Jobs

Regulatory and Quality Coordinator


Job details
  • TEAM
  • Chertsey
  • 1 week ago

A successful subsidiary business of a large US-based multinational organisation is looking for a Regulatory and Quality Coordinator to join the team in the Midlands. They are a leading European based distributor of chemicals/products and have an exciting plan for expansion through growth and acquisition.  You will support and assist with UK Reach registration activities, the Quality Management system and manage the compliance and regulatory paperwork to ensure that the business is compliant and adheres to its obligations of Health and Safety.  As Regulatory and Quality Coordinator, your responsibilities will include:Review & management of Safety Data Sheets (Including Translations).Support with implementation of chemical notifications globally.Support with requests from internal business and external stakeholders.Support with UK REACH registration activities.Support & help manage the Quality Management system (QMS) to make and publish documented procedures available to all staff through thorough knowledge of ISO 9001: 2015 parent standard.Maintenance & upkeep of document control log and version history.Support in conducting internal audits and root cause analysis (RCA) of complaints.Support in writing of Quality / Regulatory monthly corporate & external reports as required.Job training shall be provided. Weekly catchups with Regulatory Compliance Manager to keep on top of project schedule and delivery.Support with H&S compliance impleme...

Sign up for our newsletter

The latest news, articles, and resources, sent to your inbox weekly.

Similar Jobs

Quality and Regulatory Coordinator

Proactive Personnel are currently searching for a Quality and Regulatory Coordinator for an international manufacturing company working in the food and beverage industry. This is a permanent full time position, our client is one of the largest manufacturers of fragrances, food colouring and flavourings working with some of the world’s...

Burton upon Trent

Regulatory Affairs Specialist UK & Ireland

Description Who we are At Kenvue , we realize the extraordinary power of everyday care.Built on over a century of heritage and rooted in science, we're the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnson's and BAND-AID® Brand Adhesive Bandages that you already know and love.Science is...

Kenvue Brands LLC High Wycombe

Senior Clinical Data Manager - single sponsor

Job Title:Senior Clinical Data Manager - single sponsorJob Location:Maidenhead SL6, UKJob Location Type:HybridJob Contract Type:Full-timeJob Seniority Level:Mid-Senior levelAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical...

Lifelancer Maidenhead

Biobank Manager

The Ellison Institute of Technology (EIT) Oxford’s purpose is to have a global impact by fundamentally reimagining the way science and technology translate into end-to-end solutions and delivering these solutions in programmes and platforms that respond to humanity’s most challenging problems. EIT Oxford will ensure scientific discoveries and pioneering science...

Ellison Institute of Technology Oxford

Clinical Study Lead (6 month project)

Oxford Global Resources is hiring a Clinical Study Lead (IVD experience is a must) for temporary maternity leave.As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols, investigator brochure, informed consent, contracts, and reports, in compliance with relevant...

Oxford Global Resources Liverpool

Clinical Study Lead (6 month project)

Oxford Global Resources is hiring a Clinical Study Lead (IVD experience is a must) for temporary maternity leave.As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols, investigator brochure, informed consent, contracts, and reports, in compliance with relevant...

Oxford Global Resources