CK Group are recruiting for a Principal Scientist to join a fast growing and leading global Contract Development and Manufacturing Organisation in the biopharmaceutical industry at their site in Billingham, on a full-time and permanent basis. Working as part of a team in a laboratory environment, your main responsibility will be to contribute to R&D DSP Operations acting as a Downstream Lead within a project team to provide high quality experimental planning and work in the development, evaluation and characterisation of processes for the production of novel therapeutic products (particularly proteins). Other key responsibilities include: - To identify, design, implement and manage DSP experimental development programmes needed to develop, evaluate and characterise new processes for target molecules. - To review experimental work, data and reports produced within R&D to ensure accuracy and compliance. - To assess manufacturing processes supplied by client companies for suitability for GMP manufacture and identify any scale-up requirements/issues. - To prepare reports and presentations for internal and external use in a suitable and professional manner. - To train and supervise the experimental work of other junior research staff. - To produce batch records for GMP manufacturing processes In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - A minimum of a relevant degree in a scientific discipline (Chemistry/Biological) or engineering. - 6 years relevant (protein purification) laboratory experience or Ph.D. - in-depth working knowledge of the key unit operations implemented in Downstream Process Operations e.g. buffer preparation and formulation, precipitation and clarification, refolding and solubilisation. - Awareness, understanding and experience working within a cGMP environment - Experience working with pilot-and /or largescale downstream processing operations This is an excellent opportunity to join the company during an exciting period of strategic growth offering structured training and progression opportunities. On top of this, you will benefit from their competitive salary plus company bonus scheme, 35 days of holiday, private healthcare and others. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47473 in all correspondence.

CK Group is recruiting for a Senior Stability Scientist to join a company in the pharmaceutical industry at their site based in Blackpool on a contract basis for 12 months and has an hourly rate of £29. The Company: Our client has one of the world's most comprehensive portfolios of orthopaedic and neuro products and services for joint reconstruction, trauma, spine, sports medicine, neuro, cranio-maxillofacial, power tools and biomaterials. The Location: Blackpool is a coastal resort on the Lancashire coast in North West England. The town is situated on the Irish Sea, 15 miles northwest of Preston, 27 miles north of Liverpool, 28 miles northwest of Bolton and 40 miles northwest of Manchester. Blackpool offers many attractions including Blackpool Tramway, Pleasure beach and Blackpool Tower. Blackpool can be reached via the M55 from the M6 and there are local bus services which run from Preston, Lancaster, Nelson, Southport and Fleetwood. The Role: To define and deliver technical justifications and shelf-life studies. Key Responsibilities: - Lead small scale manufacturing and laboratory technical projects. - Write technical justifications to provide evidence that stability studies meet requirements. - Write protocols and reports for shelf life studies. - Co-ordinate own week to week workload in line with your project plans and departmental priorities and overall business framework. Collate resource hours. - Develop intimate 'hands-on' knowledge of core business products. - Develop technical expertise in raw materials, in-process products and finished products. - Adhere to the Change Control and Design Control requirements. Your Background: - Degree qualified - ideally science. - Minimum of 2 years' experience in stability. - Previous experience in medical device or related regulated industry is essential. - Previous experience of project management and leading of small projects. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47468 in all correspondence.

Our Client is a leading beverages processing and distribution company who are currently seeking an experienced Technical Manager to be based at one of their key processing sites in Buckleys, West Yorkshire. The successful candidate will be required to possess a proactive approach towards ensuring that all Company and statutory requirements are compiled with in order to assure that products consistently meet the quality and legal specification required. This role is ideal for food safety and quality assurance senior professionals who hold an established history of consistently achieving BRC Grade A, managing detailed customer audits and carrying out relevant and periodic supplier audits. Experience of managing process documentation, QMS, compliance records, HACCP management etc is a key requirement, besides being accountable for managing teams including a laboratory function. Requirements: Management experience within an automated packaging and food production environment (essential) Experience of facing customer audits including major retailers, managing supplier relationship, liaising with appropriate statutory authorities (essential) Formal qualification in Food Technology (essential) Good IT skills and able to generating relevant management reports Proactive to drive continuous improvement, rigorous in problem solving Strong communication skills and excellent attention to detail Good organisational skills. Able to plan, prioritise and meet deadlines This is 5 days per week role, with an element of occasional travel to other Group sites

