3rd Line IT Support Engineer Oxfordshire / On-Site with occasional travel £40,000 - £45,000 + bonus, share scheme, private dental and medical, a generous pension and more Full Time / Permanent The Role and Company My client, a well-established professional services organisation, is looking for an experienced 3rd Line IT Support Engineer to join their small but growing in-house IT Team. The role will be a combination of both support (2nd and 3rd Line) and exciting project work working closely with the IT Manager and other IT Engineers. The role will be based just north of Oxford with very occasional travel to other offices in the UK. Responsibilities Configure and deploy infrastructure items including servers, networks, and all IT peripherals, for example: printers, scanners, mobiles devices, laptops and thin clients. Monitor and manage the IT systems using appropriate tools, and with the aid of the IT suppliers where appropriate, in order to maximise performance and uptime. Be an effective point of contact for internal IT, resolving issues or referring to 3rd parties as appropriate Support the Helpdesk Team - providing escalation to telephone support, and 1st - 3rd line support as this role is the primary escalation / cover point for the 1st/2nd line Helpdesk team. Identify areas where improvements can be made in the IT service. Take responsibility for assigned Projects and deliver them to time, cost and quality. Maintaining a high level of Cyber Security awareness and being proactive in securing our infrastructure and systems. Mentor and train other members of the Internal IT Team. Skills and Experience required Previous IT support experience, ideally 3rd line level but strong 2nd line experience is considered Good team player with flexible approach to working environment Experience with VMware virtualisation and ideally some Citrix knowledge Experience supporting and implementing Microsoft Windows Server and Microsoft SQL Supporting Microsoft Office 365 including: Email, Teams, OneDrive, SharePoint Good working knowledge of Multi-Factor Authentication Good working knowledge of networking: Firewalls, Switches, Patching and Wi-Fi Experience of supporting backup tools such as Veeam Supporting Domain Services including Active Directory and Group Policy Ability to deliver major system upgrades, complete change control and project work Good documentation skills with an eye for details and accuracy: technical change controls, user guides, business processes, standards, policies and procedures Please apply via the link or contact for more information. Modis International Ltd acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers in the UK. Modis Europe Ltd provide a variety of international solutions that connect clients to the best talent in the world. For all positions based in Switzerland, Modis Europe Ltd works with its licensed Swiss partner Accurity GmbH to ensure that candidate applications are handled in accordance with Swiss law. Both Modis International Ltd and Modis Europe Ltd are Equal Opportunities Employers. By applying for this role your details will be submitted to Modis International Ltd and/ or Modis Europe Ltd. Our Candidate Privacy Information Statement which explains how we will use your information is available on the Modis website.
Apr 23, 2024
Full time
3rd Line IT Support Engineer Oxfordshire / On-Site with occasional travel £40,000 - £45,000 + bonus, share scheme, private dental and medical, a generous pension and more Full Time / Permanent The Role and Company My client, a well-established professional services organisation, is looking for an experienced 3rd Line IT Support Engineer to join their small but growing in-house IT Team. The role will be a combination of both support (2nd and 3rd Line) and exciting project work working closely with the IT Manager and other IT Engineers. The role will be based just north of Oxford with very occasional travel to other offices in the UK. Responsibilities Configure and deploy infrastructure items including servers, networks, and all IT peripherals, for example: printers, scanners, mobiles devices, laptops and thin clients. Monitor and manage the IT systems using appropriate tools, and with the aid of the IT suppliers where appropriate, in order to maximise performance and uptime. Be an effective point of contact for internal IT, resolving issues or referring to 3rd parties as appropriate Support the Helpdesk Team - providing escalation to telephone support, and 1st - 3rd line support as this role is the primary escalation / cover point for the 1st/2nd line Helpdesk team. Identify areas where improvements can be made in the IT service. Take responsibility for assigned Projects and deliver them to time, cost and quality. Maintaining a high level of Cyber Security awareness and being proactive in securing our infrastructure and systems. Mentor and train other members of the Internal IT Team. Skills and Experience required Previous IT support experience, ideally 3rd line level but strong 2nd line experience is considered Good team player with flexible approach to working environment Experience with VMware virtualisation and ideally some Citrix knowledge Experience supporting and implementing Microsoft Windows Server and Microsoft SQL Supporting Microsoft Office 365 including: Email, Teams, OneDrive, SharePoint Good working knowledge of Multi-Factor Authentication Good working knowledge of networking: Firewalls, Switches, Patching and Wi-Fi Experience of supporting backup tools such as Veeam Supporting Domain Services including Active Directory and Group Policy Ability to deliver major system upgrades, complete change control and project work Good documentation skills with an eye for details and accuracy: technical change controls, user guides, business processes, standards, policies and procedures Please apply via the link or contact for more information. Modis International Ltd acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers in the UK. Modis Europe Ltd provide a variety of international solutions that connect clients to the best talent in the world. For all positions based in Switzerland, Modis Europe Ltd works with its licensed Swiss partner Accurity GmbH to ensure that candidate applications are handled in accordance with Swiss law. Both Modis International Ltd and Modis Europe Ltd are Equal Opportunities Employers. By applying for this role your details will be submitted to Modis International Ltd and/ or Modis Europe Ltd. Our Candidate Privacy Information Statement which explains how we will use your information is available on the Modis website.
