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I am urgently seeking Validation Specialists for my Pharmaceutical client in the South.
They are an excellent company to work for, very pro-active with internal development and promotions, and actively cross-skill with departments. The team are friendly, supportive and approachable with a clear passion for what they do.
This role within the Validation team is necessary to manage and execute validation activities associated with the cGMP compliance of computerised and software systems, ensuring that they are appropriately qualified and fit for operational use.
The role will ensure that the commercial risks associated with…
£45000 - £55000/annum
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Analytical Development Manager will be varied however the key duties and responsibilities are as following:
1. You will take a lead role in the development and validation of analytical methods to support biopharmaceutical development activities. This will focus on HPLC and LC-MS methods for analysing protein and peptide products.
2. You will design analytical studies…
£30000 - £35000/annum
Process Engineer required by our specialist manufacturing client based in the North East. This role offers an exciting opportunity to work with an expanding business on a permanent basis.
• Preventative planned maintenance, fault finding and trouble shooting, problem diagnosis, repair (where possible) and ensuring adequate spares are in place to support business needs.
• Analysing machining problems, reporting and supporting improvements/solutions alongside continuous improvement of processes and operations machinery efficiency improvements
• To review and maintain adequate operating…
Leeds, West Yorkshire
Temporary – 1 year
Our client is a charitable housing association providing homes, care and support across Yorkshire.
They are currently seeking a Business Intelligence Coordinator to join their team based in Leeds for a one year fixed term contract. The main purpose of this role is to assist with developing and running the performance information systems to ensure that management has the correct information and intelligence to make effective decisions. Within this role your main responsibilities will include…
£35000 - £40000/annum
This is a full time permanent position starting ASAP, working hours are Monday to Friday 8am to 5pm.
As the Senior Sales Operations Analyst you will be the knowledge expert on specific portfolio of clients , responsible for the collection, analysis, business insight and reporting on key sales and providing valuable input into the business strategy and objectives/targets set by the business.
Other duties include:
- Report of key business metrics vs targets
- Weekly headcount validation vs plan and forecast…
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: Validation Specialist / Validation Specialist
We are currently looking to recruit a validation specialist 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 validation…
Biffa is the leading nationwide integrated waste management business providing collection, treatment, recycling and technologically-driven energy generation services. Through the expertise of our people and investment in technology we promote and deliver sustainable waste management solutions.
We are currently recruiting for a Data Analyst to be based at our High Wycombe Head Office.
Undertaking data analysis to produce quality / accurate MI for a variety of project and business stakeholders to an agreed timescale. Evaluate and monitor trends within the data to inform management and allow resources…
An exciting opportunity has arisen to join a world class project.
The purpose of the role is to work as part of the project management team to understand what HR services need to be provided to support project delivery and be the voice of the operational business in shaping those HR services.
What you'll be doing
Create and agree a People Plan with the Project Director, deliver against this and regularly report progress and issues. This will include:-
Resource plans for non-experienced (apprentice, grad and undergrad), experienced and contingent resource.
Training, development, talent and succession plans
We are currently recruiting for a Stock Analyst to work closely with the Senior Merchandising Manager to create and produces consistent weekly / monthly reporting for the business
Key areas of this role will include to:
Extract data from key systems within the business, reconcile and validate data to ensure accuracy
Distribute the reports/data to stakeholders within required timelines
Use this data to create a clear picture of current and future stock position, pro-actively highlighting future concerns
We're looking for someone who has the following experience/skills:
Strong Excel skills (Experience…
£18000 - £22000/annum
£18,000-£22,000 DoE / Days 37 hours / Permanent
The successful candidate will be required to design and prepare packaging samples through the creation of technical CAD drawings & request quotations from suppliers to assess cost in relation to the brief including the consideration of commercial and technical factors dependant on the product.
An exciting position with a real responsibility to meet client needs that will also require…
We are looking for an experienced Validation Officer for a bespoke pharmaceutical manufacturing unit based in West Yorkshire. The facility provides a wide range of high quality, affordable products including dermatological, oral and topical liquids, infusion fluids and ampoules. We also provide a bespoke packaging and labelling service.
The Validation Officer will work across the unit leading on validation and qualification activities. The successful candidate will be responsible for maintaining the Validation Master Plan, preparing and executing validation and qualification protocols, ensuring all validation activities undertaken meet…
VALIDATION SPECIALIST - SCOTLAND - 6 MONTHS - c£40 - £45 per hour
A leading pharmaceutical organisation in the Scotland is seeking a Validation Specialist to join their on an initial 6 month assignment.
The core function of the role will be to provide Validation support for new projects and retrospective Validation & Qualification of existing process equipment. The successful candidate will need to write and execute suitable documentation and Protocols including: IQ, OQ, PQ, DQ, URS etc. As well as Process / Manufacturing equipment, the Validation Engineer will also be required to work on Utilities, Facilities & Control Systems i.e…
One of our Pharmaceutical clients in the South East is looking for Validation Technologist to join them on a Permanent basis. 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 Equipment, Utilities and/or Processes…
This is an exciting opportunity with an established organisation specialising in providing services to pharmaceutical and biotechnology organisations world wide. Due to continued growth at their site in Glasgow, they're now looking for an experienced Validation Specialist to join their team. Reporting to the QA Manager, responsibilities will include:
Management of master validation plan and review of requirements for ongoing validation with quality assurance to ensure that production and activities are suitable supported
Responsible for provision, compilation and delivery of validation protocols or review of subcontractor protocols…
Validation Engineer - Sudbury
Our client is a supplier to the healthcare industry and is currently looking to recruit a Validation Engineer for a long term contract to work in Sudbury. You will ensure all systems are running according to necessary specifications and operate within regulations to ensure the production of quality products. Typical validation responsibilities include equipment budgeting, purchasing, monitoring and testing.
As Validation Engineer you will be responsible for:
*Coordination and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with…
My leading pharmaceutical client is currently looking for a Validation Manager.
The Manager is responsible for all Validation activities (equipment as well as processes) within our plant.
* To manage all operational validation activities within our organization.
* To maintain and continue improve a GMP compliant (EU and FDA) validation strategy and system.
* The scope includes:
* Equipment validation
* Utility validation
* Cleaning validation
* Computerized system validation
* Process validation (in collaboration with the client)
This includes the maintenance of the validation documentation system for these elements.
* To work closely…
The Just Recruitment Group Ltd are currently looking to recruit a Validation Engineer for our client based in Sudbury.
Successful candidates for the Validation Engineer will have a strong technical background, with an ability to communicate precisely and will have strong organisational skills and the ability to work under pressure. You will have 3 - 5 years validation experience within a pharmaceutical or medical devices manufacturing plant.
The position will include:
Coordination and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with policies
£50,000 - £55,000 per annum
We are currently recruiting for a Validation Engineer based in Cambridge, Cambridgeshire.
This is going to be a permanent position paying the successful candidate £50,000 - £55,000 per annum depending on qualifications and experience.
If successful you will be responsible for:
- Coordinating and implementing the validation programme for the new product
- This will include alignment of all Design Qualification, Verification/Test and Installation Qualification
- Working with project managers and integration teams to deliver the project/solution
My client is a major player in the pharmaceuticals market. They provide some of the biggest brands in both over-the-counter and clinical pharmaceutical products.
They have a long term opportunity for a validation engineer to join a well established team on a contract basis, lasting initially for 12 months.
The right validation engineer will need the following skills and experience:
* Degree qualified in Engineering based subject or related experience in a validation role.
* Experience within Biopharmaceutical Manufacturing environments with an understanding of Biologics manufacturing equipment and aseptic/sterile environments.
Our Client is an award winning network operator that specialises in delivering bespoke connectivity and cloud solutions exclusively to the wholesale marketplace.
Main purpose of the Role:
The Validation Managerwill control and place all orders with the carriers via the portal. They will be responsible for ensuring all orders taken from sales support are validated and checked. The Validation Manager will carry out necessary reporting to capture renewals and cessations and make reasonable recommendations to support the Head of Provisioning and Order Management.
Key Tasks and Accountabilities
•Raising of all new orders on the Carrier portals…
My client is seeking a multiple RTT Validator's (referral to treatment) to work on a contract basis within the NHS,
ROLE: RTT VALIDATIOR
CONTRACT: 2 MONTH
RATE: £100 PER DAY / £12.50 PER HOUR
This RTT Validator has the following skills / experience:
* Experience with RTT - referral to treatment validation
* Experience validating high volumes of records. eg 60 per day
* Experience working within an NHS / Hospital environment
* Experience performing duties of a Validation
* Experience using OMS - Oasis Pas System
If you feel you are suited to this role please send your updated CV.
Validation Specialist – Pharmaceutical manufacturing processes
Idyllic South Wales (Heads of the Valleys)
£30,000 - £40,000 (long contract will consider permanent).
My client has been manufacturing pharmaceutical products for over 20 years. In recent years their teams have rapidly expanded and they now formulate over 2,000 products. They have a diverse team of scientists who work on formulations, product development, regulatory support and analysis. Are you interested in a career working for one of Europe’s leading pharmaceutical manufactures?
The validation specialist will be part of a team of qualified scientists working alongside…
Working for a leading medical company on an initial 6 month contract, we are currently recruiting for 3 Validation Engineers.
