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An exciting opportunity has arisen for an experienced Validation Scheduler to join a successful and growing Pharmaceutical team in the South East. The Validation Technologist will work in supporting Pharmaceutical manufacturing, with respect to the scheduling and execution of validation activities
Main responsibilities will be to:
Manage and schedule validation and requalification activities for GMP facilities for the Facilities Validation Department.
Manage and deliver specific Validation Projects according to the business priorities, including work scheduling and supervision of junior members of staff and contractors…
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Analytical Development Scientist will be varied however the key duties and responsibilities are as following:
1.To assist in development, transfer and validation of methods to support site projects and provide technical support…
£50000 - £65000/annum
The breadth of technologies and markets our client serves involves working with most of the biggest and best semiconductor, consumer electronics, multimedia and App content developers and industry partners in the world.
This role is based in the informal environment of our comfortable and well-equipped office near Monmouthshire, initially working and interacting with a partner organisation based in Eastern Europe.
The role is to work on an Ensigma RPU…
Milton Keynes Village
Main purpose of the job:
The standard desktop project will implement a standard desktop environment
- Same Operating System for everybody (Windows 7)
- Same general machine configuration and setup
- Same security setup/configuration based on new ePO platform and Wensense
- Standard set of applications for all users - including O365 and Lync (IM only)
- All local applications being centrally managed/published
- All mailboxes migrated onto O365 in the cloud
- All user and PC accounts migrated to global domain
- Basic but harmonized end user support solution to ensure support readiness from day
£20000 - £22000/annum
Our office is based in the centre of Manchester and we’re looking for a Payments Processor to join the Finance team, reporting directly to the Financial Controller.
The role will involve administration support to the Financial Controller & Accounts Department, ensuring payment activities, production of sales…
Validation Specialist - Permanent - Berkshire
The purpose of this position is to contribute to the Validation team maintaining the site compliance for all GMP equipment, utilities, and facilities at the Site with specific responsibility for the compliance of all CSV systems.
Provide validation support and advice on capital projects
Prepare and execute validation protocols for a range of production, laboratory equipment, facilities and utilities
Provide support and guidance to departments within the organisation on validation issues
Ensure validation compliance is maintained in accordance with the site validation…
Our success is driven by being at the heart of the UK’s gaming community through delivering incredible games launches and fantastic exclusive events. We are always looking for great talent and you’ll need to show that you can be the best and be part of a team which strives to be at the heart of the gaming community and industry, delivering for customers, teams and…
VALIDATION TECHNOLOGIST- WILTSHIRE - c£26,000 - £34,000pa
A pharmaceutical manufacturing organisation is looking for a Validation Technologist at their site in Wiltshire on a permanent basis.
The core function of the Validation Technologist role is to ensure that the appropriate risk based validation activities meet the required regulatory expectations. The role involves the writing of validation protocols, execution of qualification activities and the writing of validation summary reports for equipment used within the Research laboratories. This can include Incubators, Fridge's, Freezers, HPLC, Systems and Autoclaves.
We are currently looking for a Validation Engineer to join a leading Pharmaceutical business based in the Kent area. As the Validation Engineer you will be responsible for identifying validation requirements for capital projects and modifications to existing validated APC, equipment, facilities and utilities in conjunction with the Validation Specialist / Site Validation Manager.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Engineer will be varied however the key duties and responsibilities are as following:
1. Provide leadership and coordination in support of Pharmaceutical / Chemical validation activities, with…
Validation Engineer required for a six month contract in Livingston, you will be responsible for ensuring that all equipment, software, process and product is validated
You will be responsible to manage and execute validation projects. Develop an effective master validation strategy with cross functional input. Create validation protocols and reports and other documentation. Review paperwork and validation results. Carry out validation impact assessments for current equipment and be involved in the validation requirements for new equipment and ensuring the that validation is completed by the user department. Assess when re validation…
One of our Pharmaceutical clients in the South East is looking for a Validation Engineer to join them on a contract basis for 6-12 months. This is a varied role and will involve the validation of Equipment, Processes and Utilities at their manufacturing site in the South East.
Candidates need to be ideally available within 2 weeks and should have the following skills and experience:
Degree level qualification in an Engineering or Scientific subject
Knowledge of Pharmaceutical manufacturing processes and equipment
Previous experience working in a GMP regulated environment
2-3 years validation experience covering…
Validation Engineer (Manufacturing)
£60,000 to £70,000 + Training, Progression, Pension.
Excellent opportunity on offer to join a rapidly expanding, specialist organisation; offering progression to senior roles and the chance to make a big impact on the success of the company.
