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Neil Cammish

Technical Director

Consulting engineer: drug/device product development, design, industrialisation, risk management.

Manchester, United Kingdom

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Neil Cammish's Email Addresses & Phone Numbers

Neil Cammish's Work Experience

International Device Solutions

Technical Director

August 2014 to Present


Device Consultant / Subject Matter Expert

August 2014 to Present

Basel Area, Switzerland

Teva Pharmaceuticals

Global Device Technology Manager

February 2012 to August 2014

Neil Cammish's Education


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About Neil Cammish's Current Company

International Device Solutions

Independent and non exclusive consultant and subject matter expert for global pharmaceutical and medical device companies. Specialises in drug delivery device (combination, disposable, reusable and standalone 510(K)/CE) development and industrialisation. I manage design input requirements from patient needs through development, proof of concept and robustness. I also author and manage design outputs and verification and validation activities,...

Frequently Asked Questions about Neil Cammish

What company does Neil Cammish work for?

Neil Cammish works for International Device Solutions

What is Neil Cammish's role at International Device Solutions?

Neil Cammish is Technical Director

What is Neil Cammish's personal email address?

Neil Cammish's personal email address is ne****[email protected]

What is Neil Cammish's business email address?

Neil Cammish's business email address is n****[email protected]

What is Neil Cammish's Phone Number?

Neil Cammish's phone +44 ** **** *206

What industry does Neil Cammish work in?

Neil Cammish works in the Medical Devices industry.

