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- Analyst - Scientific
- Analytical Chemistry
A fantastic opportunity has arisen for a Cleaning and Process Validation Technologist to join a leading Life Sciences business who are based in the Wiltshire area.
KEY DUTIES AND RESPONSIBILITIES:
The Cleaning and Process Validation Technologist will be responsible for the following:-
1. Taking the lead to execute validation activities relating to Process and Cleaning validation. This will involve coordination with Engineering, Production, QC and QA departments to ensure a timely delivery of the qualification report.
2. The post holder will be expected to have a Hands-on approach to protocol execution with a can do attitude to service…
£20000 - £26000/annum
At ADP we are driven by your success. We engage your unique talents and perspectives. We welcome your ideas on how to do things differently and better. In your efforts to achieve, learn and grow, we support you all the way. If success motivates you, you belong at ADP.
£500 - £600/day
A Collibra SME is urgently required on-site at a Global Investment Bank on an initial 6 month contract to support the integration of a new Data Management tool - Collibra. You will also be developing Collibra meta data documentation.
The successful candidate must have previous Collibra experience as you will be the subject matter expert in the area.
Please apply if you meet the following criteria:
Previous experience implementing Collibra within Financial Services preferably
Strong Data Governance and Data Management skills
Previous experience developing Collibra meta data…
Validation Scientist, Perm, Livingston, £DOE
I am currently looking for an experienced Validation Scientist to join an expanding company based in Livingston. Reporting into the Validation Manager this role involves:
-Managing and developing validation systems
-Liasing with operational departments and learn about systems required by them (Production, QC, Facilities)
-Validation of new systems and revalidation of existing systems
-Working closely with QA to ensure all SOPs are current
Ideally you will have:
-Direct experience of validation within the pharmaceutical, medical device or biotechnology industry
£16 - £17/hour
Up to £16.66 per hour
My client, a global manufacturing leader based in Newcastle are is looking to recruit a Test Engineer with an immediate start. This is an opportunity jo join a market leading and global business for a minimum of 6 months.
• Create test strategy, test plan, perform test and data analysis related to new products before launch
• Prepare products for pre-submission for approvals
• Plan and direct technicians to build and validate new test equipment
• Support with product and test knowledge
• Build up personal network with international test houses
• Update test equipment…
The client currently has 4 other members in the team who is a pleasure to work with and is very passionate and dedicated to what they do. The office environment is very welcoming and the team encourages employees to achieve personal and professional goals as well as supporting the business goals. The two Directors are very hands on and strive to make sure…
A fantastic opportunity has arisen for a Validation Specialist. Our client is looking for an experienced validation specialist. As Validation Specialist you will also be responsible for:
•To compile and manage a Validation Master Plan for the Company, which is to include all revalidation requirements.
•Working with Process Development engineers, Quality Engineers, R&D and Operations personnel to generate appropriate IQ/OQ/PQ documentation.
•To ensure that the manufacturing/production facilities and associated process such as cleaning, sterilisation of product are validated as appropriate and in compliance with current regulatory…
£30000 - £38000/annum
As a Category Specialist, you will be working within a team of highly capable Category Managers and Specialists based in the Birmingham area. You will undertake strategic procurement in a range of allocated categories, providing best-value contract opportunities for a wide range of customers.
You will have the following responsibilities:
Delivery of allocated individual targets for savings, activity based income, contracted spend, savings validation
Develop high levels of category expertise
Management of allocated…
£23000 - £25000/annum
To organise & supervise the Analytical & Microbiological Laboratory team of around 10 technicians
Preparation of samples, equipment calibration, development, validation & review of analytical and microbiological test methods
Supervision, selection & training of all Technicians in accordance with procedures
Statistical analysis of complaints & queries including investigation & communication with other departments to identify root causes & future preventive actions, providing information as required
Nicholas Associates Engineering & Manufacturing are currently recruiting for a Validation Engineer. My client is a leading manufacturing business based in West Lothian who supply into the medical devices industry
Key responsibilities of the Validation Engineer role,
*To develop an effective master validation strategy for the company
*Ensure all equipment is consistently validated according to the applicable rules (EU, BRA, CHN and USA)
*Manage validation projects , executed either by internal staff or external contractors
*Develop validation plans within product development projects and VA1 ZEN - activities
* Prepare reports and presentations analysing financial results and financial reporting matters (including the interaction of accounting and actuarial data)
* Support the production of quarterly external financial reporting, half yearly results announcement and annual report and accounts. This includes project management of Group Finance deliverables, drafting wording to be included in the reports, calculation and validation of data and liaising with External Communications team
* Act as key liaison for the external auditors and coordinate the provision of key deliverables to assist…
We are GAME, the UK’s leading high-street videogames retailer, and pride ourselves on our people. With over 300 dedicated store teams across the country and a support and distribution centre filled with experts in their field, we know that are our teams are key to our success.
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…
Validation Engineer (Pharmaceutical Computer Systems – GAMP, FDA, GMP) – 12 month contract – Market Rates
Our client is a leading life sciences company with operations across the globe and as a result of growth and an increase in staff numbers they are looking to attract a Validation Engineer for Computer Systems on a contract basis for an initial 12 month period based at their facility in the West London area.
Candidates must have a GMP background in Validation within pharmaceutical or Biotechnology projects. Candidates must have experience of generating and executing protocols (IQ/OQ/PQ) and will ideally have experience of HVAC systems…
Validation Engineer - Contract - 6 months - North Wales
My client has a requirement for an experienced Validation Engineer for an initial 6 month contract. Please see below the relevant job specification.
Working within Engineering as part of the Validation team, Validation Engineer will be responsible for Characterisation/Validation at the Llanberis facility.
Essential Functions: (Limit yourself to 8-12 statements)
Lead an appropriate team (assemble) for Characterisation/Validation activities.
Write Protocols and reports for Characterisation/Validation activities.
Ensure Project/task completed in line…
Role title: Validation Engineer
Contract length: 3 months +
Working within Engineering as part of the Validation team, Validation Engineer will be responsible for Characterisation/Validation.
• Lead an appropriate team (assemble) for Characterisation/Validation activities.
• Write Protocols and reports for Characterisation/Validation activities.
• Ensure Project/task completed in line with business priorities.
• Lead risk assessment activities as required by the business.
• Support changes to either process or Test Methods in line with the Quality system
• Report any activities…
Validation Engineer – Midlands - £50-60k
Validation Engineer at a rapidly growing biopharmaceutical company.
The validation group is responsible for all aspects of validating our standard software platform including hotfixes, new releases, and customizations.
Responsibilities will include development of project specific offerings of standalone special purpose machinery for the biopharmaceutical sector.
+ Assist with writing, reviewing and executing customer FATs, SATs and IOQs for a highly customizable software package. Completed under the direction of the Validation Manager.
+ Assist with writing…
Austin Fraser are excited to be representing a world leading Pharmaceutical packaging supplier who work in close to 50 countries globally and are classed as one of the most innovative contract packaging services around the world.
The vacancy available is for a Validation Engineer to join their Quality and Engineering team on site and take responsibility for all Process and Equipment Validation activities on site in the South West of the UK, commutable from Oxford and Cheltenham. These responsibilities in the future have further scope to encompass the responsibilities for 2 sites dependant on the the level of experience…
EQUIPMENT & PROCESS VALIDATION / PROJECT ENGINEER - WEST SUSSEX - £40-50 per hour
A leading manufacturing organisation in the West Sussex area is seeking a Validation Engineer to join their team on an initial 6 months period.
Reporting to the Validation Manager the Validation / Project Engineer will help provide Engineering support to a major project for the business. Working with the Production, Quality and R&D departments to validate existing and new equipment, processes, data and documentation ready for the transfer of equipment to a new facility.
In order to be considered candidates must have experience preparing and completing…
Our Client is a large pharmaceutical manufacturing company with multiple sites in the UK and worldwide with an expanding portfolio of new products.
They are looking for a Validation Specialist to join the team in the North West to take a lead in performing the validation related activities associated with new product introduction and life cycle management.
The Main Duties of the role will be:-
-Prepare validation protocols to perform planned validation activities and write associated reports
-Organise work and coordinate co-workers support to meet deadlines for Industrialisation Group activities.
-To maintain the MSO process, cleaning…
Validation Technologist - Permanent - Cheshire
The purpose of the role is to design, execute, evaluate and report site thermal mapping qualification activities, including sterilization process qualification. To provide technical support during other manufacturing equipment and/or process qualification activities as required.
Key Results areas are:
To design, execute, evaluate and report thermal mapping qualification activities, ensuring adherence with current sterilization standards and regulations, and 'right first time' compliance with planned timelines.
To provide technical "hands-on" support in the areas of sterilization process…
Position: Validation Officer / Validation Engineer / Scientist
Salary: £24,000 - £34,000
Validation professional with a scientific/engineering background is needed to join a pharmaceutical company based in Wiltshire. The company are introducing a new product into their manufacturing lines and so they are in need of an individual with the knowledge of supporting procurement and installation of new equipment to GMP regulations.
Validation Officer / Validation Engineer / Scientist: Main Responsibilities:
- Understanding of equipment procurement and installation
- Liaising directly with suppliers…
Validation Engineer - Biopharma - Contract - South East
Our client is a leading life sciences company with operations across the globe. At present they are seeking a Validation Engineer on a contract basis for an initial 6 month period based at their facility in the South East, UK.
Candidates must have a GMP background in Validation within pharmaceutical or Biotechnology projects. Candidates must have experience of generating and executing protocols (IQ/OQ/PQ) and will ideally have experience of equipment qualification of bioreactors, autoclaves and cleaning validation.
Established in 1978, NES Global Talent provides a complete range…
A global Automotive supplier, who have recently secured additional work with a major OEM require a Validation Engineer on a 12 month contract basis. The company require two Validation Engineers on a 12 month rolling contract basis, based predominantly at their offices in Birmingham.
The overall purpose of this position will be to investigate proposals for cost, process and design improvement, then compiling and proposing test plans according to internal and customer specifications. You'll then be required to plan, co-ordinate and monitor test plans and programs before reporting back to Engineering and Plant teams across the UK.
REF NO: 24027
JOB TITLE: Digitiser/Validator
LOCATION: Sheffield, Yorkshire
SALARY: Circa 20,000
DURATION: 6 Months
Digistiser/Validator – Esri software preferable.
• Applicants will need to have excellent EXCEL skills and WORD, SAP or ESRI (ARCFM) knowledge is a distinct advantage. Applicants who are from a quantity surveying background, understanding design or digitising would be a distinct advantage.
• Work involves validation of project packs and documentation.
• Undertake redesigns to ensure that the design has been amended to enable digitisation to be done correctly and accurately.
• Uploading required…
The successful Validation Engineer will be responsible for ensuring that all manufacturing processes, packing operations, equipment, cleaning, utilities/facilities, computer and analytical methods are fully validated to meet the expected and operational requirements and GMP regulatory requirements.
Applicants must have the presence to promote the company image and ensure that this is enhanced by successful implementation of systems.
This will be an interesting and varied role, and the opportunity to progress within the team will be available to the right candidate. Appropriate training will be provide where required…
PM Group are seeking a Validation Engineer for an initial 6 month contract on a Pharmaceutical Site based on the South Coast.
To complete Validation Reviews on Equipment & Process Streams and documentation as required.
Ideally you will be degree qualified in a scientific or engineering discipline or have equivalent industry experience. API experience would be desirable but not essential.…
Quality Systems / Validation Specialist
C £35000 plus benefits
My Client, an expanding, major player in the Pharmaceutical Industry, is now looking to recruit a
Quality Systems Specialist to provide expertise and guidance to all user departments in the development of validation strategies and to ensure validation Inspection readiness.
The Role: Quality Systems / Validation Specialist
Ensures that all Quality System activities comply with the current Corrective and Preventive Action (CAPA) exception and Product Quality Review reporting processes
Review area project plans and identify validation requirements for a 1 to 2 year…
We are currently looking for a Validation Technical Specialist to join a leading biopharmaceutical company based in the Wrexham area. The main job duty for the Validation Technical Specialist is to take a lead in performing the validation related activities associated with new product introduction and life cycle management
KEY DUTIES AND RESPONSIBILITIES:
As the Validation Technical Specialist your main duties will be as follows.
1. Prepare validation protocols to perform planned validation activities and write associated reports as well as co ordinate co workers to meet deadlines.
2. To maintain the MSO process, cleaning and cold…
Andrew Bolton at CK Engineers is currently recruiting for a Calibration & Validation Technician to join a specialist Pharmaceutical organisation at their manufacturing site in Surrey on a full time, permanent basis.
As a Calibration & Validation Technician, you will be responsible for:
- Developing a maintenance programme to ensure all plant & laboratory equipment and site instrumentation are calibrated, qualified and were necessary validated appropriately.
- Producing SOPs for all calibration, qualification & validation activities to meet requirements.
- Ensuring all data is captured and recorded on the computerised maintenance management…
Based in Galway, Ireland the successful candidate will have experience in defining test strategy, designing and developing test cases from software requirements, architecture designs, and code of complex embedded real-time systems. Technical ability to understand the mechanical, electrical and software of the system is required. The successful candidate will have knowledge in C/C++/Java programming languages.
• Participating in the development and review of software requirements.
• Developing and reviewing software validation plans, test protocols, test data and test reports
• Executing test cases per protocol…
Cleaning Validation Specialist - Contract - South West, UK
Our client is looking for a contractor to provide services to support the validation of cleaning processes on existing equipment within the Manufacturing units located at our client site in the South West, UK.
Existing equipment includes:-
· Filtration Systems [Tangential Flow (TFF)]
· Filling Machines
· Freeze Dryers
· Washing Machines
· Associated Ancillary Equipment
The cleaning regimes of the above systems include manual and semi-automated / fully-automated (skid…
Controls Engineer (Validation)
£35,000 to £40,000 + 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 Controls engineer validation skills? Have you dealt with validation deliverables, with the ability to write and test scripts?
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, and medical…
Andrew Bolton at CK Engineers is currently recruiting for a Senior Validation Officer to join a leading Pharmaceutical Manufacturer at their site in Suffolk / Cambridgeshire region on a full time, permanent basis.
This role is based commutable from Suffolk, Cambridgeshire & Essex regions.
As a Senior Validation Officer, you will be responsible for:
- Leading validation & qualification (IQ/OQ/PQ) activities across the manufacturing site including coldchain projects, large-scale API manufacturing plant, production equipment, packaging & labelling equipment and automated control systems as well as processes.
- Running computer systems…
£20000 - £26000/annum
£500 - £600/day
£16 - £17/hour
£30000 - £38000/annum
£23000 - £25000/annum