Manual Software Tester jobs at Philips in United Kingdom, Rushmoor

Your role:

• Supporting the manual software Testing for EC Pro products: including software testing, Defect management, software test lifecycle maintenance activities and automation.

• Contributing to design and development of Test Protocols

• Tests functional and non-functional requirements both manual and/or automated

• Contributing to rigorous engineering based in a scientific approach to design reviews and verification testing aiming to meet customer needs with a strong focus on risk and safety.

• Maintaining team relationships and working with automation counterparts in EC

• Following quality procedures in line with engineering processes needed to attain and maintain medical device regulatory approvals.

Be sure to ask you recruiter about the compensation package on offer

How we work together

• We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. This role is an office role in Farnborough, Hampshire..

You're the right for the role if you have:

• A Bachelor of Engineering or Computing degree or equivalent iin an appropriate engineering/technical discipline.

• Good knowledge and experience of software verification/validation with Behaviour Driven Development and/or Test-Driven Development experience.

• Proven experience in a manual testing role, formulating Test Strategies, Test Plans & Procedures

• Experience in Development and Continuous Integration tools such as ADO, Azure DevOps....etc. would be beneficial;

As the studio manager, you’ll help launch and manage a flexible studio space that hosts video recordings, live press interviews and a remote production video set. By standardizing our in-house capabilities, you’ll help meet our existing video production needs and help us be ready to meet the new demands of Philips’ Communications & Brand function.

Objectives for the role

• Manage an on-site studio and editing room, ensuring the smooth running of the production teams’ workflow and administrative processes.
• Produce (and provide editorial guidance for others) in scripting, storyboarding, filming, producing, editing and finalizing videos.
• Assess the studio’s occupancy rate, creating reports and recommending or carrying out continuous improvements and managing equipment inventory.
• Stay up-to-date on the latest industry trends in video production and usage, and platform changes, integrating new approaches and technologies.
• Collaborate closely with teams in Comms & Brand and across the company, fostering positive relationships at every level of leadership.

Your role

• Produce and direct live and digital events (internal and external).
• Film, edit and deliver on-brand and polished videos to meet stakeholder requirements.
• Oversee day-to-day productions at the studio to ensure the highest quality content is being produced, andaudit and review filmed content to ensure high quality levels are achieved.
• Manage suppliers and, when needed, on-site technical crews
• Serve as first point of contact for anyone using the studio and editing room (presenters, business stakeholders, executives, customers, etc.).
• Attend briefing and planning sessions, actively taking part in discussions about filming projects to offer advice and support.

You are a right fit if you have the following:

• Bachelor’s/master’s degree (or equivalent) in communications, marketing or a related area.
• Eight years’ experience working in film/video, including production of videos of various kinds.
• At least five years’ professional experience in production within a multinational company, studio, and/or production company.
• Demonstrated track record in creating content specific to health technology.
• Proven ability to maneuver in matrix organizations and interface with executives.
• Excellent project management skills, and the ability to manage several tasks simultaneously, while remaining calm under pressure.
• Strong communication and interpersonal skills.
• Innovative and creative approaches to challenges.
• Sharp attention to detail and ability to work at pace.
• Curiosity, energy and a pro-active and results-oriented approach.

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Your role:

• Embedded Software Development: Lead the design, development, and sustainment of embedded software in collaboration with cross-functional teams and external stakeholders.

• System and Software Support: Provide technical support for customer and product investigations, defect resolution, lifecycle maintenance, and feature enhancements.

• Process and Documentation: Contribute to software process controls, design documentation, risk management activities, and CAPA processes.

• Requirements and Architecture: Translate customer and business requirements into robust embedded systems and software architectures, ensuring alignment with product goals.

• Technical Analysis: Interpret technical documentation such as circuit diagrams and datasheets, and decompose complex designs into integrated electronic, mechanical, and software subsystems.

