Quality Assurance Specialist – Cambridge
A growing Medical Devices company based in Cambridge is currently looking for a new Quality Assurance Specialist to assist in the development of the QMS system for ISO 13485 standards. They are open to candidates from alternative sectors, allowing for ISO 13485 standards training.
You will also be creating and managing technical files for several Medical Devices lines, including Class I, Class IIa and Class IIb Medical Devices. You’ll collaborate with a number of Medical Devices experts, but you will be the sole person focusing on Quality Assurance duties. However, you will receive Quality Assurance assistance from the parent company’s Quality Assurance Manager. Due to this, we are open to candidates who only have a couple of years of experience of ISO 9001 or QMS, but also keen to hear from people with more experience.
This is an excellent opportunity for someone a couple of years into their career and looking for more responsibility to lead the development of a QMS system, or for someone who is looking for a route into the Medical Devices sector under ISO 13485 standards. Due to the active work in setting up the QMS system, you will need to be in the office daily; however, over time there should be the opportunity for hybrid working.
It is expected that you would hold a degree in a subject that has led you into a Quality Assurance, Quality Engineering, or Design Assurance role.
Apart from having a Quality Assurance background, it would also be highly advantageous if you have a good understanding of Regulatory Affairs.
Part of your role will involve working alongside the manufacturing teams for these medical devices. Due to this, it would be highly beneficial if your Medical Devices Quality Assurance experience came from a Quality Engineering background, although this is not essential.
I anticipate a lot of interest in this role, so if you are interested, I suggest making an application now or risk missing out.
For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment, Science recruitment and Biotech recruitment specialists Newton Colmore Consulting, on +44 121 268 2240 or make an application and one of our team at Newton Colmore Consulting will contact you.....Read more...
Are you a Quality Assurance Manager - Manufacturing looking for an exciting job opportunity in Rayleigh, Essex?
My client is a top 5 manufacturer of PVC & Aluminium Windows and Doors in the UK. They are a massively growing company who are seeking a Quality Assurance Manager - Manufacturing to join the team. You will be responsible for inspecting procedures and outputs and identifying mistakes or non-conformity issues.
The Quality Assurance Manager - Manufacturing job based in Rayleigh responsibilities will include:
- Facilitate proactive solutions by collecting and analysing quality data
- Monitor all operations that affect quality
- Keep records of quality reports, statistical reviews, and relevant documentation
- Manage all aspects of organisations quality
- Ensure the auditing system is fit for purpose
The Quality Assurance Manager - Manufacturing Job will require the candidate to have:
- A Manufacturing environment background
- Solid experience in quality control is required for this role
- Motivation to learn and develop new skills
- Good knowledge of MS Office and ability to pick up new software easily
This is a great chance to join an established leading global company in Rayleigh, Essex, who offer outstanding career development and opportunities to work in a thriving and growing industry sector.
To apply for this Quality Assurance Manager - Manufacturing job based in Rayleigh, Essex please email Twilliams@redlinegroup.Com or call 01582 878821/ 07961 158764....Read more...
Are you looking to work for a global leading engineering business? Are you looking to develop and progress your career within a Quality Assurance Manager role?
If so, then our client has the job for you. This business, based in Bordon, Hampshire, is a global leader in the design& development of Military & Industrial Power products. They are currently recruiting for a Quality Assurance Manager Engineer to join their expanding R&D Electronics team.
In this Quality Assurance Manager job you will:
Develop and execute effective product quality plan to ensure design and product quality.
Data analysis of past problem history and warranty data to improve new product quality & reliability.
Active involvement in Design Failure Modes & Effects Analysis.
Responsible for acting as a liaison with external parties on all matters relating to Product Quality.
Provides leadership/mentoring and oversight to direct reports.
To apply for this Quality Assurance Manager job, based in Bordon, Hampshire, you will need a combination of the following:
Masters or bachelor’s degree in engineering or equivalent degree
10+ years of relevant experience in quality of consumer, automotive, medical and or electronics and electrical industry
Strong technical knowledge of electronic, mechanical, and electromechanical components, design and manufacturing
Demonstrated problem solving skills, using 8D, A3, DMAIC, SPC, DOE, PDCA, 5P, 5Why, FT, process mapping and/or equivalent quality tools, methods, and techniques
Excellent presentation, written and verbal communication skills
This is an exciting opportunity for an engineer to progress their career with a financially strong progressive mid-sized electronics company that is part of a global group.
To apply for this fantastic Quality Assurance Manager job please email LPhillips@redlinegroup.Com or call Lewis on 01582 878880 to talk about other Engineering jobs.....Read more...
Are you a Quality Assurance Manager – Compliance looking to work for an Internationally recognised business? If so, this could be the role for you….
Operating globally, and with their HQ in Surrey, my client develop temperature, pressure and flow instrumentation and measurement equipment for a variety of industries including Oil & Gas, Nuclear, Petro-chemical, Marine applications and Defence.
They are currently seeking a Quality Assurance Manager – Compliance, to maintain and continuously improve the Integrated Management System, covering Quality, EHS and Regulatory Compliance, throughout. In this exciting role you will support and improve on the effectiveness of key processes, internal audits, new product development and supplier performance.
Key skills and experience for the Quality Assurance Manager – Compliance, based in Surrey:
Relevant experience within a Quality Assurance / Compliance role
Relevant industry background – technology based for mechanical, electrical, electronic, instrumentation etc product development
Experience of Environmental, Health and Safety
Experience of Continuous Improvement
Experience of ISO9001 and be a lead auditor
This is a fantastic opportunity for the right person who is looking for the chance of career progression and personal development.