Experienced Quality Engineer with a back ground in medical devices, who enjoys working across the full product lifecycle - from product concept through to manufacturing support. Support and maintenance of existing products, strong technical knowledge of quality systems, proficiency in change controls, continuous improvement, risk management, and verification/validation activities. Experience of Electro/Mechanical Assemblies or a similar technical background. Client Details PageGroup Scotland are delighted to be supporting Emblation - an award-winning medical technology company, revolutionising the way microwave energy is used in healthcare. Their aim is to improve on traditional treatments, using the unique advantages microwaves deliver - accurate, repeatable procedures, and better clinical outcomes. Their technology is revolutionising the treatment of HPV infections globally, and is widely used in Dermatology, Podiatry and Oncology, with a number of disruptive applications under development in the fields of Cardiology and Gynaecology. The company was started in 2007 by joint co-founders and inventors behind the technology. They form part of the highly experienced management team with over 50 years of experience in this field. Emblation's medical products can be found globally and through the recently investment into the business, the company is focused on 3 primary goals: Expansion into new treatment areas Development of new markets and a wider global presence The addition of new talent to our Scottish Headquarters to bring the skills and experience needed to support our plans for growth Description Assist in the investigation, analysis and documentation of complaints, non-conforming product and CAPA including monitoring to closure. Support Supplier approvals and re-assessments in accordance with planned requirements. Assist in the development of medical systems in accordance with the Company's standard operating procedures, regulations and quality standards that apply. Assist in the management of outsourced projects including all suppliers, subcontractors, quality, and manufacturing/printing. Create, maintain and evaluate product/process trends, designing and participating in process and product changes to improve product quality. Assist in risk assessment activities for relevant processes/products (i.e. dFMEA, pFMEA) ensuring compliance with ISO14971. Assist in the validation planning and preparation of processes/products which require validation. Support QMS training activities. Profile Strong written and verbal communication skills. Strong root cause/corrective action skills. Strong analytical, problem solving skills. Experience of working to quality & regulatory standards including ISO13485. Comfortable with dealing with contractors, clients & the regulatory authorities. Understanding of Design Control and Validation. Trained in risk management. Familiarity with ERP, electronic document control systems, CAPA and training software packages. Ability to develop good working relationships with colleagues at all levels of the organisation and perform both independently and as part of a team. This role will require infrequent travel to local CEM partner so a driving license is required Job Offer Salary £30K - £40K NEG/DOE, Benefits Opportunity to be part of an award winning and dynamic business with rapid expansion across the Globe. Progression and Development opportunities with excellent career opportunities. Flexible Working start and finish times
Dec 17, 2022
Full time
Experienced Quality Engineer with a back ground in medical devices, who enjoys working across the full product lifecycle - from product concept through to manufacturing support. Support and maintenance of existing products, strong technical knowledge of quality systems, proficiency in change controls, continuous improvement, risk management, and verification/validation activities. Experience of Electro/Mechanical Assemblies or a similar technical background. Client Details PageGroup Scotland are delighted to be supporting Emblation - an award-winning medical technology company, revolutionising the way microwave energy is used in healthcare. Their aim is to improve on traditional treatments, using the unique advantages microwaves deliver - accurate, repeatable procedures, and better clinical outcomes. Their technology is revolutionising the treatment of HPV infections globally, and is widely used in Dermatology, Podiatry and Oncology, with a number of disruptive applications under development in the fields of Cardiology and Gynaecology. The company was started in 2007 by joint co-founders and inventors behind the technology. They form part of the highly experienced management team with over 50 years of experience in this field. Emblation's medical products can be found globally and through the recently investment into the business, the company is focused on 3 primary goals: Expansion into new treatment areas Development of new markets and a wider global presence The addition of new talent to our Scottish Headquarters to bring the skills and experience needed to support our plans for growth Description Assist in the investigation, analysis and documentation of complaints, non-conforming product and CAPA including monitoring to closure. Support Supplier approvals and re-assessments in accordance with planned requirements. Assist in the development of medical systems in accordance with the Company's standard operating procedures, regulations and quality standards that apply. Assist in the management of outsourced projects including all suppliers, subcontractors, quality, and manufacturing/printing. Create, maintain and evaluate product/process trends, designing and participating in process and product changes to improve product quality. Assist in risk assessment activities for relevant processes/products (i.e. dFMEA, pFMEA) ensuring compliance with ISO14971. Assist in the validation planning and preparation of processes/products which require validation. Support QMS training activities. Profile Strong written and verbal communication skills. Strong root cause/corrective action skills. Strong analytical, problem solving skills. Experience of working to quality & regulatory standards including ISO13485. Comfortable with dealing with contractors, clients & the regulatory authorities. Understanding of Design Control and Validation. Trained in risk management. Familiarity with ERP, electronic document control systems, CAPA and training software packages. Ability to develop good working relationships with colleagues at all levels of the organisation and perform both independently and as part of a team. This role will require infrequent travel to local CEM partner so a driving license is required Job Offer Salary £30K - £40K NEG/DOE, Benefits Opportunity to be part of an award winning and dynamic business with rapid expansion across the Globe. Progression and Development opportunities with excellent career opportunities. Flexible Working start and finish times
Our client, an established diagnostic imaging equipment supplier in Ireland, is now making waves across the UK and are seeking a Field Service Engineer to join their team around the Stevenage/North M25 area and ensure the operational excellence of their product portfolio. The company FMC Meditech has partnered with an exclusive radiology equipment provider who are blazing new trails across the UK healthcare market with their portfolio of medical imaging devices. This is an excellent opportunity to join a tight-knit, family-run team during an exciting phase of growth and demonstrate the far-reaching potential of their solutions. The role This role will involve the ongoing servicing, installation, maintenance and modification of our client's equipment across the East Midlands, both on-site and remotely. Liaising with customers will be a core focus - you'll plan and book your own maintenance visits to carry out preventative maintenance to maintaining uptime levels and providing first-time fix solutions when issues arise. You'll play a critical role in optimising the customer experience of the product portfolio and positioning our client as the partner of choice. Other requirements include: Building a network of established contacts Delivering quality service within timescales Ensuring rapid responses to customer queries Maintaining operational excellence for the customer base Achieving high levels of customer satisfaction Providing useful feedback concerning product acceptance and service Managing your workload and diary The requirements This role is suitable for candidates with an Electronic or Electrical HNC/HND qualification, apprenticeship, or degree. Other requirements include: Background of Field Service experience Strong knowledge of digital x-ray equipment Familiar with the installation of PC hardware and its associated software Outstanding information gathering and problem-solving skills Comfortable working individually and in a team environment Excellent communication skills (both written and verbal) Able to devise concise technical reports Responds well to feedback and personal development opportunities Organised and able to confidently undertake multiple projects A valid driving licence and comfortable covering a wide territory when needed Important information Reference number: 13394 FMC contact for this role: Adam Leeder
