My client is a leader within the Defence and Aerospace industry. They are seeking highly capable people to work on cutting edge technologies and inspire our up and coming team members to deliver best in class results.This Senior Systems Engineering role will provide one or more projects with the required Systems Engineering support to ensure the project delivery targets are met and that the technical solution is compliant against all contractual and legal requirements.Key ResponsibilitiesDevelop and manage the contractual functional and non-functional System Requirements.Ensure the technical solution is compliant against the required legislative, Industrial and Military standards.Produce derived requirements for detailed design within the Mechanical, Electrical and Software engineering functionsProduce system test plans and procedures for system verification and qualification.Skills, Qualification and ExperienceEssentialo An HNC/HND in Science or Engineeringo Literate in MS Office toolso A good appreciation of mechanical, electrical and software engineering principals.o Experience in negotiating and agreeing system requirements with customers and stakeholderso Requirements management in IBM DOORso Experience in writing test plans and specificationso Experience in environmental qualification (EMC, Temperature, Shock and Vibration) of systems and sub-systems.o Configuration control of documentation, software and design baselineso Component and sub-system procurement specificationsDesiredo Degree in Science or Engineeringo Chartered Statuso Technical leadership of multi-disciplinary teamso System Modelling Experienceo Knowledge of any of the following Submarine weapon Interface Systems, Naval Data Distribution Systems, Electro-Optical Video Surveillance and Target Tracking systems, Naval Fire Control Systems, Naval Sonar Systems, Naval Combat Management SystemsPersonal AttributesGood communicator both written and face-to-faceA keen interest in the development of new naval and military technologiesAn inquisitive and hands-on approach to solving engineering problemsAssertive and able to prioritise and progress urgent/important tasksEnjoys working in dynamic, team-oriented environmentMust have or be able to achieve SC clearanceParkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.
An exciting opportunity for a Contract Electronics Engineer to contribute to a growing electronics team. My client provide electronics solutions to Maritime Defence industry and are looking for an experienced contract engineer to work alongside the permanent team on high profile programmes with aggressive schedules. The ideal candidate is someone who is familiar with the defence industry and developing military equipment.Key ResponsibilitiesTo interpret customer needs and requirements, to decompose and flow them down into hardware requirements.Conduct electronics design activities and reviews, covering full system, sub-system and individual board design.Ensure that the technical solution meets the customer, legislative and business requirements.To identify and resolve qualification, certification and safety issues.Review and approve project technical documentation, including: Development Plans, Requirements Specifications, Design Documents, Interface Specifications and Acceptance Tests; and the approval of design change requests and concessions.To support risk identification and mitigation activities.Liaising with customers and suppliers as appropriate.Overseeing initial test and integration including formal testingSkills, Qualification and ExperienceBatchelor's degree or equivalent in Electronics or a relevant subject, additionally Chartered status or Professional Registration is desirable.Experience of the whole product lifecycle within a defence environment and/or airborne system qualification.Knowledge of Engineering best practices, methodologies, processes and tools.Knowledge of the EMC standards and design principles.Design experience with Analogue circuits and Technical refresh of legacy systems.Expert user of one or more PMRP and ECAD tools (CADSTAR is desirable, but all others will be considered).Personal AttributesSelf-motivated, adaptable to change, proactive, diligent and excellent inter-personal skills.Eligible for SC clearance as a minimumParkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.
My client is a leader within the Defence and Aerospace industry. They are seeking highly capable people to work on cutting edge technologies and inspire our up and coming team members to deliver best in class results.This Senior Systems Engineering role will provide one or more projects with the required Systems Engineering support to ensure the project delivery targets are met and that the technical solution is compliant against all contractual and legal requirements.Key ResponsibilitiesDevelop and manage the contractual functional and non-functional System Requirements.Ensure the technical solution is compliant against the required legislative, Industrial and Military standards.Produce derived requirements for detailed design within the Mechanical, Electrical and Software engineering functionsProduce system test plans and procedures for system verification and qualification.Skills, Qualification and ExperienceEssentialAn HNC/HND in Science or EngineeringLiterate in MS Office toolsA good appreciation of mechanical, electrical and software engineering principals.Experience in negotiating and agreeing system requirements with customers and stakeholdersRequirements management in IBM DOORsExperience in writing test plans and specificationsExperience in environmental qualification (EMC, Temperature, Shock and Vibration) of systems and sub-systems.Configuration control of documentation, software and design baselinesComponent and sub-system procurement specificationsDesiredDegree in Science or EngineeringChartered StatusTechnical leadership of multi-disciplinary teamsSystem Modelling ExperienceKnowledge of any of the following; Submarine weapon Interface Systems, Naval Data Distribution Systems, Electro-Optical Video Surveillance and Target Tracking systems, Naval Fire Control Systems, Naval Sonar Systems, Naval Combat Management SystemsPersonal AttributesGood communicator both written and face-to-faceA keen interest in the development of new naval and military technologiesAn inquisitive and hands-on approach to solving engineering problemsAssertive and able to prioritise and progress urgent/important tasksEnjoys working in dynamic, team-oriented environmentMust have or be able to achieve SC clearance Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.