To apply for Quality Assurance Manager – Compliance, based in Surrey, please send your CV to skhuttan@redlinegroup.Com, or for more information contact Sophie Khuttan on 01582 878817 or 07961158586.....Read more...
A North London based Local Authority is looking for a Quality Assurance Auditor to assure quality of practice across children’s Social Care services. As the Auditor, you will be providing a proactive approach to quality assurance. This role is a full-time, permanent position and offers Hybrid working.
Benefits for you as the Quality Assurance Auditor:
30 Days Annual leave
Excellent Travel package
Pension Scheme
Progression Opportunities
Healthcare scheme
Retention bonus
Additional benefits
Your responsibilities as the Quality Assurance Auditor:
Undertake audits and report findings
Improve practice though the delivery of the Quality Assurance
Prepare reports and deliver presentations on findings
Responsible for collating, maintaining and reporting on data
Requirements of you as the Quality Assurance Auditor:
A recognised Social Work qualification (Degree/DipSW/CQSW)
A valid registration with Social Work England
Understanding and Knowledge of compliance with health and safety
Must hold a full UK Driving Licence
Location: North London
Salary: Up to £59,400 per annum
Please follow the instructions on this website, or alternatively contact Tom McKenna on 07587 031100 or tmckenna@charecruitment.com for further details and please do be sure to leave your contact details
If this position isn't what you are looking for, but you are looking to make a move within Social Work, get in touch, as we have many other opportunities!
https://www.charecruitment.com
https://www.linkedin.com/in/permanentsocialworkrecruitment/....Read more...
Regulatory Affairs and Quality Assurance Assistant – Medical Devices - Cambridge
Due to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the company’s Quality Assurance and Regulatory Affairs Manager. The team provide quality assurance and regulatory affairs advise on the creation of new products and the improvement of existing technologies.
It would be highly advantageous if you have knowledge of design processes, but it’s not essential. This team does not just fill out quality assurance and regulatory documents; this is a team where they will be very involved with the R&D team, providing vital advice on the creation of medical devices, and ensuring the team operates within the FDA 510k, ISO 13485, and FDA 21 CFR Part 820 standards.
It would be ideal if you have both quality assurance and regulatory affairs knowledge. However, people have moved into this role from either regulatory affairs or quality assurance background, but with a general knowledge in the other side.
It is essential that you have medical devices knowledge, especially ISO 13485 and FDA 510k knowledge. Although writing submissions will not be a major part of your role, you will relay information to the teams responsible for this, so ideally you will have done this in the past or at least assisted.
Ideally, you will have QMS experience. If you do have this knowledge, I would advise making it clear on your CV as this is highly desirable in this role.
The products this company has been developing are industry-changing and will improve the lives of people around the world.
It is expected that you would hold a 1st or 2:1 degree within an engineering or sciences discipline along with some experience within regulatory affairs or quality assurance. Although experience working within a medical devices R&D or design team is more important than education.
This is a growing company; due to this, they offer career progression, excellent salary, benefits package, the chance to work on life-improving devices, and share options.
If you have regulatory affairs knowledge in the medical devices sector and are looking for a challenging role, then apply now.
I expect a lot of interest in this role, and the company are looking to recruit quickly. So, if you are interested in this role, I suggest applying immediately or risk missing out.
For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment, Science recruitment and Biotech recruitment specialists Newton Colmore Consulting, on +44 121 268 2240 or make an application, and one of our team at Newton Colmore Consulting will contact you.....Read more...
Quality Assurance Engineer with proven experience in the Aerospace / Manufacturing sector, strong understanding of Quality Management Systems (QMS) and excellent knowledge ISO 9001 & AS 9100 (desirable) is required for a permanent position for a global company in the Oldham / Ashton-under-Lyne area. Competitive salary (DoE) plus excellent benefits, working 38 hours/week, Mon – Fri days (8:00am – 4:20pm). This is a fantastic opportunity, with security and long term career prospects.
Package:
Competitive Salary (dependent on experience and qualifications).
38 hour week typically 8:00am – 4.20pm (core hours)
25 days holiday + bank hols
Company pension scheme
Profit related bonus
Job Objective: Under the guidance of the QHSE Manager, the QA Engineer will assume a pivotal role in maintaining the quality and efficiency of company processes, products, and systems. The responsibilities will include, driving process enhancements, Problem solving and safeguarding the integrity of the management systems through leadership and analysis of data.
The successful Quality Assurance Engineer day to day duties will include:
Analyse data to identify opportunities for improvements and efficiencies, providing analytical reports for management. Highlight key findings and propose recommendations that are proportionate to the risk.
Oversee and lead the customer complaints process, ensuring timely resolution within the business & team, and ensure effective communication with relevant departments.
Conduct regular internal audits as per the plan to assess compliance with quality standards EN9100 and identify areas for improvement.
Collaborate with manufacturing engineers on customer requirements to ensure compliance within the Production environment.
Assist in general Upkeep & continual improvement of the QMS to ensure compliance to EN9100.
Develop inspection and risk management methods to analyse product quality in line with customer requirements such as MSA, FMEA, CPK.
Perform specification reviews to ensure our products align with the specified requirements.
Develop and provide training to staff on internal quality processes, standards, and best practices.
Ensure the protection of Company Intellectual Property and Customer Confidentiality.
Perform any other tasks and duties as required by management.
The ideal Quality Assurance Engineer / Quality Co-ordinator will have the following experience, skills and characteristics:
Proven experience in a quality engineering role (preferably in an Aerospace environment)
Strong understanding of quality management systems and ISO 9001 / AS9100 standards.
Experience in conducting internal and external quality audits to verify compliance with standards and regulations.
