As Senior Device Engineer, reporting to one of the Engineering Team Leaders or to a Project Technical Lead, you will play a key role in ensuring our combination products are safe, effective, and compliant with global standards. You will apply best-practice engineering principles, Design Controls, and Safety Risk Management to guide products from concept through to production. You will collaborate closely with multidisciplinary teams from across Teva, including the CPD team of laboratory scientists, human factors engineers, and project managers, as well as the wider-Teva network including formulation scientists, regulatory experts, marketing and manufacturing from Teva’s global sites. Your expertise in manufacturing technologies — such as plastic injection moulding — will be vital in preparing device designs for seamless transfer into production. You will bring creativity and problem-solving skills to tackle complex engineering challenges, while contributing to the evolution of our departmental systems and influencing best practices across the team.
Responsibilities
* Support the engineering design and development of drug delivery devices across various stages of development, including early research, design verification and validation, and lifecycle management.
* Ensure that products in your care are reliably engineered through appropriate design, analysis, and testing methodologies; comprehensively specified, ready to be verified, and provide objective evidence of compliance.
* Document compliance with CPD's Quality Management System.
* Lead or support Safety Risk Management activities, including hazard identification, risk analysis and evaluation through FMEAs, and support to the MS&T function in process risk assessments.
* Lead or support technical design reviews to assess design robustness, safety, and documentation quality compliance.
* Lead or support investigations to identify root causes of device-related issues using techniques such as Fault Tree Analysis and Design of Experiments.
* Contribute to continuous improvement of departmental processes, including SOPs, guidelines, templates, and the introduction of new software tools.
* Mentoring and coaching capabilities, with the ability to support and guide junior colleagues as required.
* Responsible for the management of externally sourced engineering services, including oversight of budgets, timelines, and risk.
* Domestic and international travel may be required (approximately 10%) to support project activities, including visits to suppliers, Teva manufacturing sites, and other stakeholders.
Qualifications
* Bachelor's degree (or higher) in Engineering, Scientific, or other relevant technical discipline.
* Proven experience in the design, manufacture, and lifecycle management of medical devices or combination products from concept through to commercialisation (preferred), or equivalent expertise from a relevant regulated industry.
* Demonstrable high level of independence in executing engineering tasks, with minimal supervision; proactively identifies additional activities and seeks peer support when appropriate.
* Training in Design Controls, medical device Safety Risk Management, and European Medical Device Directive/Regulations (preferred).
* Familiarity with statistical methods relevant to design input definition, verification and validation testing, including determination of sample sizes proportionate to risk.
* Strong 3D spatial awareness and ability to visualise concepts, mechanisms, and assemblies.
* Working knowledge of SolidWorks 3D CAD software (preferred).
* Are you: able to influence and educate peers and stakeholders; confident in professional judgement and decision-making.
* Bringing strong analytical skills with the ability to assess mechanisms and systems from a first-principles engineering perspective.
* Comfortable operating in dynamic environments, with the ability to adapt to change, manage uncertainty, and respond flexibly to evolving conditions.
* Excellent verbal and written communication skills, including the ability to produce high-quality engineering documentation.
About Teva CPD Abbots Park
Join Teva's Combination Products & Devices (CPD) R&D Team - Shaping the Future of Drug Delivery. At Teva's CPD team in Abbots Park, Runcorn, we’re pioneering the development of advanced needle-based injection devices and cutting-edge technologies to deliver our portfolio of Small Molecule and Generic medicines. From Pre-Filled Syringes (PFS) to Autoinjectors and Pen Injectors, our diverse device portfolio supports both generic and specialty products across key therapeutic areas including Neuroscience, Immunology, and Endocrinology. Within CPD Abbots Park, our work is organised into three product technology clusters, each broadly focused — though not exclusively — on a specific subset of injection devices:
* Cartridges & Pen Injectors
* Autoinjectors (AI)
* Pre-Filled Syringes & Safety Systems (PFS)
We support our people through every stage of their journey with us. Our flexible reward platform puts you in control, empowering you to tailor your benefits to fit your lifestyle, priorities, and what matters most to you. With 25 days of annual leave that grows with your service, the flexibility to purchase additional days, and two dedicated volunteering days each year, your time off is truly yours to enjoy, recharge, and give back. We prioritise your health with private medical insurance, life assurance, critical illness cover, and income protection. Whether you’re growing your family or pursuing new adventures, our enhanced maternity and paternity leave, sabbaticals, and hybrid working policies are here to support you through life’s most meaningful moments. Financial wellbeing matters too, which is why we offer an enhanced pension scheme, access to a discount store, and free financial coaching through Bippit. To help you grow with confidence, we offer a structured training and development programme tailored to your role and department, equipping you with the tools, knowledge, and support you need to thrive.
Already Working @TEVA? #TJ If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
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