Health & Safety Coordinator
About the role
This vacancy has now expired. Please click here to view live vacancies.
Position Summary:
To Organize and Coordinate all relevant technical tasks required to support the laboratory personnel in producing high quality results and adhering to quality standards. Including but not limited to: maintaining multiple technical documents for regulatory requirements, review of all quality documentation for compliance and ensuring compliance with health and safety regulations.
Job Responsibilities:
- The management of the PT process including the preparation and circulation of PT CAP folders on a monthly basis, maintaining the completed folders pending the CAP results, evaluating and grading the CAP results upon return, ensuring the PT's are signed off by the relevant personnel if satisfactory or, if unsatisfactory, returning the pack to the Lab for investigation.
- Ordering the CAP PT's on an annual basis following consultation with the various departments. Cancelling and ordering any PT's throughout the year while ensuring that the CAP activity menu is kept up the date.
- Responsible for the set up and ensuring compliance to the Alternative Assessment schedule on an annual basis and the safekeeping of these once completed and signed off by the relevant people.
- Responsible for ensuring that the Correlation schedule is adhered to for the year.
- Maintain the New Test Implementation Spreadsheet globally to ensure that all items are completed in order for a new test to be activated.
- Responsible for the Rees system administration including quarterly rota generation and submitting payroll forms for on call personnel. Troubleshooting any issues with Rees or co-ordinating/overseeing the call out of Rees engineers should any issues arise with the system. Training new Staff and responsible for ordering new probes as and when required.
- Ensuring the annual calibration schedule for timers, thermometers, centrifuges, microscopes, safety cabinets, microscopes and pipettes is adhered to and arranged throughout the year including the review, sign off and filing/maintenance of the paperwork associated with it.
- Perform temp mapping on all freezers and, refrigerators and incubators. Sign off on all the maintenance paperwork.
- Responsible for running the report detailing the weekly check of effective documents and withdrawn/superseded documents and placing any new/updated ones and ensuring that all previous versions are destroyed.
- Responsible for sign off of the archive box paperwork and for the on-site and off site archiving of lab paperwork and retrieval of raw data as and when required e,g, for an audit.
- Act as local Health and Safety Officer to ensure compliance with Health and Safety Legislation. Responsible for ensuring all Health and Safety documentation is up to date and that suitably trained Health and Safety representatives and fire wardens are available within the company
Job Qualifications:
- Minimum of 2 years working in a Laboratory and relevant QA experience as an analyst in preferably GCP, or alternately GMP or GLP setting.
- Ideally a qualification in Health and Safety but at least working knowledge relating to Health and Safety in the workplace and the legislation relating to it. Ensuring that the Health and Safety policy is updated and maintained as and when required keep up to date with new legislation and maintain a working knowledge of all Health and Safety authority legislation.
- Excellent communication skills both written and verbal, Excellent organisational skills.
- Knowledge of CAP, 21 CFR Part 11, ICH GCP required.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/07/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/04/2025
Summary
Cybersecurity in Clinical Data Management In clinical research, data is both a vital asset and a significant responsibility. As trials become increasingly digitised and decentralised, the protectio
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/03/2025
Summary
Finding the Specialisation for You Clinical research is a dynamic, multidisciplinary field that brings together scientific innovation, operational rigour and patient-centric thinking. While many
Similar jobs at ICON
Salary
Location
Croatia
Department
Clinical Monitoring
Location
Croatia
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate (CRA 2 or SrCRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120898
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz SternlichtSalary
Location
Italy
Department
Clinical Trial Management
Location
Italy
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
2025-120421
Expiry date
01/01/0001
Author
Mattia CarcangiuAuthor
Mattia CarcangiuSalary
Location
United States
Department
Clinical Monitoring
Location
United States
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119125
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
United States
Department
Clinical Monitoring
Location
United States
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120160
Expiry date
01/01/0001
Author
Kala MurphyAuthor
Kala MurphySalary
Location
United States
Department
Clinical Operations Roles
Location
United States
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Clinical Trial Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120039
Expiry date
01/01/0001
Author
Kala MurphyAuthor
Kala MurphySalary
Location
Zagreb
Department
Clinical Operations Roles
Location
Zagreb
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Senior CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120899
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz Sternlicht