Proficient in creating and maintaining accurate quality documentation, reports, and records to facilitate traceability and continuous improvement.
Excellent analytical and problem-solving skills.
Effective communication and collaboration abilities.
In-depth knowledge of Microsoft Office applications.
Ideally experience in ERP systems such as Navision or similar.
Knowledge of Quality toolbox including FMEA, Root cause investigations, Lean and Six Sigma tools & techniques.
Confident in the use of IT software (MS Office, QMS, Reports etc.) and strong administration skills.
Ability to carry out data collection and analysis resulting in identification of improvement opportunities.
Establish good level of cooperation with colleagues with colleagues and parent company.
Key Words: Quality Assurance Engineer, Quality Engineer, Quality Co-ordinator, Quality Technician, Quality Assurance, Quality Inspection, QA, QC, QMS, Quality Management System, ISO9100, AS9100, ERP, Navison, Data Analysis, Manufacturing, Production, Advanced Composite Materials, Aerospace, Automotive, Lean Manufacturing, Oldham, Ashton-under-Lyne, Manchester, Bolton, Bury, Rochdale
The successful Quality Assurance Engineer will need to be flexible as there will be a requirement to work additional hours as and when the business requires and other duties not mentioned in this job description. You will also have the relevant qualifications and experience, be self-motivated, able to work under pressure, organised, analytical, logical, excellent communicator, work alone and also as part of a team.
If you are interested Quality Assurance Engineer and have the required experience please click on the apply now button....Read more...
We have an exciting opportunity for a Quality Assurance Auditor to join a fast-growing CRO based in the Cheshire area. As the Quality Assurance Auditor you will be required to give advice on the compliance and quality issues, and look for improvement opportunities to working practices to ensure the company's GLP and GCP regulations are maintained.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Assurance Auditor will be varied however the key duties and responsibilities are as follows:
1. You will be mainly part of the busy QA team to assure management that the facility is operating in compliance with the UK GLP regulations. This involves scheduling work within the QA team and co-ordinate activities for the QA unit.
2. You will be required to review study plans to ensure the GLP regulations are followed, as well as audit scientific reports, to ensure that the reports fully and completely describe the data generated on studies.
3. You will be responsible the inspection of the study procedures, laboratory processes and facilities, interacting with staff at all levels. You will also advise upon and audit computerised system validation activities and assure validation documentation is in compliance with regulatory requirements.
4. Additionally, as the QA Auditor, you would design and deliver GLP and GLP training to the scientific team and support the test facility manager in the planning and hosting of external client audits and government agencies.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Quality Assurance Auditor we are looking to identify the following on your profile and past history:
1. Relevant degree in Life Sciences or a chemistry related subject (e.g. Biochemistry)
2. Proven industry experience working in a GLP testing facility is essential as well as experience of working in a quality role under GLP or GCP.
3. You will need to have an eye for detail and the determination to complete tasks to a high standard within tight deadlines.
Key Words: Quality Assurance Officer | QA Officer | GLP | GCP | Documentation | Quality and Compliance | Testing | CAPA | Root Cause Analysis
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.....Read more...
Quality Engineer – Cambridge – Medical Devices
We are currently looking for a Quality Engineer for a growing Medical Devices organisation based in Cambridge. The company work on a range of different Medical Devices, providing a variety of projects and tasks in your role.
You will collaborate various Medical Devices experts, including Mechanical Engineers, Physicists, Electronics Engineers, Software Engineers, and other professionals. Your primary focus will be on Quality Assurance of Medical Devices to ISO 13485 standards, although knowledge of EN 60601 would also be advantageous.
Your responsibilities will include creating technical files and testing documentation. If you have experience of Design Assurance, this would also enhance your approach to this work.
We would expect you to have a degree that led you into a Medical Devices Quality Engineering career. However. if you have another route into a Medical Devices role, we would still be keen to hear from you.
In addition to working on various Medical Devices, you will be rewarded with an excellent starting salary, a bonus, a generous pension, life assurance, healthcare, and other excellent benefits.
Given the anticipated interest in this role, if you are looking for a new opportunity, I suggest making an application now to avoid missing out.
For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment, Science recruitment and Biotech recruitment specialists Newton Colmore Consulting, on +44 121 268 2240 or make an application and one of our team at Newton Colmore Consulting will contact you.....Read more...
£42,000 - £45,000 + Bonus + BenefitsIn order to uphold our client’s exceptionally high standards of product excellence, a passionate and proactive Quality Assurance Manager is required to join one of the UK’s leading suppliers of niche consumable products to the heating and plumbing industry.
The successful candidate will become a crucial member of the team working company-wide to ensure conformance of all aspects of the day-to-day business. This will include everything from auditing our own processes and procedures, sorting, testing and recording of product returns, arranging independent audits of our supply chain, and working with calibration equipment, test labs and certification agencies.
The ideal QA Manager will have previous experience of implementing ISO 9001 and 14001 Management Systems, with the ability to ensure the business and its processes adhere to the strictest standards. Key Responsibilities
Deliver a company-wide quality assurance programme, including implementation of ISO9001 and ISO14001
Act as the go-to expert for all things quality and conformance related
Setting up a new lab within the Head Office, for R&D and the calibration of pressure meters, ensuring their accuracy and reliability
Log all instances of product related non-conformance
Analyse causes, identify solutions and recommend actions to be taken to resolve quality
Drive the corrective & preventative action (CAPA) process for the business.
