- Exposure to biological fluids with potential exposure to infectious organisms.
- Exposure to electrical office equipment.
- Personal protective equipment required such as protective eyewear, garments and gloves.
- Physical Requirements:
- Ability to work in an upright and /or stationary position for 6-8 hours per day.
- Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
- Frequent mobility required.
- Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
- Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
- Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
- Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
- Frequently interacts with others to obtain or relate information to diverse groups.
- Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
- Regular and consistent attendance.
- Why Join Us?
- When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthrough.
Similar jobs
- QA Auditor / InspectorPae · 6 LocationsFirst seen 4d ago
- QA AuditorSharpservices · AllentownFirst seen 6d ago
- QA AuditorMaersk · USPHF03 - Chesapeake - 3025 Bromay RoadFirst seen 6d ago
- QA Auditor -3rd ShiftCREATIVE FOOD INGREDIENTS INC · Perry, NYFirst seen 6d ago
- QA Auditor -1st ShiftCREATIVE FOOD INGREDIENTS INC · Perry, NYFirst seen 6d ago
Browse similar roles
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job