Are you a validation engineer who has worked on a variety of projects within the software/computing industry? Do you have knowledge of serialisation?
Established in 2002, this company has evolved into an internationally recognised industry leader in Equipment System Integration and System Support. Working with mostly pharmaceutical, automation…
Supporting the validation and life-cycle maintenance of assigned site systems, process and equipment to ensure reliability in the supply chain and to support the Department, Site and company objectives. This will involve review, approval and audit of systems documentation.
Participate in provision of Validation Plans which support the site.
Review and approval of Validation activities on site.
Work with the existing Validation team to ensure consistent delivery of high level Validation support.
Ensure that all Validation is being carried out to the highest standards of compliance.Due to the high volumes of applications…
Job: Validation Engineer
Location: West Lothian, Scotland
Length and hours: 6 Months Mon-Friday 8am - 4.30pm. 4 day working will will be considered if you need to stay away.
My client is a rapidly expanding biotechnology company. They are seeking a validation engineer who is able to work on site for a contract period of 6 months. Extension beyond this is a possibility as you will be working on multiple projects. This role would primarily suit validation engineers with a hands-on equipment or facilities background. But my client would also consider process engineers with similar experience.
Skills and experience:
Validation Engineer - Pharmaceutical - North West - Contract
Our client is a leading Engineering and Design company within the life Science sector. At present they are seeking a Validation Engineer or a 6 month contract based at their client site in the North West, UK.
Candidates will have previous pharmaceutical project experience with a cGMP environment and will have experience of process and equipment/utilities validation. Candidates will be required to lead C&Q activities and work with the client on associated CQV projects. Candidates will generate and execute validation protocols, (IQ, OQ, PO) and will take a hands on approach…
Light Commercial Division Validator/ Administrator £18k Cambridge based
You will be helping to processr Engineers’ jobs through to invoicing: once the engineers have attended a job, and have input time taken, parts used, any further work necessary etc, the job record needs to be transformed into a legible and meaningful invoice for the customer.
• Use experience, judgement and creativity to validate and convert jobs for invoicing; ensuring timely progression to invoicing, capturing all chargeable activities Identifying and resolving, or escalating as appropriate, any issues which are causing delays.
• Liaise with engineers, controllers…
REF NO: 24246
JOB TITLE: Data Validator
SALARY: Circa £17,000 pa (Dependent on Skills)
Data Validator required, long term contract with a view to Permanent Positions for the right candidates.
Applicants must have a good working knowledge of Microsoft Office products and creation of excel spreadsheets.
• Liaise with outside agencies and other contract partners to ensure queries are dealt with effectively and efficiently.
• Support the creation and maintenance of a robust tracking system for services and operational packs information.
• Where rejections are identified…
REPORTS TO: Chief Engineer
MAIN PURPOSE OF JOB
To provide technical and validation support for site engineering activities.
Key activities include:
a) Development of detailed design specifications for new or modified Automated process control (APC)/ equipment / facilities / utilities to satisfy user requirements.
b) Generate and execute Design, Installation and Operational Qualification protocols and reports in accordance with Company policies and procedures.
c) Provide input to the project plans detailing all validation activities and timings.
d) Support user groups…
Utilities and Sterility Validation Technologist
The Facilities Validation department supports cGMP manufacturing activities and is responsible for ensuring compliance to the cGMP guidelines on Validation activities.
The purpose of this role is to take the lead to execute validation activities relating to Utilities and Sterilisation systems.
The post holder will be required to write, review and where appropriate approve validation reports prior to execution, followed by report generation. The scope of the work will involve the qualification of HVAC systems, Clean rooms, Compressed gasses, Wfi, Purified…
We currently have an exciting opportunity for a Utilities and Sterilisation Validation Technologist to join a leading company based in the Wiltshire area. As the Utilities and Sterilisation Validation Technologist you will join the Facilities Validation department which supports cGMP manufacturing activities and is responsible for ensuring compliance to the cGMP guidelines on Validation activities.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Utilities and Sterilisation Validation Technologist will be varied however the key duties and responsibilities are as following:
1. To take the lead to execute validation activities relating…
Computer Systems Validation specialist
An opportunity has arisen for a Validation Technologist to work in supporting bio-pharmaceutical manufacturing, GMP regulated activities with specific focus on CSV.
To lead and execute CSV validation activities of computerised systems and associated equipment in accordance with current regulatory requirements.
MAIN DUTIES AND RESPONSIBILITIES
Take the lead in CSV and compliance projects, manage and deliver specific Validation Projects according to the business priorities.