My client is a leader within the Defence and Aerospace industry. They are seeking highly capable people to work on cutting edge technologies and inspire our up and coming team members to deliver best in class results.The Analysts are involved throughout the project lifecycle from conceiving new product ideas and capabilities to gaining customer approval of delivered solutions and insertion of capability enhancement to in service solutions.Key ResponsibilitiesDeveloping sonar/acoustics processing algorithms based on the application of established digital signal processing approachesSelecting appropriate algorithmic techniques based upon performance requirements developed with the system design team from the customer specificationDeveloping algorithms with implementation in mind (segmentation/simplification/parallelisation)Documenting algorithm specification and design decisions/implications/discussionsSupporting the implementation, debugging and verification of algorithms in software, including the generation of appropriate test dataPerformance Modelling, Design Trade-offs and Product Development Modelling algorithm performance under a wide range of realistic underwater conditionsModelling sonar/acoustic performance against customer requirements for the inclusion in bid responsesQuantifying the impact of Sonar System Design decisions to the Sonar System performance, hence guiding cost effective approaches to this decision making process.Developing ideas for new approaches to Sonar products to improve their capability individually and collectively embracing new technologies or approachesSupport to Trials Analysing Trials data, assessing against system performance requirementsReporting on Trails Data analysis drawing clear conclusions on both the success of the trials and the sonar system against its performance requirementsCommunication/Reporting Report to project/product development teams on progress of assigned work packagesTo provide in-feed to design reviews and at customer presentationsMentoring junior analysts within the businessSkills, Qualification and ExperienceHold a relevant Bachelor's (higher degree preferred) in Physics, Mathematics;Ideally some experience in one of the following areas, with exposure to the others:Digital Signal Processing Algorithm DefinitionTrials Data AnalysisPerformance Prediction ModellingPerformance Requirement interpretation and analysisExperience in communicating complicated topics clearly and concisely to expert and non-expert audiencesProficient in the use of mathematic/scientific modelling tools e.g. MATLABExperience of being able to set and meet deadlinesHold or be capable of achieving Security Clearance (SC) Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.
My client is a leading Bio-Pharma organisation based in West LondonThey are seeking a Senior Clinical Trial Management Associate on a 12 month contract. The role will involve assisting global trial managers on Phase Ib-III clinical studies, with a strong emphasis on the EMEA region.The successful candidate will be a member of the Global Study team overseen by a Clinical Program Manager. You will work across several studies, including involvement from study start-up through study close-out activities, and will work with the CRO to execute the study to agreed timelines and budget. Essential Duties and Job Functions: Must meet all requirements for Clinical Trial Management Associate position and have demonstrated proficiency in all relevant areas.Provides administrative assistance in site selection, study implementation and ongoing coordination of study sites, either directly or via CROsAssist global trial managers with set-up of central labs and study vendors as required, including liaising with study management CRO to ensure site training and timely initiationPerforms accompanied visits with CRO CRAs to ensure correct study procedures according to company SOPs and protocol procedures, and review of routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as requiredUnder supervision may assist in review of protocols, informed consents, and case report forms, monitoring plans, study plans, abstracts, presentations, manuscripts and clinical study reports. May assist in compilation of investigator brochures under close supervision.Review of trip reports generated by CRO CRAsCommunicates and collaborates with other functional groups including but not limited to Clinical Research, Regulatory Affairs, Development Business Operations (DBO), Clinical Supply Management (CSM) and Pharmacovigilance (PVE) to ensure efficient management of study activitiesAssists with the preparation and organization of international investigator meetingsAssists in preparation of safety, interim and final study reports, including resolving data discrepancies.Performs administrative duties in a timely manner as assignedTravel is required up to 20% Experience, knowledge and skills:Educated to degree level or equivalent within a relevant scientific disciplineMinimum 3 years relevant clinical trial experience in the pharmaceutical or health care industry or equivalent.CRA experience preferred.Excellent verbal, written, interpersonal and presentation skills are required.Must be familiar with routine medical/scientific terminology.Must be familiar with Word, PowerPoint, and Excel.Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.Must be able to participate in departmental or interdepartmental strategic initiative under general supervision.Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.