Assist in the resolution of technical and quality issues
Perform internal audits in support of the internal audit programme
Fully investigate & respond to customer complaints
Maintain and improve Internal Quality Assurance System
Handle queries from end-users and internal departments, ensuring total satisfaction
Skills & Experience
Proven experience in QA management, with hands-on experience of ISO 9001 / 14001 Management Systems and accreditations
Knowledge of electrical safety standards and compliance
Expertise in “Goods In” processes and procedures and handling of non-conformances
Strong leadership and coordination skills, with the ability to effectively manage and motivate teams and work on own initiative
Exceptional problem-solving abilities and a customer-centric mindset
Advanced MS Excel skills for analysis and reporting
This is a fantastic opportunity for an ambitious Quality Assurance professional to become part of a team dedicated to excellence! If you're ready to take on this exciting challenge and make a real impact, we want to hear from you. In return for your commitment, a competitive salary and employee focussed benefits package is on offer. Apply now!....Read more...
There a new exciting opening with our client who is a globally recognised research and development company, focused on advancing solutions to improve the design and safety of products across multiple industries.
They are currently looking for a Salesforce QA Engineer to join their team, remotely in Germany but with some site visits to their team based in Breman, possible 5-6 times a year. This person will provide quality assurance support on all salesforce implementations.
Skills & Requirements:
Ability to own the QA process from design through to troubleshooting and testing setup
Ability to conduct unit, functional, smoke and integration testing
Experience in writing clear and detailed test plans and cases
Experience:
3- 5 years experience in quality assurance relating to Salesforce sales, services and cloud product knowledge, possibly Salesforce CPQ as well would be an advantage
Bachelor degree or equivalent and professional experience in Salesforce Quality assurance
Basic knowledge of SOQL, SOSL, JavaScript, HTML, JSOM and REST API
Fluency in English language
If interested, please get in touch for a confidential discussion with our consultant using the contact details provided or click “Apply” to send an up-to-date copy of your CV and ideally a covering letter.
Cavendish (Recruitment) Professionals Ltd are proud to be an equal opportunity employer and we believe that inclusivity begins with the candidate experience. All qualified applicants will receive consideration for employment regardless of, gender, race, age, sexual orientation, religion, or belief.....Read more...
Are you a Quality Engineer - Electronics looking for an exciting job opportunity in Cambridge?
My client is a leading designer and manufacturer of high-performance Electronic Controllers for Lighting and recognition systems. For this Quality Assurance Manager – Manufacturing, they are looking for someone to own the QMS for the company standards to ISO 9001 and deliver quality products to the highest standards across all company functions.
Main responsibilities for this Quality Engineer - Electronics are:
- Responsibility for the maintenance of QMS. Keeping up to date with all regulatory requirements and compliance standards adopted by the company
- Formulation, continual development & promotion of policies, processes and procedures, objectives, and measures as required for the continued operation of QMS – e.G. Quality & Environment.
- Responsible for managing both internal and external audits
- Collation and delivery of performance data as part of QMS review to senior management
- Working with Engineering departments to carry out the reliability testing of products under development.
Key skills and experience required for this Quality Engineer - Electronics:
- Proven experience in quality assurance, preferably in development and manufacturing of electronics production environment.
- Working knowledge of quality improvement, problem solving and analysis techniques, for example: TQM, 5Why, 8D, R&R Studies, FMEA’s for process and product, Ishikawa diagrams, SPC, etc.
- Have good interpersonal skills for cohesive relationships with all areas of the company and external bodies.
- Experience working to ISO9001 standards
To apply to this excellent Quality Engineer - Electronics, opportunity based in Cambridge, please email a copy of your CV to Sophie Khuttan – SKhuttan@redlinegroup.Com quoting reference SKK1092, or for more information, please call Sophie on 01582 878817 / 07961158586. ....Read more...
Merton Council are recruiting for a Adult Social Care Quality Assurance Auditor
Knowledge
Advanced knowledge of learning and development for adult social care.
Advanced knowledge of adult’s social care, with regards to policy, legislation, regulation and the implications for social care and Occupational Therapist.
Advanced up to date knowledge of CQC Local Authority Assessment framework.
Advanced knowledge of London Pan London policy as well as safeguarding legislation and procedure.
Advanced knowledge and understanding of performance management and quality assurance frameworks, reporting and practice.
Skills
Ability to work with datasets to draw out insight and intelligence to inform policy and service improvement.
Ability to work alone and prioritise own workload. The ability to work to deadlines.
Ability to write succinct, accurate, professional reports arising from Quality Assurance visits and other activity.
Broad knowledge of public policy and the current and emerging local government policy, political and financial landscape
Willingness to be innovative and apply innovative approaches, such as restorative practice and a strengths-based approach, to develop the Council’s thinking about service development and transformation
Experience/Training
A registered social worker, with substantial post-qualifying experience e.g. Practice Educator or Practice Teacher. Experience of learning and development professional experience of working in the Adult social care sector
Experience of contributing to workforce strategies and training plans.
Experience working with partner agencies in the private sector and other external agencies - both statutory and voluntary
Experience of undertaking training needs analysis and commissioning training
Experience of using and developing a quality assurance and performance framework that measure and evidence outcomes
Experience of developing and implementing workforce strategies
Experience of office systems, e.g. word, excel
Demonstrable experience of dealing with complex issues, particularly involving customers.
please call 01772 208964 or email Delanie at Delanie.heyes@servicecare.org.uk....Read more...