Dec 15, 2022
Full time
Our client, an established diagnostic imaging equipment supplier in Ireland, is now making waves across the UK and are seeking a Field Service Engineer to join their team around the Stevenage/North M25 area and ensure the operational excellence of their product portfolio. The company FMC Meditech has partnered with an exclusive radiology equipment provider who are blazing new trails across the UK healthcare market with their portfolio of medical imaging devices. This is an excellent opportunity to join a tight-knit, family-run team during an exciting phase of growth and demonstrate the far-reaching potential of their solutions. The role This role will involve the ongoing servicing, installation, maintenance and modification of our client's equipment across the East Midlands, both on-site and remotely. Liaising with customers will be a core focus - you'll plan and book your own maintenance visits to carry out preventative maintenance to maintaining uptime levels and providing first-time fix solutions when issues arise. You'll play a critical role in optimising the customer experience of the product portfolio and positioning our client as the partner of choice. Other requirements include: Building a network of established contacts Delivering quality service within timescales Ensuring rapid responses to customer queries Maintaining operational excellence for the customer base Achieving high levels of customer satisfaction Providing useful feedback concerning product acceptance and service Managing your workload and diary The requirements This role is suitable for candidates with an Electronic or Electrical HNC/HND qualification, apprenticeship, or degree. Other requirements include: Background of Field Service experience Strong knowledge of digital x-ray equipment Familiar with the installation of PC hardware and its associated software Outstanding information gathering and problem-solving skills Comfortable working individually and in a team environment Excellent communication skills (both written and verbal) Able to devise concise technical reports Responds well to feedback and personal development opportunities Organised and able to confidently undertake multiple projects A valid driving licence and comfortable covering a wide territory when needed Important information Reference number: 13394 FMC contact for this role: Adam Leeder
Supply Chain Officer - Medical Devices - Biomedical - South Birmingham Due to a Medical Devices company's recent growth, they are in need of a new Supply Chain Officer, in a newly created role, to help with the establishing and running of the companies Supply Chain, Quality Assurance and Operations duties. You will be based just South of Birmingham working alongside an established team of administrators, design engineers and scientists. While you develop in this role, you will gain more and more experience and skills to develop into more senior Operations roles in the future. As you will be working with highly technical individuals it would be essential that you have worked for a Medical Devices organisation in the past with a focus for new product development R&D while also producing and selling current medical devices products. In particular you will support the senior group leaders and project managers to insure the smooth running of important projects. It would be highly advantageous if your Medical Devices experience came from a Biomedical field, but not essential as other Medical Devices backgrounds will be considered. You will gain access to multiple projects across the business meaning you will learn a lot of things about new medical devices, scientific engineering and new products that will lead in the marketplace for years to come. As this is a new role, you will be taking duties that have previously been worked on the side by other people in the business. This means that you will be responsible for establishing the companies processes in the Supply Chain and Operations areas. Some of the key duties would include supplier management, inventory/stock management, QMS procedures, incoming goods management, supply chain reporting and other Supply Chain and Operations duties. It is expected that you will have a couple of years experience, at least, working for a Medical Devices company and hold a degree within an engineering, design, biomedical, science or another subject that led you into the Supply Chain or Operations field. In return you will be rewarded with an excellent salary, career growth, benefits package and bonus. I expect a lot of interest in this role, so if you are interested, I suggest you make an application now or risk missing out. For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on or make an application and one of our team at Newton Colmore Consulting will contact you. Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Science and Machine Learning fields.
Dec 07, 2022
Full time
Supply Chain Officer - Medical Devices - Biomedical - South Birmingham Due to a Medical Devices company's recent growth, they are in need of a new Supply Chain Officer, in a newly created role, to help with the establishing and running of the companies Supply Chain, Quality Assurance and Operations duties. You will be based just South of Birmingham working alongside an established team of administrators, design engineers and scientists. While you develop in this role, you will gain more and more experience and skills to develop into more senior Operations roles in the future. As you will be working with highly technical individuals it would be essential that you have worked for a Medical Devices organisation in the past with a focus for new product development R&D while also producing and selling current medical devices products. In particular you will support the senior group leaders and project managers to insure the smooth running of important projects. It would be highly advantageous if your Medical Devices experience came from a Biomedical field, but not essential as other Medical Devices backgrounds will be considered. You will gain access to multiple projects across the business meaning you will learn a lot of things about new medical devices, scientific engineering and new products that will lead in the marketplace for years to come. As this is a new role, you will be taking duties that have previously been worked on the side by other people in the business. This means that you will be responsible for establishing the companies processes in the Supply Chain and Operations areas. Some of the key duties would include supplier management, inventory/stock management, QMS procedures, incoming goods management, supply chain reporting and other Supply Chain and Operations duties. It is expected that you will have a couple of years experience, at least, working for a Medical Devices company and hold a degree within an engineering, design, biomedical, science or another subject that led you into the Supply Chain or Operations field. In return you will be rewarded with an excellent salary, career growth, benefits package and bonus. I expect a lot of interest in this role, so if you are interested, I suggest you make an application now or risk missing out. For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on or make an application and one of our team at Newton Colmore Consulting will contact you. Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Science and Machine Learning fields.