Write, review and approve validation documentation including protocols and reports…
VALIDATION TECHNOLOGIST - UTILITIES & STERILISATION- WILTSHIRE - c£26,000 - £34,000pa
A pharmaceutical manufacturing organisation is looking for a Validation Technologist (Utilities & Sterilisation) at their site in Wiltshire on a permanent basis.
The core function of the role is to take the lead to execute validation activities relating to Utilities and Sterilisation systems. This will involve coordination with Engineering , Production, QC and QA departments to ensure a timely delivery of the qualification report. The post holder may be expected to supervise contractor resource where appropriate with responsibility to ensure adequate…
Senior Validation Specialist - South Wales - Permanent
This is a fantastic opportunity to work for one of the biggest Pharmaceutical companies in the UK.
The purpose of the role is to lead and ensure the complete delivery of fully compliant qualification and validation of any equipment, software, facilities, cleaning processes and operational manufacturing processes on site via themselves and their team. To ensure the complete delivery of fully compliant Product Quality Review reports and any follow up.
The Senior Validation Specialist is also responsible for the hosting and management of Validation Contractors and any associated agency…
Job Title – Senior Validation Officer
Location - Haverhill, Suffolk (CB9 8PB)
Salary – £28,000 - £39,000
Job Profile –
Our client is a recognised leader within the pharmaceutical and biotechnology industry, specialising in the R&D and manufacture of therapeutics for rare diseases. This particular plant manufactures the active ingredients for a product which is used to treat patients on kidney dialysis. It is also involved in the process scale up and development of new synthetic molecules. The company are looking for a Senior Validation Officer to join their expanding team.
Job Role –
Duties will include:
• Providing validation…
Validation Engineer, Llanberis, Gwynedd
To be considered for the Validation Engineer, Llanberis, Gwynedd, we are seeking an enthusiastic individual who enjoys a challenge and thrives upon the challenges of Validation engineering. The vacancy involves working within Engineering as part of the Validation team, Validation Engineer will be responsible for Characterisation/Validation at the Llanberis facility.
For this Validation Engineer, Llanberis, Gwynedd you will be responsible for:
* Lead an appropriate team (assemble) for Characterisation/Validation activities.
* Write Protocols and reports for Characterisation/Validation activities…
Andrew Bolton at CK Engineers is currently working with an international Pharmaceutical organisation to recruit for several Qualification & Validation Engineers to be based from their manufacturing site in Cheshire on a full time basis, initially on a 12 - 15 month fixed term contract, with possibilities of extension or going permanent beyond.
As a Qualification & Validation Engineer, you will be responsible for:
- Running qualification & validation (IQ/OQ/PQ) of production equipment, processes and facilities across site.
- Coordinating & supervising deviation investigations and recommending actions to prevent recurrence.
Excellent opportunity to join a market leading Company who are investing heavily and expanding rapidly. The Company is part of a large group who turnover more than 10 billion Euros and the site in South Wales employs over 170 staff. The group has ambitious growth plans for the South Wales site.
Salary: £30,000 - £40,000 depending on experience
The Role: Process Validation Engineer / Validation Engineer
We are currently looking to recruit a process validation engineer to support the company's development and testing activities; initially working on a project related to the introduction of two new products and subsequently on general…
Face to Face Validation Supervisor
Are you an experienced supervisor with excellent communication and time management skills?
TNK UK is looking for a Face to Face Validation Supervisor to support our Validation Team Leader in the pursuit to deliver quality interviewer data. Experience in a market research or telephone centre environment would be advantageous.
As a Face to Face Validation Supervisor you will need to prepare workloads for the shifts and brief the team on specific job instructions. You will be the main point of contact for the team and as such the role requires a strong knowledge of…
Validation Manager – Pharmaceutical – Sussex - £35-45k
A well-organised, experienced Validation Expert is required to join a growing company with a great working environment. The Validation Specialist will be a key member of the Quality department and will bring a pragmatic approach along with a very high standard of work to this small and highly skilled team.
A rapidly expanding business with multiple business streams in the pharmaceutical sector
Innovative manufacturing processes
Investing in people and technology
UK based manufacturing business with niche sector expertise
Solid order book and loyal clients…
Medical Device Engineer- Product Development & Validation Engineer wanted on a permanent basis to join expanding medical device company based in London' '
My client is a leading medical diagnostics organisation based in London and they are currently looking for a Product development & Validation Engineer to join them on a permanent basis. If you are interested in learning more about the opportunity or would like to apply do so now via the website or call Joseph Tiffin on 0161 868 2214.
This role is to provide;
· Develop product specifications / drawings / quality plans in conjunction with NPD and project team.
· Creating and managing…