Quality Assurance EngineerWythenshaweContractQuality Assurance EngineerThe RoleThis is a role leading establishing processes, setting efficient controls into processes to ensure achieving planned results and outputs including process capacity, capability, costs, and quality. This role has close working relationship with quality team members, with NPD, engineering, process, production, tooling, operations, internal and external customers and suppliers. Quality Assurance EngineerMain Responsibilities
Engage with internal and external customers, engineering, tooling, production, operations, and other relevant stakeholders to address internal and external non-commences, concerns and complaints.Lead problem resolution for system, process, and product issues and subsequent implementation of containment actions. Able to determine root cause analysis and ensure effective implementation of corrective and/or preventative actions. Preparation of 8D reports.Perform internal audits in line with annual audit plan, delivering robust internal processes that are fit for purpose and drive high standards.Assist with the implementation, maintenance, monitoring and evaluation requirements within the business system including supplier quality management.Train teams and individuals effectively on quality procedures, ensuring compliance to best practices across the business functions.Provide instructions for successful implementation of process changes, including system, supplier, customer, engineering, and internal business changes. Monitor changes and their results.Support & develop other quality team members with their roles and responsibilities.Lead weekly meetings with process related functions in organization (production, NPD, engineering, processing, etc.), acting as first point of contact for queries.Support process improvement & problem-solving meetings.Support other quality functions within HT Manchester team during all relevant activities.
Quality Assurance EngineerThe Candidate
Knowledge of injection moulding process and tooling manufacturing process.Experience of working in a manufacturing environment and in a safe and effective mannerPrevious quality assurance experience and demonstrated use of quality tools/methodology, including problem-solving methodologies.Experienced in writing process documentation including Works Instructions, Quality Control Plans, and relevant quality documentation.General experience in a variety of manufacturing processes and ability to work within a team and as an individual contributing in a fast-paced, changing environment.Knowledge and understanding of SPC, DOE, Six Sigma, lean methodology and associated tools and techniques.Knowledge and understanding of automotive core tools.Knowledge and understanding of quality standards: AS 9100, ISO 9001, IATF 16949.Internal auditor qualification and experience.Ability to multitask, prioritise and meet deadlines in timely manner.Excellent attention to detail with a creative attitude and proactive naturePC skills & experience in the use of MS OfficeGood communication skills in English language, written & oralWilling to invest in continuous professional development of self
Please contact Adam Lang at Winsearch UK for further information.Adam Lang - adam.lang@winsearch.ukWinsearch acts as an employment agency for permanent staff. We recruit for roles based in Engineering & Manufacturing, Food & Drinks, Pharmaceutical, Supply Chain & Procurement and Professional Services. View our latest jobs today on our website http://www.winsearch.uk and follow us on LinkedIn. Our clients and their customers come from diverse backgrounds and so do we. We hire our people from various walks of life, each of whom make our company stronger with their talent, uniqueness, and expertise. This is what makes our company special; if you want to help us grow and take this ethos to our clients, then we cannot wait to collaborate with you!
The UK has now left the European Union. Any EU, EEA or Swiss citizens living in the UK that wish to remain in the UK post Brexit need to apply to the EU Settlement Scheme. Although the closing date for applications was 30th Jun 2021, if you have not yet applied but believe that you would qualify under the EU Settlement Scheme, the Home Office have confirmed that they will consider late applications. For further information please see https://www.gov.uk/browse/visas-immigration/eu-eea-swiss
Many Thanks....Read more...
Maxxima have recently partnered with one of the UKs specialist provider of diagnostic and healthcare solutions. We are currently looking for an experienced Pharmacist, who can provide overall support for the clinical leadership of the service. This post is based in Derbyshire, which is easily accessible via public transport.
About the role:
As a Pharmacist, you will provide expert leadership in quality assurance across various departments and services. This includes overseeing the Quality Assurance Department, Pharmacy Aseptic services, Pharmacy wholesale dealing, Nuclear Medicine Services, and external customer services.
Your main responsibilities as a Pharmacist:
- Act as the quality controller to meet MHRA/Section 10 licensing requirements for various units and services.
- Plan and deliver QA services to the Royal Derby site and external customers.
- Plan fridge temperature monitoring for different sites.
- Act as RDH Quality Controller for batch releases.
- Lead external inspections and audits.
- Ensure compliance with GMP standards and approve SOPs for QA & Aseptic Services.
- Manage quality management systems related to MHRA licensed services.
- Develop commercial opportunities and partnerships.
- Coordinate with production managers for testing and inspection schedules.
- Provide expert advice on GMP and ensure individual and team performance through recruitment, training, and management.
- Engage in strategic service planning, capacity management, and securing funding for service developments.
What we are looking for in a Community Pharmacist:
- GPHC registered
- Science degree or equivalent, with post-qualification specialist knowledge.
- Significant post-registration hospital or pharmaceutical practice experience.
- Accredited 'Quality Controller' by MHRA.
- Specialist knowledge and experience of GMP, GCP, and GDP.
Why work with Maxxima?
- Knowledgeable, dedicated and vastly experienced Permanent Team with longstanding professional relationships with multiple clients
- Access to exclusive vacancies through our numerous Master Vendor trusts across the country
- Vacancies outside of NHS Rate caps with our private sector agreements
- Access to International roles outside of England and the United Kingdom
Please note: We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List.
Next steps:
If you are interested to hear more, either hit the APPLY NOW button or reach out to Paola on 02033986694 or Paola.Humeres@maxximagroup.com....Read more...
Maxxima have recently partnered with one of the UKs specialist provider of diagnostic and healthcare solutions. We are currently looking for an experienced Pharmacist, who can provide overall support for the clinical leadership of the service. This post is based in Derbyshire, which is easily accessible via public transport.
About the role:
As a Pharmacist, you will provide expert leadership in quality assurance across various departments and services. This includes overseeing the Quality Assurance Department, Pharmacy Aseptic services, Pharmacy wholesale dealing, Nuclear Medicine Services, and external customer services.
Your main responsibilities as a Pharmacist:
- Act as the quality controller to meet MHRA/Section 10 licensing requirements for various units and services.