Position: Senior Supplier Development Engineer Location: Cambridgeshire Salary: £40,000 to £60,000 + Excellent Benefits / Prospects (including Relocation Assistance) If there is something stopping you from achieving all you re capable of, you ll relish a role with a company that will positively encourage you to be pro-active a real opportunity to release your true potential. The Company: Our Client, an innovative dynamic passionate manufactures minimal invasive next-generation robotic-assisted medical devices that are at the forefront of how surgical procedures are carried out. An award-winning company that plans to significantly disrupt the way surgery is performed for the benefit of millions of patients all around the world. Due to sustained continued expansion they now require a Senior Supplier Development Engineer to work with design groups to encourage Design to Cost is adequately considered as part of the design process. Other responsibilities include but are not limited to: Working closely with suppliers and design groups to facilitate smooth and speedy completion of DFM exchanges Design roll out, including equipment/process qualification for volume production Supplier process development to improve quality & consistency and reduce cost Sourcing and reviewing potential new component/assembly suppliers The Person: Candidates suitable for consideration should be able to provide evidence of the following: A Degree/HND in Engineering or be a Time Served Engineer with relevant experience. A knowledge/understanding of engineering concepts such as Design for manufacture, pre-production, industrial engineering, purchasing and procurement processes, integration, cost effectiveness, quality, and readiness for production Previous experience of working within Medical Device (ISO13485) experience (desirable) You will be self-motivated, have excellent communication skills both written and oral, be computer literate, and able to work as part of a team. The successful candidate will enjoy a salary of between £40,000 to £60,000 (DOE) + Excellent Benefits / Prospects (including Relocation Assistance) plus excellent prospects and an employment package that you would expect from a company that values its employees. Do you have the courage to take on this challenge?
Dec 01, 2022
Full time
Position: Senior Supplier Development Engineer Location: Cambridgeshire Salary: £40,000 to £60,000 + Excellent Benefits / Prospects (including Relocation Assistance) If there is something stopping you from achieving all you re capable of, you ll relish a role with a company that will positively encourage you to be pro-active a real opportunity to release your true potential. The Company: Our Client, an innovative dynamic passionate manufactures minimal invasive next-generation robotic-assisted medical devices that are at the forefront of how surgical procedures are carried out. An award-winning company that plans to significantly disrupt the way surgery is performed for the benefit of millions of patients all around the world. Due to sustained continued expansion they now require a Senior Supplier Development Engineer to work with design groups to encourage Design to Cost is adequately considered as part of the design process. Other responsibilities include but are not limited to: Working closely with suppliers and design groups to facilitate smooth and speedy completion of DFM exchanges Design roll out, including equipment/process qualification for volume production Supplier process development to improve quality & consistency and reduce cost Sourcing and reviewing potential new component/assembly suppliers The Person: Candidates suitable for consideration should be able to provide evidence of the following: A Degree/HND in Engineering or be a Time Served Engineer with relevant experience. A knowledge/understanding of engineering concepts such as Design for manufacture, pre-production, industrial engineering, purchasing and procurement processes, integration, cost effectiveness, quality, and readiness for production Previous experience of working within Medical Device (ISO13485) experience (desirable) You will be self-motivated, have excellent communication skills both written and oral, be computer literate, and able to work as part of a team. The successful candidate will enjoy a salary of between £40,000 to £60,000 (DOE) + Excellent Benefits / Prospects (including Relocation Assistance) plus excellent prospects and an employment package that you would expect from a company that values its employees. Do you have the courage to take on this challenge?
Position: Supplier Quality Engineer Location: Cambridgeshire Salary: £40,000 to £55,000 + Excellent Benefits / Prospects (including Relocation Assistance) If there is something stopping you from achieving all you re capable of, you ll relish a role with a company that will positively encourage you to be pro-active a real opportunity to release your true potential. The Company: Our Client, an innovative dynamic passionate manufactures minimal invasive next-generation robotic-assisted medical devices that are at the forefront of how surgical procedures are carried out. An award-winning company that plans to significantly disrupt the way surgery is performed for the benefit of millions of patients all around the world. Due to sustained continued expansion they now require a Supplier Quality Engineer to work within the routine quality group acting as an auditor and a liaison to suppliers over routine and quality issues. It will be your responsibility to develop a strong partnership with the Supplier Quality Assurance group and the procurement teams. Other responsibilities include, but are not limited to: Maintain good relationships with Supply Chain, Engineering, Manufacturing, and R&D departments. Facilitating corrective action and preventive actions aimed at addressing supplier quality issues, this includes ensuring appropriate investigations associated with product, supplier performance, and complaints Facilitating RoHS and REACH compliance Generating, reviewing and approving of supplier quality-related support documentation Reporting supplier performance and quality to management Reviewing supplier component documentation including 8Ds, dimensional and material reports for sign off acceptance The Person: Candidates suitable for consideration should be able to provide evidence of the following: A Degree/HND in Engineering or be a Time Served Engineer with relevant experience. Experienced quality professional with a broad knowledge of manufacturing processes & validation (IQ / OQ / PQ) Strong audit background / Lead auditor with ISO 13485 or CFR 820 experience. A thorough understanding of Quality Management Systems (ideally the requirements of ISO13485 and FDA 21 CFR part 820) Previous experience of working within Medical Devices (desirable) You will be self-motivated, have excellent communication skills both written and oral, be computer literate, and able to work as part of a team. The successful candidate will enjoy a salary of between £40,000 to £55,000 (DOE) + Excellent Benefits / Prospects (including Relocation Assistance) plus excellent prospects and an employment package that you would expect from a company that values its employees. Do you have the courage to take on this challenge
Nov 24, 2022
Full time
