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- Responsible for running the report detailing the weekly check of effective documents and withdrawn/superseded documents and placing any new/updated ones and ensuring that all previous versions are destroyed.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
Inside ICONContent type
BlogsPublish date
05/08/2025
Summary
Standing Strong on Ovarian Cancer Day: ICON's Commitment to Advancing Care Ovarian cancer remains one of the most challenging gynaecologic malignancies, both in terms of detection and treatmen
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/07/2025
Summary
Patient Centricity in Clinical Research: What it is and Why it Matters In the past, clinical research was designed around the needs of sponsors, researchers, and regulatory bodies. Patients were of
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/05/2025
Summary
Navigating Regulatory Landscapes: Comparing FDA, EMA, & MHRA in Clinical Trials In clinical research, no matter how promising a new therapy may be, it will go nowhere without regulatory appro
Similar jobs at ICON
Salary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Pharmacovigilance Reporting Associate to join our diverse and dynamic team. As a Pharmacovigilance Reporting Associate at ICON, you will be responsible for the accurate and
Reference
JR130042
Expiry date
01/01/0001
Author
Olivia MolinaAuthor
Olivia MolinaSalary
Location
United States
Department
Clinical Trial Management
Location
United States
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 organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
Reference
2025-118971
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan HolmesSalary
Location
Johns Creek
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Johns Creek
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Other
Job Type
Permanent
Description
Step into the world’s largest and most comprehensive clinical research organization, where healthcare intelligence drives innovation and excellence. Be part of a team that's shaping the future of eye
Reference
2025-118910
Expiry date
01/01/0001
Author
Jamie PruittAuthor
Jamie PruittSalary
Location
United States
Department
Clinical Monitoring
Location
United States
Remote Working
Remote
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
2025-118411
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
United States
Department
Clinical Monitoring
Location
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119396
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
US, Blue Bell (ICON)
Location
Burlington
Blue Bell
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Programming
Job Type
Permanent
Description
We have an incredible opportunity for a Senior Statistical Programmer I to join ICON’s Full Service Early Phase team. The Senior Statistical Programmer I will assist the US and/or EU Early Phase Stati
Reference
JR130530
Expiry date
01/01/0001
Author
Tallulah PierreAuthor
Tallulah Pierre