- Plan and deliver QA services to the Royal Derby site and external customers.
- Plan fridge temperature monitoring for different sites.
- Act as RDH Quality Controller for batch releases.
- Lead external inspections and audits.
- Ensure compliance with GMP standards and approve SOPs for QA & Aseptic Services.
- Manage quality management systems related to MHRA licensed services.
- Develop commercial opportunities and partnerships.
- Coordinate with production managers for testing and inspection schedules.
- Provide expert advice on GMP and ensure individual and team performance through recruitment, training, and management.
- Engage in strategic service planning, capacity management, and securing funding for service developments.
What we are looking for in a Community Pharmacist:
- GPHC registered
- Science degree or equivalent, with post-qualification specialist knowledge.
- Significant post-registration hospital or pharmaceutical practice experience.
- Accredited 'Quality Controller' by MHRA.
- Specialist knowledge and experience of GMP, GCP, and GDP.
Why work with Maxxima?
- Knowledgeable, dedicated and vastly experienced Permanent Team with longstanding professional relationships with multiple clients
- Access to exclusive vacancies through our numerous Master Vendor trusts across the country
- Vacancies outside of NHS Rate caps with our private sector agreements
- Access to International roles outside of England and the United Kingdom
Please note: We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List.
Next steps:
If you are interested to hear more, either hit the APPLY NOW button or reach out to Paola on 02033986694 or Paola.Humeres@maxximagroup.com....Read more...
Quality Inspector
Quality Inspector Salary: £28-38k (dependent on experience)
The Company
Specialising in a fast-growing industry, housed in a huge, purpose-built facility, this company is seeking a skilled Quality Inspector to join their team permanently. It is a leading UK manufacturer with plenty of long-term relationships that have resulted in plenty of repeat business, unfazed by competition and forging full steam ahead.
Quality Inspector Role & Responsibilities
- Quality Assurance: Perform final inspections of completed products, conduct internal audits, investigate quality issues, and ensure compliance with industry-specific and fire safety standards.
- Process Improvement: Monitor and continuously improve manufacturing processes, manage document control, and calibrate measuring equipment.
- Product Compliance: Verify that manufactured products meet specifications and standards throughout production and storage.
- Cross-departmental Support: Collaborate with other teams within the business on supplier quality checks and provide quality advice where possible.
- Training & Paperwork: Happy to complete audits, and other necessary paperwork and train other staff if needed
- Other Bits: Familiar with ISO 9001 and/or ISO14001, able to work from technical drawings and possess a full UK driving license
What Next?
Apply now or call/message Hayden at Holt Engineering for more information on the Quality Inspector role on 07955 081 482.....Read more...
Join our team as a Parts Quality Assurance Engineer, where you'll play a crucial role in ensuring the delivery of high-quality services to our clients. We're seeking a dynamic individual with technical expertise, strong communication skills, and a proactive attitude.
Responsibilities:
Support the day-to-day operation of the Quality Management System, ensuring alignment with customer requirements.
Investigate and address root causes of part-based quality issues, collaborating with cross-functional teams.
Maintain and develop local procedures and forms within the document management system.
Coordinate external supplier audits and implement improvement projects across the management system.
Liaise with global customer plants, addressing concern management issues and documentation submissions
Requirements:
Proficiency in ISO9001 and IATF16949.
Experience in a fast-paced manufacturing environment, preferably automotive.
Knowledge of APQP, PPAP, FMEA, SPC and MSA desirable.
Awareness of Alliance New Product Quality Procedure (ANPQP).
Willingness to travel as needed.
Experience:
Automotive industry experience preferred.
Familiarity with Quality Tools such as 5WHY, Ishikawa, etc.
Proficient in MS Office tools (Word, PowerPoint, Excel, Access & SharePoint).
Background in disciplines such as Body in White, Vehicle Trim, Electrical Architecture, or EV Powertrains is a plus.....Read more...
Quality Engineer
Motorsport
Engineering Manufacturing Industry
Peterborough PE3
Up to £45k per annum, depending on experience
33 Days Holiday and Pension
Are you an experienced Quality Engineer with experience implementing processes and looking to join an established family run engineering business? Are you passionate about the Motorsport industry? If so read on..
Our established client specialises in Engineering Manufacturing for the Motorsport industry. They are currently looking for a new Quality Engineer to join their established team. Commutable from Peterborough, Stamford, Ramsey and Corby.
Duties Include - Quality Engineer:
- Develop and implement quality assurance policies, procedures and processes
- Developing industry standard reporting; 8D, 5Y, PPAP, APQP, PFMEA processes to better tackle quality issues
- Root cause analysis
- Hands-on inspection
- Dealing with customers face-to-face
- Working to specifications
Key Skills / Experience Required - Quality Engineer:
- Must have worked as a Quality Engineer within the engineering manufacturing industry
- Motorsport or Automotive background is ideal
- Quality checking experience on metal components or products
- Degree qualified in suitable subject
- Great understanding of quality improvement procedures
- ISO 9001:2015 experience
- Able to commute to the Peterborough area
- Self-motivated, enthusiastic and a high standard of personal performance
- Flexible, reliable and a strong team player
The Package - Quality Engineer
- Starting salary of up to £45k per annum, depending on skill level and experience
- 33 days holiday
- Pension
- Death in service
Interested? To apply for this Quality Engineer position, here are your two options:
1. "This is the job for me! When can I start?" - Call 0116 2545411 now and lets talk through your experience. Ask for Nilam between 8.30am - 5.30pm.
2. "I think I'm right for this position, but I'm not sure I have enough to get an interview" - Click "apply now" so I can read your CV and let you know
PPDEL....Read more...
QA - Quality Auditor - Nights Bristol - Central Food Manufacturing £28,080 This is a fabulous opportunity to join an established and developing Food Manufacturer of premium products in a QA / QC / Quality Auditor role.HoursPermanent Night Shift available 9pm - 05.30 shift Monday to Friday The QA - Quality Auditor role will involve:
Ensure food safety, legality, quality and authenticity procedures are continuously implemented.Demonstrate & promote a positive food safety culture, including good manufacturing practise and working in clean, safe manner.Check products meet quality specifications and compliance standards.Production records and checks including labelling, intake, production.Sample collection, admin and analysis/trend results.Traceability and mass balance checksAssist during third party audits.
QA - Quality Auditor Experience Required:
Experience of operating in a QA / QC roleStrong written and verbal communication skillsStrong attention to detail and ability to spot defects or inconsistencies.Knowledge of quality assurance principles, methodologies, and toolsAbility to work independently and as part of a team.Good communication skills, both verbal and written
If the role is of interest, then please contact us today....Read more...
Holt Executive are currently partnered with a leading Global Satellite and Space leader that provides reliable and secure satellite-delivered voice and high-speed data communications solutions to broadcast, telecommunications, corporate and government customers worldwide. Their Low Earth Orbit (LEO) satellite network is revolutionizing global broadband connectivity.
Our partner is seeking a Senior Manager, Software User Terminals to spearhead the development and implementation of strategies for the software development environment, as well as to manage a team of software professionals.
This Senior Manager, Software User Terminals opportunity offers a hybrid work environment and requires international travel.
Key Responsibilities for the Senior Manager, Software User Terminals:
- Develop and present SW development status reports, highlighting accomplishments, challenges, and risks.
- Strategise and implement risk mitigation strategies to ensure successful software development outcomes.
- Create an inclusive and positive working environment where every team member can thrive.
- Lead a geographically dispersed team, promoting effective communication, collaboration, and alignment across locations.
- Drive software automation initiatives and champion quality assurance practices to enhance software development processes and product reliability.
- Organise team-building events, workshops, and knowledge-sharing sessions to foster team cohesion and professional growth.
Key Skills & Experience Required by the Senior Manager, Software User Terminals:
- Bachelor's or Masters degree in Computer Science, Computer Engineering and Electrical Engineering, or a related field.
- Minimum of 10 years of management experience in a software development environment, preferably with embedded software focus.
- Strong background in embedded software development and proficiency in Agile methodologies.
- Proven leadership skills with a track record of building and managing successful software development teams.
- Technical expertise in software engineering practices, including design, development, and testing.
- Experience working with geographically dispersed teams.
- Familiarity with automation practices and quality assurance methods.
- Proficiency in working with both public and private cloud environments.
- Familiarity with CloudOps and FinOps practices.
- Familiarity with setting up and managing CI/CD pipelines.
If your skills and experience match this Senior Manager, Software User Terminals opportunity, we encourage you to apply by sending your CV to info@holtexecutive.com....Read more...
QUALITY ASSURANCE OFFICER DUDLEY - HYBRID WORKING £35,000
THE OPPORTUNITY
I’m pleased to be working for a well-established Insurance Company who have experienced some impressive growth over the past few years and who, as a result, are needing to expand their compliance team. They are looking for an experienced Compliance professional from the insurance space to focus on undertaking Quality assurance audits. It is part of their ethos to provide flexibility in their workplace which is why they provide the opportunity to work from home 3 days a week to promote employee satisfaction and well being.WHATS IN IT FOR YOU?
Up to £35,000 based on experience.
Hybrid working- 2 days a week in the Dudley office.
26 days holiday + bank holidays.
Fully planned, immersive training plan.
Death in service.
Health Cash Plan.
Free parking.
Support in achieving your Insurance qualifications (ie, the CII)
KEY RESPONSIBILITIES
Undertaking technical underwriting audits to ensure the underwriters are adhering to FCA legislations.
Offering feedback to underwriters both positive and constructive on their performance.
Dealing with high volume referral audits
Conducting a small number of call assessments.
Working in conjunction with the Risk and compliance manager to manage workload.
PERSON SPECIFICATION
Strong Background within Compliance and the Insurance Industry
CII qualifications a major bonus
Clear and up to date knowledge of current FCA regulations
Positive attitude and desire to get stuck in.
TO APPLY We are currently shortlisting for interview so submit your CV for immediate consideration.
Get Recruited is acting as an Employment Agency in relation to this vacancy.....Read more...
Business Operations Coordinator
Location: Darlington, Durham (Hybrid)
Salary: £25k - £35k + Excellent Benefits
Working Hours: 35 hours per week
The Client:
Our client is a renowned supplier of computerised systems for managing dangerous goods in sea transport, supporting global entities in shipping, distribution, warehouses, ports, and regulatory bodies.
The Role:
As a Business Operations Coordinator, youll assist the Operations Manager and Chief Information Officer, collaborating across departments and contributing to projects that add value to the organisation.
Duties:
? Assist in monitoring customer contracts and maintaining CRM accuracy.
? Support Operations Manager in internal audits for process enhancement.
? Respond to Service Desk queries regarding licenses and e-learning.
? Enhance internal information flow and process workflows.
? Collaborate for improved project efficiencies.
? Perform general business administration tasks as needed.
Requirements:
Essential:
? Previously worked as a Business Operations Coordinator or in a similar role.
? CRM and Service Desk application experience.
? Understanding of quality assurance audit processes.
? Collaboration skills with cross-functional teams.
? Prioritisation skills and Microsoft Office proficiency.
Good to have:
? Skilled in utilising Project Management software.