Position: Supplier Quality Engineer Location: Cambridgeshire Salary: £40,000 to £55,000 + Excellent Benefits / Prospects (including Relocation Assistance) If there is something stopping you from achieving all you re capable of, you ll relish a role with a company that will positively encourage you to be pro-active a real opportunity to release your true potential. The Company: Our Client, an innovative dynamic passionate manufactures minimal invasive next-generation robotic-assisted medical devices that are at the forefront of how surgical procedures are carried out. An award-winning company that plans to significantly disrupt the way surgery is performed for the benefit of millions of patients all around the world. Due to sustained continued expansion they now require a Supplier Quality Engineer to work within the routine quality group acting as an auditor and a liaison to suppliers over routine and quality issues. It will be your responsibility to develop a strong partnership with the Supplier Quality Assurance group and the procurement teams. Other responsibilities include, but are not limited to: Maintain good relationships with Supply Chain, Engineering, Manufacturing, and R&D departments. Facilitating corrective action and preventive actions aimed at addressing supplier quality issues, this includes ensuring appropriate investigations associated with product, supplier performance, and complaints Facilitating RoHS and REACH compliance Generating, reviewing and approving of supplier quality-related support documentation Reporting supplier performance and quality to management Reviewing supplier component documentation including 8Ds, dimensional and material reports for sign off acceptance The Person: Candidates suitable for consideration should be able to provide evidence of the following: A Degree/HND in Engineering or be a Time Served Engineer with relevant experience. Experienced quality professional with a broad knowledge of manufacturing processes & validation (IQ / OQ / PQ) Strong audit background / Lead auditor with ISO 13485 or CFR 820 experience. A thorough understanding of Quality Management Systems (ideally the requirements of ISO13485 and FDA 21 CFR part 820) Previous experience of working within Medical Devices (desirable) You will be self-motivated, have excellent communication skills both written and oral, be computer literate, and able to work as part of a team. The successful candidate will enjoy a salary of between £40,000 to £55,000 (DOE) + Excellent Benefits / Prospects (including Relocation Assistance) plus excellent prospects and an employment package that you would expect from a company that values its employees. Do you have the courage to take on this challenge
Site Name: UK - Hertfordshire - Ware RD Posted Date: May Principal Device Engineer Biopharm Process Development is a highly experienced Chemistry, Manufacturing and Controls (CMC) organisation accountable for delivering robust, cost effective and competitive products, and manufacturing processes spanning the full lifecycle of asset development from Discovery through commercialisation. These activities are delivered through state-of-the-art internal facilities as well as strategic external partners. Collectively, the team is accountable for CMC activities encompassing cell line development, cell culture/ microbial fermentation, purification development, and drug product/ device development. We also pioneer innovative technologies to improve robustness, reduce cost of goods, and improve the patient experience. Within Biopharm Process Development sits GSK's Device Engineering team; an in-house device development group charged with the delivery of robust, patient-centric devices that enable the effective delivery of novel pharmaceuticals. Job Purpose: We have an exciting opportunity for a Principal Device Engineer to join a multi-skilled team of Engineers and Scientists who work across all stages of the product and process development lifecycle, from concept design and selection through to the regulatory submission and commercial supply. You will be responsible for technical leadership of device development activities to support industrialisation of drug delivery platforms. You will be familiar with Quality by Design principles and developing programmes of work to build understanding of device designs and mechanisms.You should have awareness of in-silico modelling approaches which support device and mechanism understanding. Key Responsibilities: This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Providing technical leadership in order to industrialise drug delivery device platforms Work with internal and external project teams to establish the design space for drug delivery platforms and demonstrate robustness for commercial scale manufacture Design empirical test programmes to demonstrate device robustness across input specifications which meet regulatory expectations Engage with internal stakeholders to identify drug delivery technologies that enable the portfolio Engage externally to identify appropriate drug delivery technologies and perform due diligence / technical assessments Management of external suppliers to ensure development activities align with GSK expectations. Basic Qualifications/Experience: Degree qualified in Mechanical Engineering, Biomedical Engineering, Physics or related subjects. Excellent understanding of mechanical principles and systems Experience managing external manufacturing supply bases and design consultancies An understanding of the principles of design for manufacture and QbD Evidence of problem solving and experience running technical risk assessments Understanding of plastic injection moulding Strong time management/organisational skills Excellent written and verbal communication skills Performance driven, driving for results and success with a sense of urgency Evidence of team working skills and flexibility Awareness of quality and regulatory standards associated with device development Awareness of in silico modelling/design tools such as FEA, MATLAB, CFD, CAD Preferred Qualifications: Experience in Pharma or Medical Device development Experience with autoinjector development Why GSK? GSK is a place where outstanding people do amazing things. As a science-led global healthcare company, we exist to help people do more, feel better, live longer. This special purpose - along with our goal of being one of the world's most innovative, best performing and trusted healthcare companies - helps us attract some of the best and brightest minds in the world. We take pride in providing access to all and continually focus on our opportunity and obligation to do more to improve inclusion and diversity: for our people inside GSK; in the way we do business; and in the communities where we operate. We want our company to be a place where diversity of people and thought is valued everywhere and where we're all able to be ourselves and feel a sense of belonging. An inclusive organization where we all feel valued, engaged and supported, knowing that our work makes an important contribution to our mission.Reinforced by our clear values and expectations , it is part of our DNA. Together we achieve extraordinary things for our patients and consumers, who rely on us each and every day As a company driven by our values of Patient focus, Transparency, Respect and Integrity, we know inclusion and diversity are essential for us to be able to succeed. We want all our colleagues to thrive at GSK bringing their unique experiences, ensuring they feel good and to keep growing their careers. As a candidate for a role, we want you to feel the same way. As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class*(*US only). We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Please don't hesitate to contact us if you'd like to discuss any adjustments to our process which might help you demonstrate your strengths and capabilities. You can either call us on , or send an email As you apply, we will ask you to share some personal information which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially. 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Jun 02, 2022