About Neil Cammish

📖 Summary

Chartered engineer and fellow of the institute of engineering designers. Co-located between the UK and Switzerland, working internationally on global drug delivery device projects. I have diverse experience of creating, innovating and executing complex engineered solutions, based upon realistic, pragmatic and capable engineering design and manufacturing management. As a qualified professional engineering design practitioner, mechanical and manufacturing engineer, and experienced technical director of complex global operations, I can analyse systems - device or process, and quantify risk (to user or patient and/or commercial). I then often work diplomatically and sympathetically with all stakeholders in a global team - from a factory floor to the boardroom in order to reduce or mitigate unacceptable risk. I overcome technical challenges through practical and capable (often simple!) engineering design change or improvement solutions and verify, theoretically and empirically before validating the outcome is fit for purpose/intended use. I challenge experts and ensure work is carried out according to international standards and/or within regulatory boundaries. I have extensive experience of engineering, process and design, deep dive technical analysis and manufacturing trouble shooting. Late stage, often innovative design or process change management is a particular strength. I lead and add rigour to technical projects for the successful design and industrialisation of high volume precision manufactured medical devices, safety critical and lifesaving civil and military equipment, high value consumer products/hand held devices at an international level. I specialise in autoinjector and pen injector drug/device combination products, assessment, troubleshooting and due diligence activities . Providing device solutions internationally with quality by design. Please feel free to get in touch to see how I can help improve design and reduce risk in your critical project.Technical Director @ Independent and non exclusive consultant and subject matter expert for global pharmaceutical and medical device companies. Specialises in drug delivery device (combination, disposable, reusable and standalone 510(K)/CE) development and industrialisation. I manage design input requirements from patient needs through development, proof of concept and robustness. I also author and manage design outputs and verification and validation activities, submission documentation, quality and risk management systems compliant with ISO 14971. My core skill is deep technical assessment/due diligence during development and late stage change management, trouble shooting, root cause analysis, life cycle management or recall solutions via pragmatic innovation and project architecture. I help companies minimise risk to purchase, deliver and maintain safe and successful products to market in the shortest time possible. Often this means working in collaboration with and challenging internal partners, external international design authorities, patent holders and/or the CMO(s) to fix problems, analyse, quantify and minimise risk and add value and for all parties. From August 2014 to Present (1 year 5 months) Device Consultant / Subject Matter Expert @ Providing services via my company, International Device Solutions as a retained and preferred supplier for the development, specification, analysis, trouble shooting and risk management of drug/device combination products for the world's number 1 in biotech alongside and with Genentech. Cooperation with, and technical management of global medical device technology suppliers for safe and technically viable drug delivery solutions on time. From August 2014 to Present (1 year 5 months) Basel Area, SwitzerlandGlobal Device Technology Manager @ Management, technical oversight and review, generation (IP), implementation and industrialisation of global medical device technology for sterile drug delivery. I worked with IP owners, device designers and suppliers worldwide, trouble shooting and managing solutions. I worked on and was responsible for multiple parallel projects to deliver Teva's broad generic, innovator, bio and bio similar portfolio for a wide spectrum of patient groups and from unmet needs through design and manufacture, verification and validation to life cycle management for delivery devices and drug/device combination products. In summary, technical ownership, design oversight, supplier education, challenge and management to add quality and scientific/engineering rigour for primary drug packaging, safety and injection devices for drug products in development such as Exenatide, Epinephrine (Epipen) and Sumatriptan, those in production such as Copaxone and standalone 510(k)/CE type devices such as CSYNC. From February 2012 to August 2014 (2 years 7 months) Principal Engineer (Injectables) @ Responsible for the design, industrialisation and commercial high volume manufacture of bespoke disposable autoinjector drug/device combination products for biotech & pharmaceutical customers and off-the-shelf and customisable platform disposable autoinjectors. From February 2008 to February 2012 (4 years 1 month) Senior Design Engineer @ Responsible for late stage design improvements and industrialisation (scale up) of a Dry Powder Inhaler for a chronic condition. Led and reported on critical device investigations and device improvement packages from concept/innovation stage, IP generation etc through to integration with high volume automation and implementation. Liaison and management of high profile design consultancies and advanced analysis and research both internal and external. Improved robustness of device and compliance with FDA regulations in order to enable clinical trials (PK and Phase III). From 2006 to 2008 (2 years) Senior Design Engineer @ Lead engineer of a security cleared team tasked with the design and production of the General Service Respirator program for the UK armed forces. Close management of international suppliers, liaison and supervision of specialised risk management consultants as well as outsourcing and management of initial design work by design consultancies, consulting chemists, and advanced testing with government research establishments to develop world leading respiratory technology. From 2005 to 2006 (1 year) Mechanical Design Consultant @ International assignment as part of small team designing a rugged Tetra radio handset for the Korean National Police (KNP) force. Responsible for the interface management and analysis of all components and liaison between global sites for the project. From 2004 to 2005 (1 year) Senior Design Consultant @ Engineering design and detail of healthcare, consumer and technical items for a small established product design consultancy. Projects included development PDA's, NBC/CBRN facemask elements and filters for military respirator, vehicle telemetry and ‘Pay as You Drive insurance’ units, handheld electronic calorie meters, digital set top boxes and PVR’s, wireless door chimes, and a human powered flying craft! From 2001 to 2004 (3 years) Product Design Engineer @ Part of a small team designing very high volume GSM mobile telephone handsets for global manufacture. Worldwide tool approval. Conception, design and industrialisation of key major electro mechanical components and mouldings. Global role involving large amounts of time spent travelling and working unsupervised throughout Asia and Europe, problem solving and first off approval for volume production of up to 25 million units per year, from multi-cavity injection mould tools, in mould labelling systems and progressive die sets for metallic components. From 1999 to 2001 (2 years) Innovation Engineer @ From 1998 to 1999 (1 year) Neil Cammish is skilled in: Design for Manufacturing, Medical Devices, R&D, Product Design, Manufacturing, Design Control, Engineering, Product Development, FDA, ISO 13485, Pharmaceutical Industry, Drug Delivery, ISO 14971, Testing, Rapid Prototyping

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In a nutshell

Neil Cammish's Personality Type

Introversion (I), Intuition (N), Thinking (T), Judging (J)

Average Tenure

1 year(s), 11 month(s)

Neil Cammish's Willingness to Change Jobs



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