? Exposure to business-to-business environments.
? Familiarity or comprehension of ISO standards.
Benefits:
? Hybrid working options.
? Simply Health Cash Back scheme
? Life Assurance (Death in service)
? Company pension
? Discretionary Bonus
? 25 days holidays plus bank holidays
Apply now for an opportunity to contribute to exciting projects and advance your career in a global maritime organisation.
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Additional Resources will be acting in ....Read more...
Maxxima have recently partnered with one of the UKs specialist provider of diagnostic and healthcare solutions. We are currently looking for an experienced Lead Occupational Therapist, who can provide overall support for the clinical leadership of the service. This post is based in Cambridge, which is easily accessible via public transport.
About the role:
As a Lead Occupational Therapist, you will work independently within the overall framework of the service policies and procedures you will work within existing MDT and Clinical Governance structures to support the services in future development and ensuring quality assurance.
Whats in it for you as a Lead Occupational Therapist:
- 30 days annual leave entitlement plus bank holidays
- Life Assurance
- Pension scheme with options to increase your contributions
- Your Wellbeing Matters access to a wide range of first-class mental health support services and physical health checks
- 4 day working week with full pay *T&C's apply
And a market-leading benefit offering through our Flexible Benefits Platform, Vista, enables you to choose the package thats right for you, including:
- A wide range of health, wellbeing, and insurance benefits
- 100s of discount options valid in the UK and abroad
- Cycle to Work Schemes
- Electric Car Purchase Scheme
- Critical illness cover
Your main responsibilities as a Lead Occupational Therapist:
- Working independently within the overall framework of the service policies and procedures
- Work within existing MDT and Clinical Governance structures to support the services in future development and ensuring quality assurance
- Help maintain a strong safeguarding culture, and ensure the pupils we support are heard, respected, and involved in decisions that affect them wherever possible
What we are looking for in a Lead Occupational Therapist:
- Degree in Occupational Therapy
- Registered with the HCPC
- Experience in managing multi-disciplinary teams
- Experience of working with people who have an intellectual disability and/or autism with additional needs (e.g. complex trauma, mental health needs, behaviours of concern)
- Demonstrable ability to lead and manage strategically
- Ability to work collaboratively with a range of key partners
- Able to work sensitively with people and resolve conflict effectively
- Evidence of continuing professional development relevant to the setting
- Substantial and relevant post-qualification experience with adults
- Experience of lecturing/teaching/training
- Skills in the management of data are also important as the role includes collecting and analysing data to inform various pieces of service delivery, development and project work
Why work with Maxxima?
- Knowledgeable, dedicated and vastly experienced Permanent Team with longstanding professional relationships with multiple clients
- Access to exclusive vacancies through our numerous Master Vendor trusts across the country
- Vacancies outside of NHS Rate caps with our private sector agreements
- Access to International roles outside of England and the United Kingdom
Please note: We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List.
Next steps:
If you are interested to hear more, either hit the APPLY NOW button or reach out to Lucy on 0117 471 5956 or lucy.holmes@maxximagroup.com....Read more...
Maxxima have recently partnered with one of the UKs specialist provider of diagnostic and healthcare solutions. We are currently looking for an experienced Lead Occupational Therapist, who can provide overall support for the clinical leadership of the service. This post is based in Rutland, which is easily accessible via public transport.
About the role:
As a Lead Occupational Therapist, you will work independently within the overall framework of the service policies and procedures you will work within existing MDT and Clinical Governance structures to support the services in future development and ensuring quality assurance.
Whats in it for you as a Lead Occupational Therapist:
- 30 days annual leave entitlement plus bank holidays
- Life Assurance
- Pension scheme with options to increase your contributions
- Your Wellbeing Matters access to a wide range of first-class mental health support services and physical health checks
- 4 day working week with full pay *T&C's apply
And a market-leading benefit offering through our Flexible Benefits Platform, Vista, enables you to choose the package thats right for you, including: - A wide range of health, wellbeing, and insurance benefits
- 100s of discount options valid in the UK and abroad
- Cycle to Work Schemes
- Electric Car Purchase Scheme
- Critical illness cover
Your main responsibilities as a Lead Occupational Therapist:
- Working independently within the overall framework of the service policies and procedures
- Work within existing MDT and Clinical Governance structures to support the services in future development and ensuring quality assurance
- Help maintain a strong safeguarding culture, and ensure the pupils we support are heard, respected, and involved in decisions that affect them wherever possible
What we are looking for in a Lead Occupational Therapist:
- Degree in Occupational Therapy
- Registered with the HCPC
- Experience in managing multi-disciplinary teams
- Experience of working with people who have an intellectual disability and/or autism with additional needs (e.g. complex trauma, mental health needs, behaviours of concern)
- Demonstrable ability to lead and manage strategically
- Ability to work collaboratively with a range of key partners
- Able to work sensitively with people and resolve conflict effectively
- Evidence of continuing professional development relevant to the setting
- Substantial and relevant post-qualification experience with adults
- Experience of lecturing/teaching/training
- Skills in the management of data are also important as the role includes collecting and analysing data to inform various pieces of service delivery, development and project work
Why work with Maxxima?
- Knowledgeable, dedicated and vastly experienced Permanent Team with longstanding professional relationships with multiple clients
- Access to exclusive vacancies through our numerous Master Vendor trusts across the country
- Vacancies outside of NHS Rate caps with our private sector agreements
- Access to International roles outside of England and the United Kingdom
Please note: We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List.
Next steps:
If you are interested to hear more, either hit the APPLY NOW button or reach out to Lucy on 0117 471 5956 or lucy.holmes@maxximagroup.com....Read more...