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- Responsible for running the report detailing the weekly check of effective documents and withdrawn/superseded documents and placing any new/updated ones and ensuring that all previous versions are destroyed.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.
Explore more about ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
07/06/2026
Summary
Meet the CRA helping shape a new partnership Ask Rebeca Rojas Hernández what her dad tells people she does for a living and she can't help but smile. "He proudly tells everyone that I visit clinic
Teaser label
Our PeopleContent type
BlogsPublish date
07/06/2026
Summary
Inside the Role of a Senior CRA: Diego's Clinical Research Career at ICON Ask Diego Prieto what he does for a living and his answer is refreshingly simple. "I usually tell people I work on trial
Teaser label
Inside ICONContent type
BlogsPublish date
07/06/2026
Summary
Why returning to ICON was the right career move for Albert Bekfi Sometimes the next step in your career means moving on. Sometimes it means coming back. For Albert Bekfi, Vice President, Pharmacov
Similar jobs at ICON
Salary
Location
Singapore, Singapore
Location
Singapore
Kuala Lumpur
Remote Working
Remote or Office
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Project/ Program Management
Job Type
Permanent
Description
We are seeking an experienced (Senior) Translation Project Manager to lead the planning, coordination, and delivery of clinical document translations in a highly regulated global environment. This rol
Reference
JR155222
Expiry date
01/01/0001
Author
Sheni Krishnan
Author
Sheni KrishnanSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will
Reference
JR155935
Expiry date
01/01/0001
Author
Diego ToniniAuthor
Diego ToniniSalary
Location
Texas
Location
Texas
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:
Reference
JR155603
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
Chicago, IL
Location
Missouri
Michigan
Chicago, IL
Kansas City, MO
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:
Reference
JR155606
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
New York
Location
New York
New Jersey
Boston, MA
Philadelphia, PA
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:
Reference
JR155605
Expiry date
01/01/0001
Author
Brandon PupekAuthor
Brandon PupekSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.What You Will Do:Your role wi
Reference
JR153382
Expiry date
01/01/0001
Author
Simone ChanAuthor
Simone Chan