OSLER DIAGNOSTICS is looking for employees for positions:
management accountant
Working hours
full-time
Salary
salary
Requirements
osler is a fast-paced, dynamic, and intellectually stimulating business to work for
you will be confident, hard-working, and ambitious
you will have the capability to operate independently, problem solve, innovate, and identify and deliver improvements in an exciting yet sometimes ambiguous environment
you will be able to use your financial experience in order to turn the goals of the business into a commercial reality, and you will be a confident communicator with the gravitas to engage with and influence at all levels of the business
Responsibility
employment Status: Full Time, Perm
practice: Finance
location: Oxford
liaise with the external audit and tax teams to resolve queries effectively
prepare monthly financial statements and commentary of performance against forecast, to deliver high quality information to the Head of Finance, Chief Financial Officer, the Board of Directors, and the shareholders
prepare the UK GAAP financial statements, complete with supporting disclosure information
prepare high-quality, accurate and timely monthly management accounts and balance sheet reconciliations
prepare corporate tax, R&D tax credit, VAT, PAYE, P11D and PSA computations and assist with the reporting of all relevant information to the HMRC
senior systems engineer
Working hours
full-time
Language
english
Salary
salary
Responsibility
create and maintain system and subsystem requirements, including change control using Codebeamer X
plan, coordinate and perform risk management activities in accordance with IVD regulatory standards, throughout the product development lifecycle
provide guidance and support to other functional areas on the relevant risk management processes and procedures
lead appropriate Cross Functional teams to review design changes and their potential impact on Risk management documentation
plan, design, execute and report on system and subsystem level verification testing
job Title: Senior Systems Engineer
employment Status: Full Time, Perm
practice: Systems
process engineer
Working hours
full-time
Salary
salary
Responsibility
challenge and/or escalate non-conformance or contrary behaviours where known
set objectives, and schedule work package deliverables, ensuring appropriate and relevant division of work & responsibility across a multi-disciplinary technical team
job Title: Senior Process Engineer
assemble and circulate reports to document project status
employment Status: Full Time, Perm
in all areas within own remit, foster a workplace culture that prioritises the health, safety, and well-being of its employees, demonstrating a commitment to communicating, improving and adhering to safety policies
act as a coach and mentor to colleagues improving knowledge, competence, and capability, of individuals and teams
in conjunction with Product Development Lead, determine process engineering scope and develop work plans for complex technical projects to achieve defined objectives and outcomes
software test engineer
Working hours
full-time | Permanent
Salary
salary
Responsibility
drive of all aspects of software test engineering including functional, GUI
integration, system, and regression testing
reviewing and recommending new test practices that will enable the team to
maximise testing efficiency
collaborate with software development leads to jointly drive forward the quality of our
software
provide appropriate test reports to the leadership team, in a timely manner
reviewing and signing off requirements and test cases
Requirements
knowledge of git and platforms such as Jira and Confluence
an ability to rapidly understand complex technical requirements and derive test cases from these requirements
development of software to medical device standards
formulation of detailed test cases that provide comprehensive coverage of software requirements
test Driven Development
development of test scripts to automate test cases in scripting languages
cloud technologies, in particular using RESTful APIs
manual execution of test cases
software engineer
Responsibility
delivery of high-quality applications on the Android platform
ability to quickly understand and contribute to an existing codebase
UI design and implementation, and an ability to work with UX designers
use of Java language for Android, associated tools, and test frameworks
delivery of detailed requirements and design documents
integrating applications via APIs
ability to communicate complex technical issues clearly to other team members including Developers, Test Engineers, Product Owners, and System Integration
skills & Experience
systems engineer
Working hours
full-time
Salary
salary
Responsibility
support design and development of Osler products through integration of software, electrical and mechanical subsystems as part of overall system architecture
contribute towards investigations related to system level failure modes and implementation of identified solutions
support development, deployment and continuous improvement of lab based test equipment
assess new technologies related to company innovation strategy
Requirements
essential
adept at problem analysis and solving in complex electromechanical systems including ability to develop test methods / protocols to support investigations
working knowledge of electronics, software and mechanical engineering domains
hands-on experimentalist with attention to detail
strong knowledge of Microsoft tools
ability to communicate complex topics to non-technical audience
good collaborator that can communicate with wide range of stakeholders from different disciplines
