QA Document Controller

Job Introduction **We are looking for**:A QA Document Controller to ensure the integrity of documentation, document control and systems to maintain GMP standards**At Pharmaron we offer**: - ** Vibrant and dynamic employment - **we are a highly specialised, growth company operating in a critical sector of the economy - our future is strong and exciting! - **...

We have an opportunity for a QA Supervisor to join a leading food manufacturer who supply to a range of retailers throughout the UK, based in Aintree, Liverpool. This is a full time, permanent role working Monday - Friday on a weekly rotating shift pattern 6am - 2pm / 2pm - 10pm on a salary of up to £25,000 per annum. Reporting into the QA Manager, You...

**Reference Number: JO-2311-525342** QA Associate Batch Release Rate: Negotiable **Job Type**: Contract Location: Liverpool QA Batch Release 12 month contract £19.45 per hour Liverpool Cpl Life Sciences are partnering with a global pharmaceutical company that focusses on developing life changing vaccines recruiting for a Quality Assurance Associate to...

Our client, a global leading consultancy, is currently seeking a dedicated and meticulous Document Controller to join the team. This is a unique opportunity to work with industry experts and contribute to high-profile projects while ensuring the delivery of compliant and traceable project documentation.Role Responsibilities:Provide document control for...

Document Controller 28,000 per annum Liverpool Full-time, Permanent We are seeking an experienced Document Controller to join an international subsea solution business from their HQ based in Liverpool. In this role you will manage documentation related to major projects, procurement, quality assurance and tenders for the business.Role Responsibilities...

A chance to progress your career with an amazing team - Competitive Salary **About Our Client**: The client is a well established company looking for a Document Controller to join their team! The Key Responsibilities: - Copy, scan and store documents - Check for accuracy and edit files, like contracts - Review and update technical documents (e.g. manuals...

We have an exciting opportunity for a highly organized and competent individual to join our team as an Office Manager / Document Controller. In this role, you will provide crucial administrative support to our Cambridge office and senior management team, as well as oversee office communications and coordinate events. Responsibilities will include managing...

**New** **Location**: *** **Liverpool** *** **Salary**: *** **Negotiable per hour** *** **Job Type**: **Temporary** Posted about 3 hours ago **Sector**: Construction **Contact**: Molly Briggs **Duration**: 31/12/23 **Start Date**: ASAP **Client**: Constructionline **Expiry Date**: 24 May 2023 **Job Ref**: MBR1/6653_1682329797 MBR1/6653 Document...

We are looking for: A QA Officer to be responsible for designing, implementing, and monitoring the QA systems for validation, GMP manufacturing, supplier management, quality control, batch review and release. At Pharmaron we offer: Vibrant and dynamic employment –  we are a highly specialised, growth company operating in a critical sector of the...

So you are a QA Technologist first and foremost? If yes then would working for a FTSE 100 company also appeal? If yes, then we are expanding our QA team here at B&M and we could have the ideal next move for you! **This role is full-time and permanent and based here at our Support Centre in Speke, Liverpool L24.** Reporting to the QA/Compliance Manager the...

The role of the QA Associate To provide first line QA support to the Liverpool site on a shift rotation. **1. **Batch Record Review. To work with other shift QA colleagues to ensure that all manufacturing batch records are reviewed in the specified timelines to assure compliance with the licenced and cGMP requirements. To provide quality advice and...

The role of the QA Associate To provide first line QA support to the Liverpool site on a shift rotation. 1. Batch Record Review. To work with other shift QA colleagues to ensure that all manufacturing batch records are reviewed in the specified timelines to assure compliance with the licenced and cGMP requirements. To provide quality advice and coaching...

**Automation QA- C#.NET - £60,000 - LIVERPOOL** Are you highly experienced experience with Automation, specifically in C#, ready for a new opportunity. I am on the lookout for two Automation Testers with over 3 years' experience in C#, Selenium and Specflow to join a world-class digital agency working for some of the world's biggest brands. They offer...

** Vibrant and dynamic employment - **we are a highly specialised, growth company operating in a critical sector of the economy - our future is strong and exciting! - ** Opportunities to develop your skills and yourself - **our rapid growth brings greater opportunities for you to learn and grow faster! - ** A great team where we all support each other -...

**Position Overview** Based at our site in Simonswood, on the border of Merseyside and Lancashire, Puratos are seeking a **QA Team Leader** to join our site team. This is a NEW role in our team; supervising 3 QA Technicians across 2 shifts. The role is full time working Monday to Friday, and you will need to be flexible to work on a rotating shift...

Title - Quality Assurance AssociateLocation: Speke, LiverpoolRate: Circa £19.18 p/hShift - M-F, 37.5 hrsContract - 6 months SRG is working on an excellent opportunity for a Quality Assurance Associate to join a global-leading pharmaceutical manufacturer working within the batch release team. This role would suit someone interested in moving into QA or...

Title - Quality Assurance Associate Location: Speke, Liverpool Rate: Circa £19.18 p/h Shift - M-F, 37.5 hrs Contract - 6 months SRG is working on an excellent opportunity for a Quality Assurance Associate to join a global-leading pharmaceutical manufacturer working within the batch release team. This role would suit someone interested in moving...

Batch Release Co-ordinator - £18.00 Based on Site in Liverpool. 12 Month Contract The role holder is responsible for working cross-functionally and reviewing and compiling batch specific documentation and data for batch release, ensuring compliance with licensed and cGMP requirements, escalation of potential issues, and timely submission of LRPs/release...

Company Overview: Join a leading pharmaceutical company dedicated to ensuring the highest standards of quality and compliance in the production of life-saving medicines. We are committed to delivering innovative therapies to patients worldwide and are seeking a passionate and experienced Quality Assurance Specialist to join our dynamic team. Position...

This is an exciting opportunity for a highly driven individual to participate in the development and delivery of the Radiopharmacy quality and clinical service from our state-of-the - art facility at Royal Liverpool University Hospital. The post-holder will be undertake quality assurance and quality control activities within the department as part of the...