Have a background in Reg Affairs in Pharmaceuticals? Looking for a career move with a company that values it employees? Looking for a lift in your salary? The company: *Our client is a Pharma business, supplying a wide range of healthcare products into global markets. *Business growth combined with the organisations commitment to further reinforce its market leading status, has created an exciting opportunity for a contractor. The role: · Support regulatory submissions for approval to regulatory authorities worldwide. · Maintain current registrations, licenses, Regulatory Certification, and submissions to ensure compliance with the latest regulations. · Compile and maintain Technical Files. · Support other functions within the business for information requests, review of artwork and other literature · Review and approval of key compliance records (e.g. Labelling and instructions for use) for all sites. · Participate in company quality system, audits. The candidate: *Science or engineering based degree or equivalent qualification, experience of working in the Pharma industry would be an advantage. Ideally my client is looking for a self -driven individual, with strong communication skills. *Regulatory Affairs experience - minimum 1 years. *You must be authorised to work in the UK. Expion: Our healthcare manufacturing recruitment brand is well respected for the high quality of work we have delivered for both clients and candidates. Our in-depth knowledge of manufacturing recruitment across core sectors enables us to provide expert advice based on experience and to give you the best access to blue chip client vacancies. To apply for the role, please send your CV and salary details to Expion Search & Selection using the 'Apply Now' button. If you would like to have a confidential discussion on the role, you can contact the Consultant, Richard Clegg.

We are currently looking for a Clinical Data Manager to join a leading Contract Research Organisation based in the Cheshire area. As the Clinical Data Manager you will be responsible for all data management tasks for a programme of studies in clinical trials. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Clinical Data Manager will be varied however the key duties and responsibilities are as follows: 1. As Clinical Data Manager you will be responsible for developing the data tools and systems along with using clinical database applications to support database design and testing. 2. As a Data Manager you will contribute to the development of edit checks, protocols, plans and SOP's, identifying areas of process improvement where appropriate. 3. You will be responsible for monitoring data quality and integrity ensuring that GCP and regulatory guidelines are adhered to. 4. You will be required to generate data analysis status reports on clinical studies, and ensure that all modifications are communicated within the team effectively. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Clinical Data Manager we are looking to identify the following on your profile and past history: 1. Relevant BSc or MSc Statistics, Mathematics, Life Science subject or another related discipline. 2. Proven industry experience of data management and processes within pharmaceutical or clinical trial environment, ideally within Phase 1-3 of clinical trials. 3. A working knowledge of Electronic Data Capture (EDC) and practical expertise programming in JavaScript. Key Words: Data Management, EDC, JavaScript, Statistics, SOP's, GCP, Tools, Systems, Process Improvement, Data, Quality, Regulatory, CRO, Clinical Trials, Pharmaceuticals Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.

Position: Sensory Technologist Based: Littleborough Wednesday, Thursday, Friday 9:00am- 5:00pm Maternity cover for 14 months MAIN RESPONSIBILITIES Leading sensory panels, including sample collection & preparation Developing and/or implementing sensory evaluation procedures and methods Organising, designing, reporting on and interpreting sensory information at Littleborough according to recognised international guidelines, relevant & timely to meet business needs Providing sensory/technical support to improve McCormick business performance Maintaining sensory area, equipment and consumables to provide efficient working environment Executing routine sensory tests (including sample preparation, panel recruitment and data entry) in line with customer expectations and according to international standards Actively involved with the screening/training of new starters/potential panellists and ongoing calibration of panellists Managing the target selection programme Managing notice boards across the site Participating in investigations and studies to determine cause, effect & corrective actions as required to resolve deviation from quality standards Ensure full compliance with Company Quality, Food Safety Integrity, Health & Safety and Environmental requirements. CANDIDATE PROFILE Food engineering/ Biotechnology education background is seen as an asset but not mandatory Ability to prioritize tasks as well as to juggle them Good communication and cross-functional skills Excellent skills in tastes and smell identifying COMPANY At McCormick, we bring our passion for flavor to work each day. We encourage growth, respect everyone's contributions and do what's right for our business, our people, our communities and our planet. Join us on our quest to make every meal and moment better. Founded in Baltimore, MD in 1889 in a room and a cellar by 25-year-old Willoughby McCormick with three employees, McCormick is a global leader in flavour. With 11,000 employees around the world and more than $5 Billion in annual sales., the Company manufactures, markets and distributes spices, seasoning mixes, condiments and other flavourful products to the entire food industry, retail outlets, food manufactures, food service businesses and consumers While our global headquarters are in the Baltimore, Maryland, USA area, McCormick operates and serves customers from nearly 50 locations in 27 countries and 135 markets in Asia-Pacific, China, Europe, Middle East and Africa, and the Americas, including North, South and Central America with recognized brands. At McCormick, we have over a 100-year legacy based on our "Power of People" principle. This principle fosters an unusually dedicated workforce requiring a culture of respect, recognition, inclusion and collaboration based on the highest ethical values.

I'm currently recruiting for a leading supplier and developer of immunodiagnostic products, based in Birmingham, who are looking for a Technical Specialist to join their team. In the role of Technical Specialist you will provide a high level of scientific expertise on all of the company's product range and will be the go-to person for support for the wide variety of customers. This is an exciting and challenging role and will require the successful candidate to have exceptional ability to think quickly and be able to meet customer demands in an efficient manor, good time management and interpersonal skills are essential. To be the ideal applicant to this role you will ideally have experience of assay troubleshooting and will have worked in a laboratory setting previously and you will be degree educated (or equivalent). Any experience working in the IVD field would be advantageous and a UK drivers license is essential for the role. My client are offering an attractive salary package and a huge list of company benefits! To be considered for the role you will need unrestricted eligibility to work in the UK.

Excellent role on offer for an Ambitious Graduate looking for a role within a Market Leading, Multi-National company that will offer extensive training in their specialist industry. Do you have experience using CAD software and packages at College/University? Are you from a Civil/ Structural Engineering background?..... click apply for full job details

Design Draughtsperson Chesterfield - Derbyshire £35,000 - £40,000 + Training + Development + Bonus + Excellent Benefits Are you an experienced Design Draughtsperson with experience of Using AutoCAD 2D and 3D? Do you have experience of working on a range of projects involving wastewater, steelwork or pipework?..... click apply for full job details

Design Draughtsperson Chesterfield - Derbyshire £35,000 - £40,000 + Training + Development + Bonus + Excellent Benefits Are you an experienced Design Draughtsperson with experience of Using AutoCAD 2D and 3D? Do you have experience of working on a range of projects involving wastewater, steelwork or pipework?..... click apply for full job details

Due to our client winning high amounts of work for CP6 we are looking for a signalling principle designer. This is an excellent and exciting opportunity to join their signalling design office and work with one latest signalling equipment on the market, and be part of growing team with a great working ethos...... click apply for full job details

My client is one of the UK's leading consultancies specialising in telecoms and communications. Due to securing a major contract, their South Leeds office is urgently seeking to appoint a Senior CAD Technician to work in and help manage their existing team...... click apply for full job details

Our client are an award winning integrated agency that specialise in ideas. Big or small. Tactical or strategic. Ideas that not only capture peoples' imaginations but deliver on brand promise. You will be given the opportunity to work with some of the biggest retail brands in the world...... click apply for full job details

We are looking for a candidate with extensive experience working on the SQL Server Stack to our well-trusted client in Public Sector. The successful candidate will help develop information support into the business and will be able to identify opportunities to improve the quality and integrity of information flows covering a wide range of services...... click apply for full job details