Antal International è una multinazionale dell’headhunting con più di 130 uffici in 35 paesi. Life science, Chemical and Food è un team specializzato in profili con background scientifico ed ingegneristico in ambito Manufacturing, Produzione, Ingegneria, SCM, Research and Development, Medico, Qualità e tecnico-commerciale nell’ambito Pharma, Chimico Farmaceutico, Biotech, Chimico, Cosmetico, Medicale, Gomma Plastica, Food. LA SOCIETÀ Azienda leader nel settore del Packaging IL RUOLO Stiamo ricercando un Quality Assurance Manager Packaging Il candidato, coordinando le risorse dell’area qualità, si occuperà di assicurare la qualità dell’organizzazione, in ottemperanza alle leggi vigenti in materia e agli standard aziendali Principali attività: • Progettare, implementare e migliorare il Sistema di Gestione della Qualità aziendale, riferendo periodicamente ai vertici aziendali l’andamento del Sistema di Gestione, perché questi possano essere in grado di effettuare un corretto riesame dello stesso; • Promuovere all’interno dell’organizzazione un’idea di qualità intesa come qualità dell’organizzazione e non solo del prodotto, definendo i piani di controllo della qualità; • Applicare le politiche e procedure aziendali per la qualità; • Formare ed informare il personale in merito agli strumenti della qualità che l’organizzazione decide di adottare; • Partecipare e collaborare agli audit per le certificazioni BRC e ISO 9001; • Preparare e aggiornare la documentazione necessaria per descrivere il Sistema di Gestione della Qualità; • Pianificare e condurre le verifiche ispettive interne per sincerarsi che tutte le attività dell’organizzazione avvengano in conformità a quanto descritto nella documentazione di sistema; • Registrare i reclami dei clienti, curando analisi e statistiche ; • Formazione del personale relativamente al sistema di gestione della qualità; • Analizzare i dati e le informazioni derivanti dalle verifiche ispettive e dal controllo statistico di processo per l’impostazione di piani di miglioramento tesi al raggiungimento del livello qualitativo richiesto; • Gestire le azioni correttive derivanti da audit esterno, interno, reclami e non conformità (gestire le contromisure e le azioni correttive definite a fronte di non conformità, resi e reclami, convocando di volta in volta le funzioni coinvolte per aggiornare lo stato di avanzamento) Location: Veneto/ Friuli Venezia Giulia PEOFILO: • Laurea preferibilmente in Materie tecnico scientifiche, Ing chimica, Ctf, Tecnologie alimentari, etc • Esperienza di almeno 5 anni, preferibilmente in contesti produttivi del settore del Packaging o plastico; • Conoscenza ed esperienza nell’uso di strumenti di misura e nell’applicazione dello standard ISO 9001; • Conoscenza dei principali sistemi di total quality; • Fluente conoscenza della lingua inglese; • Problem solving e ottime doti relazionali Si prega di inviare CV e lettera di motivazione al ruolo a email@example.com Riferimento:– QUALITY ASSURANCE MANAGER PACKAGING
My client is a leading research-based biopharmaceutical organisation. They are seeking and experienced Business Systems Analyst to join the team on a 6 month basis.Business Analyst with IT GxP process and Business Process implementation experience.Seasoned Senior Business Analyst with strong core skills, including communication, leadership, taking the initiative, and driving for results with little support from other BA team members.RoleImplement advanced strategies for gathering, reviewing and analyzing requirementsPrioritize requirements and create conceptual prototypes and mock-upsMaster strategic business process modeling, trace ability and quality management techniquesApply best practices for effective communication and problem-solvingCreates clear and concise documentationResponsibilities:Partner with cross-functional stakeholders (i.e.: IT Security team, Project Sponsor, Validation/Qualification team and Business counterparts, etc.) to elicit, analyze, and translate information to create Business Requirement , User Requirements, and/or Technical RequirementsAct as a liaison between technical teams, senior management, and the business community, including managing communications between business stakeholders and technical teamsTraceability Matrix creation and managementLead effort to obtain approvals for all types of RequirementsManage user change requests and change processWork with IT Security team, Project Sponsor, Validation/Qualification team and Business counterparts, etc. to gather and analyze information to develop new and update existing Process Flows and accompanying documentation (including swim-lanes diagrams and As-is & To-be documentation, etc.)Design comprehensive test plans to test the quality of software and business processesWork with IT Security team, Business counterparts, etc. to gather information to create User Acceptance Test Strategy documentsCoordinate and manage user acceptance testing by providing test schedules, planning, test data, detailed test scripts and document test resultsLead effort to obtain approvals for UAT Testing Summary, including the creation of the summary itself.Work with Technical and Training Team to develop Training Plan, Materials, