I'm currently recruiting for a thriving and prestigious manufacturing client in Blackpool who are looking for a Data Analyst for their Sales & Marketing department. My client, a well established and growing business, are looking for an experienced Data Analyst to focus on their product portfolio..... click apply for full job details

Sarah Farrow is recruiting for a lab team leader on behalf of an industry leading provider of services to the oil industry, to be based at their site in Aberdeen on a permanent basis. Our client is a multinational organisation, which is currently experiencing a period of growth. The company offer structured training and excellent opportunities for personal development and career progression. You will be responsible for day to day supervision and leadership to a team of laboratory staff. Your duties will include: - Ensuring that work is carried out in accordance with approved standards and customer requirements. - Training and mentoring junior staff - Assisting with the generation of quotations - Acting as first line maintenance for testing, calibration and troubleshooting of equipment - Raising non conformances and deviations In order to be considered for the position you should have experience of working in a UKAS accredited laboratory, ideally in a high throughput analytical environment. Experience of working in a supervisory position would be highly beneficial for this position, although not essential as training will be provided in the area of leadership and management. 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 DH42875 in all correspondence.

Quality Officer Clinical Research North West £24,500 - £26,500 My client is a major health resource and clinical researcher. They are now looking to bring on board a Quality Officer to assist the Head of Quality in ensuring the department operates to a high standard within the UKAS accredited environment. The Role: You will be contributing to the development, implementations and maintenance of the Quality and functions across all sites. The role will incorporate responsibilities including SOP development, CAPA's, change control and deviation management. Suitable applicants will have: Experience working in quality assurance to ISO 9001, 27001 and 17025 standards Worked with process mapping and planning as well as introducing new procedures Experience of internal auditing to ISO standards Experience identifying, analysing and resolving non-conformance issues Educated to degree level Previous clinical laboratory-based experience Experience using Q pulse software is desirable The Package: In return, my client offers the opportunity to work within a dynamic team on a permanent basis with a competitive salary package (dependent on experience).

Cubed Resourcing are working exclusively with a leading designer and manufacturer of special purpose machinery, supplying globally to multi million, blue chip customer base.This is an innovative and progressive business that has people at the heart of its business, offering a fantastic working culture and progression..... click apply for full job details

Key Responsibilities / Outputs Deputise for the named Responsible Person, including but not limited to: Review and release of returned products Review of temperature data Review and approval of major deviations Management of recalls Providing GDP storage declarations Oversee change control projects Review and approve company Quality Technical Agreements with clients and suppliers Day-to-day technical management of the departmental resources Plan, perform and follow-up on self-inspections and supplier audits allocated for completion Hosting of client/3rd party audits, and managing any non-conformances to satisfactory outcome Hosting client quality review meetings Develop and deliver Teammate training in quality aspects and GDP requirements Perform detailed root cause analysis on both internal and external non-conformances to ensure corrective measures can be implemented Perform proactive data trend analysis to identify key areas for improvement, and propose / implement actions to address trends. Carry out process reviews across the business to ensure most effective and compliant processes are adopted Review and approve quality documentation: SOP's, Work Instructions, and Forms, to ensure compliance with required standards and consistent structure and language are used Perform and facilitate risk assessments on GDP and quality processes Review and approve temperature qualification reports for all storage and transportation areas Assist with any Quality related issues and reasonable management requests Qualifications / Experience /Knowledge / skills required for the job Degree educated or equivalent in a science subject is desirable Minimum of 3 years' experience of working within a quality department certified to ISO9001 standard Experience within Pharmaceutical and/or Healthcare Industry desirable Trained and qualified Lead Auditor (BSI or IRCA registration desirable) Ability to present and communicate with clarity and confidence to a wide range of audiences Computer literate in Microsoft applications Able to work under pressure and meet strict deadlines Able to prioritise and complete work with minimal supervision Able to work within a dynamic team and complete individual tasks Enthusiastically drive vision and change within the business Ability to influence at all levels Role requires some off-site travel and overnight stays Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

