Keeran Roberts Email & Phone Number

Worthing, England, United Kingdom

I am the regulatory responsible person for all key aspects of our product’s. My responsibilities are but not limited to:- All mandatory regulatory approvals- Safety technical report reviewer - EMC technical report reviewer- EMC lab manager and project lab scheduler.- Working with Global regulatory bodies on regulatory requirements for our products ( Medical, Aerospace, Nuclear, Military).- Working with external safety test labs on our Global Approval testing.… Show more I am the regulatory responsible person for all key aspects of our product’s. My responsibilities are but not limited to:- All mandatory regulatory approvals- Safety technical report reviewer - EMC technical report reviewer- EMC lab manager and project lab scheduler.- Working with Global regulatory bodies on regulatory requirements for our products ( Medical, Aerospace, Nuclear, Military).- Working with external safety test labs on our Global Approval testing. - EMC test engineer and report writer. - EU business projects lead for all data cabinet technical files and regulatory testing Working with the following test standards:- IEC 61010-1- IEC 61010-2-201- IEC 61326-1 Show less

Weaterham

IRCA Accredited Internal Auditor covering ISO 9001

Kent, England, United Kingdom

I am the key person looking after all legal and voluntary regulatory approvals and requirements for the Aqualisa Group of companies (Aqualisa, Gainsborough and Elisa Bathrooms).Responsibilities within the business but not limited to:• Key company signatury for all WRAS, EU Water approvals and TMV2 approvals. . Providing key ESG requirements for all our products. This covers water saving ECO modes through to recycling of packaging etc. • Ensuring Aqualisa Group of… Show more I am the key person looking after all legal and voluntary regulatory approvals and requirements for the Aqualisa Group of companies (Aqualisa, Gainsborough and Elisa Bathrooms).Responsibilities within the business but not limited to:• Key company signatury for all WRAS, EU Water approvals and TMV2 approvals. . Providing key ESG requirements for all our products. This covers water saving ECO modes through to recycling of packaging etc. • Ensuring Aqualisa Group of companies is meeting its legal regulatory obligations through various legal regulatory testing and approvals.• Responsible for all regulatory approvals on new and existing products.• Responsible for all but not limited to Global Safety, EMC, RED/RER, WRAS, TMV2, European Mandatory Water Regulations, and upcoming TMV3 approvals.• Responsible for the technical file generations and ensuring all test reports meet the latest test standards. • Working with third party test houses on all testing required for the business.• Project management of all U.K. and Global regulatory projects for the business. Show less

Dorking, Surrey, United Kingdom

Head of the corporate quality and compliance FMCG activities for the Gift Universe group of companies (MenKind, RED5, The Source Wholesale, Gadget Grotto and Querkity).Responsibilities:• ensure all imported toy, clothing and food products comply to product legislation for UK and worldwide requirements.• management of the quality and compliance requirements for each order throughout the critical path.• working close with BDM and buying teams throughout the business on… Show more Head of the corporate quality and compliance FMCG activities for the Gift Universe group of companies (MenKind, RED5, The Source Wholesale, Gadget Grotto and Querkity).Responsibilities:• ensure all imported toy, clothing and food products comply to product legislation for UK and worldwide requirements.• management of the quality and compliance requirements for each order throughout the critical path.• working close with BDM and buying teams throughout the business on product quality assessments and product risk assessments. • working close with design teams on legal copyright artworks. • creating and maintaining existing databases including the ISO 9001 QMS system. • working close with UK and International test houses on product compliance assessments.• management of the quality and compliance department both in the UK and the Far East.•managing the quality and compliance budgets.• key person in dealing with Trading Standards, lawyers and HM courts and tribunal services queries on product failures. Show less