The role will involve the development and supporting validation of:
- Programmable logic controllers PLC (e.g Allen Bradley, ELAU, Beckoff, Siemens, control logix etc)
- Bespoke Automation Equipment and software
- Control and instrumentation
- Vision systems (e.g Cognex and Insight)
- Configurable and bespoke equipment controls software (e.g SCADA, winCC, InTouch etc )
- Planning and execution of GRR.
- Creation/execution of qualification documentation
- Reviewing and authoring of technical documentation…
Validation Engineer (Pharmaceutical) Required- 12 month contract- Ireland
My Pharmaceutical client in Ireland are looking for a Validation Engineer to start as soon as possible.
The client requires a candidate with the following experience and expertise;
* General IQ, OQ, and PQ experience
* Experience working with Pharmaceutical equipment
* Be Comfortable with Pharmaceutical protocols
The client is offering;
* 12 month contract
* Immediate start date
* Market Rates
If you would like to be considered for this position please respond with an up to date CV. If you are not available but know of any friends / colleagues…
Validation Engineer- Pharmaceutical- Contract- South Coast
Our Client, a market leading Pharmaceutical Engineering consultancy is looking for a Validation Engineer, to start immediately on a 6month contract project on the South Coast. Candidates must have experience of aseptic filling lines, high speed powder filling lines, autoclaves, VHO hatches and have HVAC experience. Successful candidates will have a strong background in Validation Engineering, a can do attitude and be able to prepare, execute and write up protocols. Interviews will be immediate.
Established in 1978, NES Global Talent provides a complete range of contract…
Position: Senior Validation Specialist
Salary: £36,000- £42,000
An International Pharmaceutical Company based in Surrey are looking for a Senior Validation Specialist to join their team. They would lead the effective management of core quality validation processes and support activities in the Quality Assurance Department ensuring all goods manufactured and services provided by the Company meet cGMP and quality requirements of the Company, customers and regulatory authorities.
* Provide the leadership for the core validation processes in parallel with other stream leads to ensure effective…
Head of Validation (Modeller / Validation)
A respectable Retail and Commercial Bank is currently looking for a Head of Validation to be based in London. The Head of Model Validation will report directly to the Risk Management Director and lead the Bank's independent validation of Risk Models.
The Head of Model Validation will be responsible for leading the following activities:
- Ensuring effective independent validation of the Bank's Risk Models - Leading and managing the Model Validation Function
- Supporting effective implementation of Risk Model governance across the Bank in line with all regulatory requirements
A fantastic opportunity has become available for a Head of Validation to join a global Life Sciences business based in the Berkshire area.
As the Head of Validation you will be responsible for supporting all site validation activities concerning manufacturing, testing, engineering and CSV, ensuring compliance with GMP at all times. The Validation team is responsible for the management and execution of the Site Validation Master Plan, and qualifications regarding new projects for the site. The department also supports customer audits and Regulatory inspections.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Head of Validation will…
Analytical Method Validation Executive – Central London
This is a brand new opportunity that has been created due to expansion.
My client a leading pharmaceutical company is looking to recruit an Analytical Method Validation Executive where you will review process and analytical method validation status and reports against current standards and guidelines, highlighting any gaps and working with the relevant departments to develop remediation plans.
You will perform detailed validation gap analysis of process and analytical method validations (both chemical and biological) across a range of both sterile and non-sterile…
We are currently looking for a number of Validation Specialists with a CSV, Process, Facilities, Utilities or Equipment validation background to join a leading pharmaceutical company based in the South West. As the Validation Specialist you will be responsible for the generation, execution and review of all life cycle validation documentation for the qualification of processes, facilities, equipment and utilities.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Engineers will be varied however the key duties and responsibilities are as following:
1. Generate, execute and review all life cycle validation documentation…
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…
Senior Validation Officer
Our client, a manufacturer and developer of cosmetic and pharmaceutical products, have an exciting opportunity for a Senior Validation Officer to join their team at their North Herts based site.
Salary:£30k to £38k + benefits
All applicants must be UK or EU nationals or possess a valid visa to remain indefinitely.
*Degree level in a scientific or engineering field
*3 years Validation experience
*5 years in GMP environment
*Cleaning Validation experience
*Project management skills
*Site validation master plan and
Julie Marshall at CK Science is recruiting for a Validation Coordinator to join a company in the Berkshire region within the FMCG industry on a contract basis for 12 months.
The main purpose of the role will be to:
Work in multi-disciplinary teams across site to ensure that both existing and new equipment, processes and site systems are fully compliant with internal policy and procedures, as well as with EC Directives and Code of Federal Regulations.
Further responsibilities will include:
Ensuring all processes and equipment are validated in line with regulatory and company requirements.
Providing consistent validation advice and inform…