JUMP TO CONTENT

Health & Safety Coordinator

JR062224

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  • Responsible for running the report detailing the weekly check of effective documents and withdrawn/superseded documents and placing any new/updated ones and ensuring that all previous versions are destroyed.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.
List #1

Day in the life

Female in a lab environment
Good Clinical Practice (GCP) Fundamentals for Job Seekers

Teaser label

Industry

Content type

Blogs

Publish date

03/28/2025

Summary

 Understanding GCP Fundamentals The landscape of clinical research is continually expanding across the globe, playing a pivotal role in the development of innovative medical treatments and therapi

Teaser label

Learn the Good Clinical Practice (GCP) basics needed to excel in clinical research jobs.

Read more
Headshot of female
A Day in the Life of a Clinical Data Science Programmer

Teaser label

Our People

Content type

Blogs

Publish date

03/18/2025

Summary

    A Day in the Life of a Senior Lead Clinical Data Science Programmer In the ever-evolving world of clinical research, professionals with specialized technical skills play a crucial role in advan

Teaser label

Hear from Punitha how she advanced her clinical data science career at ICON.

Read more
Stethoscope and MS awareness ribbon
Multiple Sclerosis Awareness Week: Progress and Hope

Teaser label

Industry

Content type

Blogs

Publish date

03/13/2025

Summary

The Evolving Landscape of Multiple Sclerosis Research Multiple Sclerosis (MS) Awareness Week provides an opportunity to highlight the advancements being made in MS research and treatment. As an o

Teaser label

Discover how ICON researchers are advancing Multiple Sclerosis treatments through innovative clinical trials.

Read more
View all

Similar jobs at ICON

Global Clinical Development Leader (GCL) Neurology

Salary

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

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It

Reference

2025-117240

Expiry date

01/01/0001

Melissa Benner Read more Shortlist Save this role
Senior Pharmacovigilance Intelligence Specialist

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Mexico City

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Senior Pharmacovigilance Intelligence Specialist to join our diverse and dynamic team!As a Senior Pharmacovigilance Intelligence Specialist at ICON, you will be responsible

Reference

JR127117

Expiry date

01/01/0001

Florencia Pistolesi Read more Shortlist Save this role
In-House CRA/CTA

Salary

Location

Brazil

Department

Clinical Monitoring

Location

Brazil

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

The In-House CRA (IHCRA) performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in accordance

Reference

2025-118434

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Supervisor, Bioanalytical Services

Salary

Location

US, Lenexa KCIB (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Lenexa

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Bioanalytics

Job Type

Permanent

Description

We are currently seeking a Supervisor, Bioanalytical Services to join our diverse and dynamic team. As a Supervisor, Bioanalytical Services at ICON, you will oversee the daily operations of the bioana

Reference

JR129022

Expiry date

01/01/0001

Hanna Pitcairn Read more Shortlist Save this role
Manager, Sample Management

Salary

Location

US, New York, NY, Whitesboro

Department

Full Service - Development & Commercialisation Solutions

Location

Whitesboro

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Supplies

Job Type

Permanent

Description

We are currently seeking a Manager, Sample Management to join our diverse and dynamic team. As a Manager, Sample Management at ICON, you will oversee the collection, handling, storage, and distributio

Reference

JR128590

Expiry date

01/01/0001

Hanna Pitcairn Read more Shortlist Save this role
Lab Analyst II

Salary

Location

US, Lenexa KCIB (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Lenexa

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Laboratory Support

Job Type

Permanent

Description

We are currently seeking a Lab Analyst II to join our diverse and dynamic team. This position is for our Quality Control (QC) team with the LCMS department.As a lab analyst II (QC), you and your team

Reference

JR127603

Expiry date

01/01/0001

Hanna Pitcairn Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above