prioritization with minimum guidance in fast paced environment
senior mechanical design engineer
Working hours
full-time
Salary
salary
Responsibility
engineering design analysis
part and sub assembly verification testing and reporting
detailed design and specification of components and assemblies for manufacture of a complex electro-mechanical Instrument and/or moulded consumable in the medical domain
Requirements
essential skills/experience
knowledge of materials & moving mechanisms/actuators, design of & integration of electro-mechanics such as motors, heaters, sensors, switches, slides, solenoids etc
confident 3D CAD practitioner
knowledge and experience of mass manufacturing techniques, especially sheet metal structures, cast parts & plastics injection moulding
hands On root cause analysis, testing, problem solving, Design for Cost
design of complex injection moulded plastic components to approved tool and volume production
desirable skills/experience
demonstrable Design for Manufacture/Assembly/Service/Cost experience - mid to high volume
facilities manager
Working hours
full-time | Permanent
Responsibility
contribute to an effective Business Support Team in order to develop harmonious and inter-dependant relationships across technical and non-technical teams
deliver internal communications commensurate with the above areas of responsibility
oversee the proactive management and maintenance of the office space as well as having responsibility for the overall building management budget, owned by the CFO
manage the front-of-house team to support the above activities
lead on planning and project managing developments in our facilities as we evolve and grow; liaising with external contractors and service providers so that we are set up to succeed
oversee vendor management for key office supplies such as food and drink, stationery and more; as well as the proactive maintenance of office assets, PAT testing and other related activities
oversee the business support and stores teams when welcoming guests, arranging meetings and receiving deliveries. Provide the 'personal touch' when looking after high-profile visitors, including investors and board members
the EHS element of the role may be to a greater or lesser extent depending on your experience
senior engineer
Working hours
full-time
full-time | Permanent
Salary
salary
Responsibility
ensuring Osler's medical device component suppliers are appropriately qualified, managed and monitored throughout the product lifecycle
work collaboratively with the product development team to provide quality assurance in design and development of medical devices
collect, analyse, monitor and report on supplier quality metrics and key performance indicators associated with supplier capability and component quality
build and maintain effective supplier relationships, manage supplier feedback and coordinate resolution of supplier related non-conformances and CAPAs
identify and address gaps related to all aspects of product Quality and compliance for the design and development
ensure component qualification methods of suppliers are aligned with Osler's quality standards, medical device regulations and industry best practices
design appropriate inspections to verify required quality standards are met
job Title: Senior Quality Assurance Engineer
Requirements
essential
experience of writing, reviewing and approving design and development documentation and processes
experience working within an ISO13485 certified QMS which is aligned to FDA Quality System Requirements, with senior responsibilities and process ownership
experience of working within and of maintaining an ISO 13485 certified QMS
desirable skills/experience
experience in dealing with global suppliers providing business critical components/services
experience of participating in and supporting regulatory audits
experience of working with multidisciplinary development teams
senior design engineer
Working hours
full-time | Permanent
Language
english
Salary
salary
Responsibility
author Design Verification plans, protocols and reports and support technical teams to create verification documentation
develop and manage complex product build and test schedules to ensure efficient use of materials and resources both internally and externally
drive and coordinate Design Verification activities across product system, including mechanical, electrical and software technical areas, in accordance with IVD regulatory standards
this is a hands-on role, working collaboratively with development scientists and engineers to determine the methods and evidence required to verify that a product design meets its requirements
gatekeeper for Design Verification – Ensure product design requirements are clearly defined and verifiable; Ensure design outputs are correctly specified and documented to support verification; Ensure that the required design verification deliverables are created to support completion of the design verification stage
Requirements
essential
experience working within an ISO 13485 QMS in medical device / IVD product development
coordination and facilitation across quality, regulatory and multi-disciplinary technical teams
strong technical documentation reading and writing skills, including presenting of data in meaningful and relevant formats
experience working with complex electromechanical products and awareness of test methods for mechanical, electrical and software requirements
desirable
experience in leading Design Verification activities for IVD / medical devices
excellent metrology knowledge including performing Gauge R&R studies/MSA