Full time
Site Name: UK - Hertfordshire - Ware RD Posted Date: May Principal Device Engineer Biopharm Process Development is a highly experienced Chemistry, Manufacturing and Controls (CMC) organisation accountable for delivering robust, cost effective and competitive products, and manufacturing processes spanning the full lifecycle of asset development from Discovery through commercialisation. These activities are delivered through state-of-the-art internal facilities as well as strategic external partners. Collectively, the team is accountable for CMC activities encompassing cell line development, cell culture/ microbial fermentation, purification development, and drug product/ device development. We also pioneer innovative technologies to improve robustness, reduce cost of goods, and improve the patient experience. Within Biopharm Process Development sits GSK's Device Engineering team; an in-house device development group charged with the delivery of robust, patient-centric devices that enable the effective delivery of novel pharmaceuticals. Job Purpose: We have an exciting opportunity for a Principal Device Engineer to join a multi-skilled team of Engineers and Scientists who work across all stages of the product and process development lifecycle, from concept design and selection through to the regulatory submission and commercial supply. You will be responsible for technical leadership of device development activities to support industrialisation of drug delivery platforms. You will be familiar with Quality by Design principles and developing programmes of work to build understanding of device designs and mechanisms.You should have awareness of in-silico modelling approaches which support device and mechanism understanding. Key Responsibilities: This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Providing technical leadership in order to industrialise drug delivery device platforms Work with internal and external project teams to establish the design space for drug delivery platforms and demonstrate robustness for commercial scale manufacture Design empirical test programmes to demonstrate device robustness across input specifications which meet regulatory expectations Engage with internal stakeholders to identify drug delivery technologies that enable the portfolio Engage externally to identify appropriate drug delivery technologies and perform due diligence / technical assessments Management of external suppliers to ensure development activities align with GSK expectations. Basic Qualifications/Experience: Degree qualified in Mechanical Engineering, Biomedical Engineering, Physics or related subjects. Excellent understanding of mechanical principles and systems Experience managing external manufacturing supply bases and design consultancies An understanding of the principles of design for manufacture and QbD Evidence of problem solving and experience running technical risk assessments Understanding of plastic injection moulding Strong time management/organisational skills Excellent written and verbal communication skills Performance driven, driving for results and success with a sense of urgency Evidence of team working skills and flexibility Awareness of quality and regulatory standards associated with device development Awareness of in silico modelling/design tools such as FEA, MATLAB, CFD, CAD Preferred Qualifications: Experience in Pharma or Medical Device development Experience with autoinjector development Why GSK? GSK is a place where outstanding people do amazing things. As a science-led global healthcare company, we exist to help people do more, feel better, live longer. This special purpose - along with our goal of being one of the world's most innovative, best performing and trusted healthcare companies - helps us attract some of the best and brightest minds in the world. We take pride in providing access to all and continually focus on our opportunity and obligation to do more to improve inclusion and diversity: for our people inside GSK; in the way we do business; and in the communities where we operate. We want our company to be a place where diversity of people and thought is valued everywhere and where we're all able to be ourselves and feel a sense of belonging. An inclusive organization where we all feel valued, engaged and supported, knowing that our work makes an important contribution to our mission.Reinforced by our clear values and expectations , it is part of our DNA. Together we achieve extraordinary things for our patients and consumers, who rely on us each and every day As a company driven by our values of Patient focus, Transparency, Respect and Integrity, we know inclusion and diversity are essential for us to be able to succeed. We want all our colleagues to thrive at GSK bringing their unique experiences, ensuring they feel good and to keep growing their careers. As a candidate for a role, we want you to feel the same way. As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class*(*US only). 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Production Engineer - Medical Devices Your new company Our Clients works in the Medical devices manufacturing industry. Your new role As a Production engineer, you will work closely with the R&D Science, Tech, Quality and Operations teams and will use your previous practical experience of translating individual component designs & assemblies from proto-series through all stages and relevant testing processes to deliver the final production model. We are looking for a hands-on production engineer, fast-pace, innovative and passionate. You are logical and can develop clear action plans and communicate them with confidence to suppliers and internal teams. You have experience working within the Medical Device Manufacturing industry in a Mechanical Engineering focused role. Main responsibilities: To take initiative in the production planning of new scientific and consumer devices To help develop and produce single use IVD consumables To develop production lines, source production equipment and optimise production processes To work with closely with external manufacturers and suppliers To source new suppliers and OEM's To conduct tests and write reports To perform Risk Analysis, FMEA by applying ISO 14971 To design components and assemblies aided by CAD to produce 3D models, drawings and specifications To develop suitable techniques, and apparatus, for testing To design and conduct V&V testing protocols and procedures To maintain accurate and complete records of all findings To present findings to colleagues and work well with a diverse multi-skilled team What you'll need to succeed 3+ years working within a medical diagnostics or equivalent instrument company as a Mechanical Engineer, Production Engineer or Process Engineer working with mass-manufactured plastic parts MEng\/BEng or a closely related discipline, or equivalent research, industrial or commercial experience Knowledge \/ Experience Experience manufacturing medical device products that have a full DHF\/DMR\/DHR Experience using CAD software to design custom production equipment and associated jigs and fixtures Experience UV cure adhesives and associated production processes Experience in the design and assembly of prototype instruments and industrialization of said prototypes Experience of injection molding for fabrication of single-use items Extensive understanding of modern manufacturing processes Experience of working as part of an R&D team Experience of undertaking proof-of-concept studies Experience of working within a Medical device Quality Management System ISO 13485 Experience with preparation of reports and documents Desirable Experience with biomedical instrumentation Experience with biomedical sample handling and processing Experience of design for manufacturability (DFM) techniques Experience of design for Assembly (DFA) Experience with microfluidic components and production methods Experience with SolidWorks, OnShape or similar CAD package Experience with production programming, e.g. Labview, PLC's What you'll get in return Salary + Package What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk
Dec 07, 2021
Full time
Production Engineer - Medical Devices Your new company Our Clients works in the Medical devices manufacturing industry. Your new role As a Production engineer, you will work closely with the R&D Science, Tech, Quality and Operations teams and will use your previous practical experience of translating individual component designs & assemblies from proto-series through all stages and relevant testing processes to deliver the final production model. We are looking for a hands-on production engineer, fast-pace, innovative and passionate. You are logical and can develop clear action plans and communicate them with confidence to suppliers and internal teams. You have experience working within the Medical Device Manufacturing industry in a Mechanical Engineering focused role. Main responsibilities: To take initiative in the production planning of new scientific and consumer devices To help develop and produce single use IVD consumables To develop production lines, source production equipment and optimise production processes To work with closely with external manufacturers and suppliers To source new suppliers and OEM's To conduct tests and write reports To perform Risk Analysis, FMEA by applying ISO 14971 To design components and assemblies aided by CAD to produce 3D models, drawings and specifications To develop suitable techniques, and apparatus, for testing To design and conduct V&V testing protocols and procedures To maintain accurate and complete records of all findings To present findings to colleagues and work well with a diverse multi-skilled team What you'll need to succeed 3+ years working within a medical diagnostics or equivalent instrument company as a Mechanical Engineer, Production Engineer or Process Engineer working with mass-manufactured plastic parts MEng\/BEng or a closely related discipline, or equivalent research, industrial or commercial experience Knowledge \/ Experience Experience manufacturing medical device products that have a full DHF\/DMR\/DHR Experience using CAD software to design custom production equipment and associated jigs and fixtures Experience UV cure adhesives and associated production processes Experience in the design and assembly of prototype instruments and industrialization of said prototypes Experience of injection molding for fabrication of single-use items Extensive understanding of modern manufacturing processes Experience of working as part of an R&D team Experience of undertaking proof-of-concept studies Experience of working within a Medical device Quality Management System ISO 13485 Experience with preparation of reports and documents Desirable Experience with biomedical instrumentation Experience with biomedical sample handling and processing Experience of design for manufacturability (DFM) techniques Experience of design for Assembly (DFA) Experience with microfluidic components and production methods Experience with SolidWorks, OnShape or similar CAD package Experience with production programming, e.g. Labview, PLC's What you'll get in return Salary + Package What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk
About the role The Fab IT Engineer is responsible for the support of IT operations within a busy 24 x 7 semiconductor wafer fab facility. This role is particularly suited to an individual who enjoys handling multiple pieces of work at any given time, with the technical knowledge and hands on abilities, to undertake support of factory IT infrastructure activities. What you will do * Work on and manage the IT infrastructure within a busy semiconductor wafer fab * Build and issue devices to the factory. This can include Desktop Terminals, Stick PC's, Tablets * Maintain device security, which will include working with Equipment Engineers on patching Industrial Endpoints, not directly under the control of IT, as well as testing and releasing patches to IT issued devices * Working with IT infrastructure colleagues on managing zero-day vulnerability programmes * Support the installation and maintenance of serial network components, used for tool automation What you will need * Strong knowledge and proficiency in providing support for the Windows operating system, especially related to production critical clients (different versions of windows client) in the environment * Good Knowledge, Skills and Understanding of Microsoft technologies- Windows Server and Clients, Active Directory (GPO, OU, Groups), SCCM and should be capable of narrowing down and fixing issues relevant to the environment, using strong technical skills. * Good Knowledge of networking concepts, such as VLAN, DNS, DHCP * Experienced using SCCM Management (Configurations, deployment of security patches, health checks, inventory reports, etc) * System debugging (event logs, GPResult, perfmon, process dumps) * Proficiency in creating documentation for end users * Creating plans by coordinating with multiple teams to meet timelines and deliver service improvements in line with plans * Experience in Power shell, with the ability to develop and automate processes * Excellent verbal and written communication skills * Proven problem-solving skills, attention to detail Why work for us? * Competitive compensation and benefits packages * Flexible working scheme * Excellent training and development opportunities * Annual / paid leave and pension plan * Hybrid working policy for select roles: 50/50 office and home working * Recognition reward schemes * Flexible talent and leadership programs * On-site medical centre and staff canteen * Cycle-to-work scheme * Range of employee discounts (including travel, health insurance, high street and online retailers) * Sport and social clubs * Good relocation packages About the team Our Power MOSFET business line is one of the top suppliers of high-quality power MOSFETs to the Automotive industry as well as a major player in providing general purpose MOSFETs to the computing, industrial and consumer markets
Dec 05, 2021
Full time