Camberley, Surrey, United Kingdom

- Responsible for keeping regulatory trackers up to date on all hardware projects.- Responsible for all pest hardware projects within the marketing and innovation division. - Responsible for all air purification projects from a regulatory aspect.- Responsible for the Lumnia Slim project. - Key regulatory contact within the Rentokil Group for all existing and upcoming hygiene projects. - Actively coordinating all regulatory testing (EMC, Safety, RED, IECEE CB Scheme, Global… Show more - Responsible for keeping regulatory trackers up to date on all hardware projects.- Responsible for all pest hardware projects within the marketing and innovation division. - Responsible for all air purification projects from a regulatory aspect.- Responsible for the Lumnia Slim project. - Key regulatory contact within the Rentokil Group for all existing and upcoming hygiene projects. - Actively coordinating all regulatory testing (EMC, Safety, RED, IECEE CB Scheme, Global Approvals, RoHS and REACH) with test houses in the UK and abroad. - key contact within the Rentokil group on upcoming regulations which could affect their current product compliance strategies.- Global regulatory contact within Rentokil Initial covering any relevant country specific requirements.- Responsible for creating Rentokil Initials product technical files for CE, NRTL etc declarations. - Responsible for the generation of Risk Assessment documents on the products / projects I am responsible for. - Responsible for all of Rentokil Initials 110/240Vac product plug and cable requirements for UK and International markets. Show less

Fareham

• Working with medical device manufacturers in ensuring they meet the legal regulatory requirements to sell their products both Nationally and Internationally. • Working close with the MHRA in relation to pulled products from the market.• Working with manufacturers in ensuring their products meet the requirements of IEC 60601-1 (safety), IEC 60601-1-2 4th Edition (EMC), IEC 62304 (Software), IEC 61010-1 (Laboratory and IVD Devices).• Reviewing technical files to ensure… Show more • Working with medical device manufacturers in ensuring they meet the legal regulatory requirements to sell their products both Nationally and Internationally. • Working close with the MHRA in relation to pulled products from the market.• Working with manufacturers in ensuring their products meet the requirements of IEC 60601-1 (safety), IEC 60601-1-2 4th Edition (EMC), IEC 62304 (Software), IEC 61010-1 (Laboratory and IVD Devices).• Reviewing technical files to ensure they are up to date and meet the requirements of the Medical Device Directive.• Planning of regulatory testing with test engineers, project coordinators and medical device auditors.• Identify potential risks through the review of technical files and potential pit falls that clients could face with new markets they are looking to sell into.• Working on projects in accordance with the MDSAP requirements.• Providing consultancy services on testing, market requirements, certification requirements for Global market access.• Reporting to company directors on sales figures, cross function services and project management timeframes.• Working on active and non-active medical devices. • Increasing revenue through department service cross selling.• Responsible for all B2B field related activities.• Responsible for ensuring and maintaining medical auditors diaries are booked with work 1 year in advance.• Providing small to large companies with their legal Regulatory requirements for Global Market Access. • Ensuring engineering team-members schedules are booked with on-going testing and approval projects.• Generating technical quotes, bids and high-level proposals.• Ensuring medical clients are meeting the regulatory requirements for CE marking under the EN ISO 13485:2016 QMS regulations.Medical Auditing: ISO 13485Bio compatibility: ISO 10993 EN, IEC, UL, CSA 60601 and the relevant part 2.ISTA 2 and 3A - Medical package testing Show less

Watford, United Kingdom

My career responsibilitiesI am responsible for bringing in new business through face to face meetings, prospecting business through LinkedIn, competitor online directories, networking at seminars and training events. My primary role is to ensure sales targets are met on a monthly basis as well ensuring clients are meeting their regulatory requirements.- Business Development and strategy- Pitching regulatory affair requirements to clients at various levels including CEO/VP… Show more My career responsibilitiesI am responsible for bringing in new business through face to face meetings, prospecting business through LinkedIn, competitor online directories, networking at seminars and training events. My primary role is to ensure sales targets are met on a monthly basis as well ensuring clients are meeting their regulatory requirements.- Business Development and strategy- Pitching regulatory affair requirements to clients at various levels including CEO/VP and directors- Reviewing medical device technical files in accordance with the MDD and FDA requirements. - Providing consultancy services to active and none active medical device manufacturers on regulatory requirements for Global Market Access. - Pitching to client at various level including CEO/VP and directors- Securing book and bill opportunities to exceed operational revenue budgets.- Market analysis to identify new industries to sell within ahead of competition50% new account and 50% existing account management- Concentrating on the following service standards:Electrical safety:EN/IEC 60950 seriesEN/IEC 60335 seriesEN/IEC 61010 seriesEN/IEC 60601 seriesEN/IEC 60065EN 60204Machinery Safety DirectivePUWERRoHSErPApprovals:IECEE CB schemeMET (NRTL) schemeGlobal approvals - RCM mark etc. Show less