• Engineering Excellence: Apply rigorous, science-based engineering practices to design reviews, decision-making, problem solving and verification testing, with a strong focus on risk management and safety.

• Regulatory Compliance: Ensure adherence to relevant medical device standards (e.g., IEC 60601-1, IEC 60601-2-xx, IEC 62304) and quality procedures necessary for regulatory approvals.

• Cross-functional Collaboration: Foster strong working relationships across R&D, PMO, product management, operations, regulatory, and quality teams, with a particular focus on coordination with principal software subcontractors.

• Technical mentorship and guidance: Operate as a technical leader within the team, providing guidance, support and oversight as appropriate

• Be sure to speak to your recruiter about all the salary, bonus and benefits on offer.

How we work together

• We believe that we are better together than apart. For this role, this means working in-person at least 3 days per week in our Farnborough, Hampshire office.

You’re right for this role if:

• You have an Engineering degree (or equivalent) in a relevant technical specialty.

• Your experience has been ideally gained in medical devices, but would also consider other regulated industries (pharma, aerospace, automotive).

• You have experience leading software development in an embedded Linux environment.

• You are experienced in embedded electronic / software systems (including comms technologies like TCP/IP, ethernet, USB, WiFi, Bluetooth), software design, object-orientated design, APIs, software quality, IEC 62304.

• You have worked in product development within an ISO 14971 quality system (preferably including experience of product approvals for EU-MDD, EU-MDR and FDA).

• You have a flexible attitude, with a willingness to accept and drive change, work within a dynamic environment

• You are a clear and concise communicator, with the ability to present to a broad range of stakeholders

For more information, read our Inclusion and Diversity Policy and, to know more about your Human Rights, we encourage you to view this .

Senior Software Architect (Embedded)

Your role:

• Supporting the decision making around systems and software for EC Pro products: including support for customer investigations, software defect investigations, software lifecycle maintenance activities and projects enhancing system and software features and behavior. Providing supporting input to risk management, software process controls, software specifications and software related CAPAs.

• Utilizing a broad experience of medical devices contributing to the architecture of EC Pro product road-mapping, platform development activities, new product advanced development projects and the design of new products.

• Contributing to complex development tasks; in relation to translating customer and business requirements into embedded electronic systems and software architecture and requirements.

• Interpreting requirements, reading electronic circuit diagrams, data sheets and understanding the approach to decomposing designs into effective electronic, mechanical, and software sub-systems.

• Contributing to rigorous engineering based in a scientific approach to decision making, design reviews and verification testing aiming to meet customer needs with a strong focus on risk and safety. Contributing to the application of relevant medical device standards applied to EC products including IEC 60601-1, associated IEC 60601-2-xx particular standards and IEC 62304. Following quality procedures in line with engineering processes needed to attain and maintain medical device regulatory approvals.

• Maintaining team relationships and working technically within the functions in the local business, software related suppliers and with counterparts in EC; in particular working in R&D engineering with staff in PMO, product management, operations, regulatory and quality. A significant focus will include interaction with the principal software sub-contractors.

• From competitive salary and performance bonus to family friendly policies, flexible benefits and access to Philips University, a career at Philips comes with all sorts of wonderful benefits. Be sure to speak to your recruiter about all the benefits on offer.

How we work together

• We believe that we are better together than apart. For this role, this means working in our Farnborough, Hampshire office at least 3 days per week.

You're right for this role if:

• You have an Engineering degree (or equivalent) in a relevant technical specialty.

• Your experienced in embedded electronic / software systems (including communications technologies, such as TCP/IP, ethernet, USB, WiFi, Bluetooth), software design, object-orientated design, APIs, software quality, IEC 62304.

• You have worked in product development within an ISO 14971 quality system (preferably including experience of product approvals for EU-MDD, EU-MDR and FDA).

• You would describe yourself as having a flexible attitude, with a willingness to accept and drive change, work with ambiguity & frequent change and have a rigorous approach to problem solving

• Ability to present, write and review engineering documents created by peers.