About the role The Fab IT Engineer is responsible for the support of IT operations within a busy 24 x 7 semiconductor wafer fab facility. This role is particularly suited to an individual who enjoys handling multiple pieces of work at any given time, with the technical knowledge and hands on abilities, to undertake support of factory IT infrastructure activities. What you will do * Work on and manage the IT infrastructure within a busy semiconductor wafer fab * Build and issue devices to the factory. This can include Desktop Terminals, Stick PC's, Tablets * Maintain device security, which will include working with Equipment Engineers on patching Industrial Endpoints, not directly under the control of IT, as well as testing and releasing patches to IT issued devices * Working with IT infrastructure colleagues on managing zero-day vulnerability programmes * Support the installation and maintenance of serial network components, used for tool automation What you will need * Strong knowledge and proficiency in providing support for the Windows operating system, especially related to production critical clients (different versions of windows client) in the environment * Good Knowledge, Skills and Understanding of Microsoft technologies- Windows Server and Clients, Active Directory (GPO, OU, Groups), SCCM and should be capable of narrowing down and fixing issues relevant to the environment, using strong technical skills. * Good Knowledge of networking concepts, such as VLAN, DNS, DHCP * Experienced using SCCM Management (Configurations, deployment of security patches, health checks, inventory reports, etc) * System debugging (event logs, GPResult, perfmon, process dumps) * Proficiency in creating documentation for end users * Creating plans by coordinating with multiple teams to meet timelines and deliver service improvements in line with plans * Experience in Power shell, with the ability to develop and automate processes * Excellent verbal and written communication skills * Proven problem-solving skills, attention to detail Why work for us? * Competitive compensation and benefits packages * Flexible working scheme * Excellent training and development opportunities * Annual / paid leave and pension plan * Hybrid working policy for select roles: 50/50 office and home working * Recognition reward schemes * Flexible talent and leadership programs * On-site medical centre and staff canteen * Cycle-to-work scheme * Range of employee discounts (including travel, health insurance, high street and online retailers) * Sport and social clubs * Good relocation packages About the team Our Power MOSFET business line is one of the top suppliers of high-quality power MOSFETs to the Automotive industry as well as a major player in providing general purpose MOSFETs to the computing, industrial and consumer markets
Job description: WHAT TO EXPECT You will be expected to take a prominent role for your area of specialism, across one or more of the cyber security delivery phases such as the development of cyber security requirements for a critical system or the software verification of and testing of these systems. As well as this, you will be expected to develop industry standards and strategies in your area of specialism, prominent their deployment in the business. You will be expected to engage with suppliers to establish vulnerabilities associated with their systems and define a joint approach to safeguarding these systems. You will need to represent the department in wider business discussions and be hands-on with software development teams. This will have considerable experience through verification testing, including potentially penetration testing and show clear traceability through standards, process definition and technical documentation. WHAT YOU'LL NEED As a Cyber Security Subject Matter Expert, you will be in charge of a wide variety of tasks, including developing business strategies in your area of specialism, prominent their deployment into the business on a worldwide scale, applying system thinking and engineering knowledge to aid the delivery of secure vehicle systems and prominent internal and external certification activities, audits, and cybersecurity standards reviews. This role will include identifying and eleviating technical risks and collaborate with developers to resolve technical issues whilst ensuring the maintenance of departmental and company standards & procedures. You will monitor and respond to threats identified from a range of sources including analysis of vehicle systems, disclosures and theoretical analysis. Whilst ensuring continuous improvement through effective lessons learned, knowledge capture and process development compliant with standards such as ISO21434. Knowledge, Skills and Experience Essential: * Experience and track record of delivery in a field relevant to the role. * Qualified to degree level in a relevant discipline, or equivalent experience. * An ability to think logistically and creatively with a commitment to quality and outstanding results. * Able to carry out detailed work against security attributes, and able to constructively assess others' work. * Excellent written and verbal communication skills; ability to confer complex technical and procedural topics in a clear and concise form, confidently presenting with senior stakeholders. Desirable: * Prior experience relating to the development of safety-critical software. * Expertise in requirements management and ALM systems, e.g. IBM Rational DOORS, RTC, JIRA or similar. * Automotive experience is preferred, but we are also keen to hear from candidates with knowledge in other relevant fields, e.g. aerospace, defence, IT, industrial controls, medical devices or similar.
Nov 30, 2021
Full time
Job description: WHAT TO EXPECT You will be expected to take a prominent role for your area of specialism, across one or more of the cyber security delivery phases such as the development of cyber security requirements for a critical system or the software verification of and testing of these systems. As well as this, you will be expected to develop industry standards and strategies in your area of specialism, prominent their deployment in the business. You will be expected to engage with suppliers to establish vulnerabilities associated with their systems and define a joint approach to safeguarding these systems. You will need to represent the department in wider business discussions and be hands-on with software development teams. This will have considerable experience through verification testing, including potentially penetration testing and show clear traceability through standards, process definition and technical documentation. WHAT YOU'LL NEED As a Cyber Security Subject Matter Expert, you will be in charge of a wide variety of tasks, including developing business strategies in your area of specialism, prominent their deployment into the business on a worldwide scale, applying system thinking and engineering knowledge to aid the delivery of secure vehicle systems and prominent internal and external certification activities, audits, and cybersecurity standards reviews. This role will include identifying and eleviating technical risks and collaborate with developers to resolve technical issues whilst ensuring the maintenance of departmental and company standards & procedures. You will monitor and respond to threats identified from a range of sources including analysis of vehicle systems, disclosures and theoretical analysis. Whilst ensuring continuous improvement through effective lessons learned, knowledge capture and process development compliant with standards such as ISO21434. Knowledge, Skills and Experience Essential: * Experience and track record of delivery in a field relevant to the role. * Qualified to degree level in a relevant discipline, or equivalent experience. * An ability to think logistically and creatively with a commitment to quality and outstanding results. * Able to carry out detailed work against security attributes, and able to constructively assess others' work. * Excellent written and verbal communication skills; ability to confer complex technical and procedural topics in a clear and concise form, confidently presenting with senior stakeholders. Desirable: * Prior experience relating to the development of safety-critical software. * Expertise in requirements management and ALM systems, e.g. IBM Rational DOORS, RTC, JIRA or similar. * Automotive experience is preferred, but we are also keen to hear from candidates with knowledge in other relevant fields, e.g. aerospace, defence, IT, industrial controls, medical devices or similar.