Cleeve Road, Leatherhead, Surrey

Responsible for bringing in new business Targeting the MCS database and prospecting potential client (cold calling)Increasing sales by selling additional services to current client baseAdvising resulatory requirements for Global Market Access

Leatherhead Uk.

I am the Senior Account Manager for the Information, Communication and Technology Sector at Intertek Leatherhead, Surrey UK. I work close with all ICT manufacturers, developers, importers and exporters who look to gain market entry. Role:Business Development and strategyPitching regulatory affair requirements to IT and Telecom clients at various levels including CEO/VP and directorsSecuring book and bill opportunities to exceed operational revenue budgets.Market… Show more I am the Senior Account Manager for the Information, Communication and Technology Sector at Intertek Leatherhead, Surrey UK. I work close with all ICT manufacturers, developers, importers and exporters who look to gain market entry. Role:Business Development and strategyPitching regulatory affair requirements to IT and Telecom clients at various levels including CEO/VP and directorsSecuring book and bill opportunities to exceed operational revenue budgets.Market analysis to identify new industries to sell within ahead of competition50% new account and 50% existing account managementConcentrating on the following service standards:Electrical safety:EN/IEC 60950-1 seriesGR-63-COREGR-1089-COREApprovals:IECEE CB schemecETLus (NRTL) schemeGlobal approvals - CCC Mark etc.Territories: EMEA, Australia, South Africa, Benelux Regions. Show less

Leatherhead

Internal sales for the Home Appliance, Audio Visual and Lighting industries. Role:Exceeding set targetsB2B regulatory affair requirements over the phone with some internal face to face client interactionTargeting competitor clients through various mediums such as LinkedInShow casing Interteks services at National and International trade shows.Securing book and bill opportunities to exceed operational revenue budgetsConcentrating on the following… Show more Internal sales for the Home Appliance, Audio Visual and Lighting industries. Role:Exceeding set targetsB2B regulatory affair requirements over the phone with some internal face to face client interactionTargeting competitor clients through various mediums such as LinkedInShow casing Interteks services at National and International trade shows.Securing book and bill opportunities to exceed operational revenue budgetsConcentrating on the following standards:EN/IEC 60335 seriesEN/IEC 60065 seriesEN/IEC 60598 seriesEnergy StarErP Approvals:IECEE CB schemecETLus (NRTL) schemeGlobal Approvals e.g. RCM, CCC mark etc.Regions: UK and Ireland, Benelux Regions Show less

Crawley, West Sussex, United Kingdom

Police constable. Worked on the front line of policing for Crawley West Sussex covering anti social disorder, burglary, theft etc. I was made redundant due to government cut backs.

London, United Kingdom

British Army Soldier - Various rolesGrenadier Guardsman (Mortar and HMG Platoon)London Guards Regiment - HQ Household Division Battle Group (Signals and Technical Specialist Operator)

O Levels, English, Science, Commerce, Agriculture, Maths., O Levels

Activities and Societies: Second team field hockey, second team swimming, brass orchastra, percussion band, School pupils council.

Diploma In Professional Photography, Professional Photography, Diploma

Activities and Societies: Camera & lenses Shutters, Aperture, ISO & Their Relationship Exposure & Metering The Film & Digital Process.

Diploma Level 5, Leadership And Management

Achieved Level 5 Diploma in Leadership and Management.