Victoria Walker is recruiting for a Medical Device Lead Auditor to join a contract testing company in their medical devices business unit. This is a full time, permanent role and this person can be field based covering the whole of the UK. The Company: Our client is a global leader and innovator in inspection, verification, testing and certification services. Trusted all over the world, our client is a market leader because they put 100% passion, pride and innovation into everything they do. A vacancy has arisen for a Medical Device Lead Auditor to join the team within the business unit focusing on the manufacture of medical, precision and optical instruments, watches & clocks. This is a field based role, in which travel will be required 75% of the time - therefore candidates must hold a full driving license and be flexible regarding over night stays. This role reports into the Medical Device Auditor Team Leader. The Role: Your main duties will be: -Responsibility for planning and conducting audits against the manufacturing of medical devices, in accordance with ISO 13485, MDD 93/42/EEC, and MDSAP standards -Enabling the delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards -Conduct audits (either desk-based or on client's sites) in accordance with established procedures, maintaining a high standard of service delivery that ensures effective customer relationships -Conduct Technical File reviews specific for products being authorized -Complete specific projects in relation to medical device procedures, processes, systems and documentation -If required undertake reviews of packs and make certification decisions within target timescales and in line with company policies and accreditation/approval requirements -Project-manage auditing teams, as appropriate, to maximise efficiencies, enhance client satisfaction and ensure compliance with standards -Support business development activities as required (including follow up and/or referral of enquiries, sales visits, assistance at events, seminars, etc) to enable on-going growth of the business Your Background: The ideal candidate for this role will have: -excellent working knowledge of ISO 13485, MDD 93/42/EEC and their application -able to demonstrate good manufacturing and technical knowledge of electro-medical devices (active devices); and their relevant harmonized standards -experience of conducting MDSAP audits or standalone Technical file reviewer would also be advantageous. -Applicants are welcome from any on site qualified medical device lead auditors working for a notified body, or as a Technical File reviewer or as a mixture of both. -strong background in the medical device industry, including: -experience in a technical, quality or manufacturing role -experience in the application of the device in health care services with patients -experience in testing devices -experience in performance testing, evaluation studies or clinical trials of devices -must be able to demonstrate an excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques -Bachelor's degree or equivalent in a relevant technology or equivalent tertiary qualification, for one or several technologies used in the medical device sector The Benefits: -Field based role -Salary offered is £48,000 - £56,000 depending on experience -Bonus of up to 10% -Immediate Health Cover -Pension scheme -Company Car 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 CH42937 in all correspondence.

This well-established full service agency pride themselves by turning out great design for their varied client list. This is a small yet perfectly formed agency in Yorkshire who deliver brand stories. Job Description: Day to day you'll be working on projects from initial ideas to finished artwork..... click apply for full job details

Victoria Walker is recruiting for a Lead Auditor to join a contract testing company in their ISO13485 medical devices business unit. This is a full time, permanent role and this person can be field based covering the north. The Company: Our client is a global leader and innovator in inspection, verification, testing and certification services. Trusted all over the world, our client is a market leader because they put 100% passion, pride and innovation into everything they do. A vacancy has arisen for an ISO13485 Lead Auditor to join the team within the business unit focusing on the manufacture of medical, precision and optical instruments, watches & clocks. This is a field based role, in which travel will be required 75% of the time - therefore candidates must hold a full driving license and be flexible regarding over night stays. This role reports into the Product Operations Manager. The Role: Your main duties will be: -The successful candidate will be responsible for planning and conducting professional management system audits in accordance with the company's procedures to enable delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards. -Conduct audits (desk-based or on client's sites) in accordance with Medical Devices management systems standards ISO 13485. -Maintain a high standard of service delivery that ensures effective customer relationships and ongoing business development. -Complete all chargeable work within the required budget and timeframes to ensure customer satisfaction and efficiency of the business. -Ensure completion of all assigned work and relevant documentation in accordance with required procedures and standards to fulfil customer expectations -Provide accurate and timely reporting to assist the planning and management of operations. -Support business development activities as required (including follow up and/or referral of enquiries, sales visits, assistance at events, seminars, etc) to enable on-going growth of the business. -Manage personal schedule to work efficiently and to meet target chargeability requirements as defined by the Regional Manager. -Project-manage auditing teams, as appropriate, to maximise efficiencies, enhance client satisfaction and ensure compliance with standards. Your Background: The ideal candidate for this role will have: -A range of electro medical devices/ manufacturing experience, not just one -Full experience or responsibility of an ISO 13485 system and excellent working knowledge of ISO 13485 and its application. -A range of awareness of electrical components within the medical device industry -Work experience in positions with significant QA, Regulatory or management systems responsibility. -Knowledge of Risk Management EN ISO 14971:2012. -Able to demonstrate an excellent working knowledge of medical device management systems, standards and medical device compliance/auditing techniques. -Good knowledge of Design, manufacturing of medical devices, the technology involved and their intended uses. -Will be able demonstrate good manufacturing and technical knowledge of electro-medical devices and their relevant harmonized standards. -Please note this role will be field based and therefore candidates must hold a full driving license. The Benefits: -Field based role -Salary offered is £37,000 - £42,000 depending on experience -Bonus of up to 10% -Immediate Health Cover -Pension scheme -Company Car 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 CH42936 in all correspondence.

Senior / Principal Digital ASIC Design Engineer - Manchester £££Competitive package Based in Southern Manchester, our client is looking for a Senior or Principal level Digital ASIC Design Engineer to join them developing advanced satellite communications SoCs. It's a great chance to get to grips with complex ASIC..... click apply for full job details

Sarah Farrow at CK Science is recruiting for a Production Team Leader to join a leading manufacturer of laboratory instrumentation and consumables to be based at their site in Gateshead on a permanent basis. The Company: Our client is a well established manufacturing company, supplying their products worldwide. They offer excellent opportunities for career development and progression. Location: The site is easily commutable from across the North East of England, with good road links, based close to the A1. The area is well serviced by public transport. The Role: The main purpose of your role will be to manage a small team of staff involved in the manufacture of chemical products. Further responsibilities will include: - Ensuring that daily production targets and KPIs are met. - Planning staff resource levels and managing holidays. - Training staff, and addressing any skills gaps. - Driving improvements in quality, efficiency and delivery performance. - Development and maintenance of SOPs. - Overseeing departmental 5S activities. Your Background: To be considered for the position you should be an experienced supervisor or team leader, who has worked in a fast paced production environment. Experience of working in a chemical, pharmaceutical or related technical manufacturing environment would be highly beneficial for this position. 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 DH42941 in all correspondence

COVANCE is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries. We are currently recruiting for a Lead Scientist. The BioCMC solutions Division in York will accommodate: Protein Chemistry..... click apply for full job details

Senior Games Designer My client is one of the industry's leading games studios with some fantastic awards and titles under their belt. They are currently expanding their Design Team and looking for an experienced Senior Games Designer. What will you be doing? ..... click apply for full job details

A unique opportunity has arisen to join a small Birmingham-based laboratory, specialising in forensic toxicology. The company have an immediate requirement for an experienced LC-MS/MS Analyst to join the team. In this fast paced and dynamic role you will be responsible for providing a service to coroners, pathologists, hospitals and individuals in a UKAS regulated environment. You will undertake both qualitative and quantitative LC-MS/MS analyses for a wide range of drugs and intoxicants on body fluids and tissues. Applications are encouraged from accomplished LC-MS/MS analysts, ideally confident in both method development and validation. Previous forensic toxicology experience is preferred, although not essential. The role is offered on a temporary contract, rolling monthly, basis with a 36.5 hours working week. Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.

Design Coordinator Warrington, North West Salary & Package: £45,000 - £50,000, Car or Allowance, Bonus, 28 days hols + bank holidays Well known contractor are looking for candidates from either a civil engineering or architectural background and discipline who is looking for a change in role. The Company ..... click apply for full job details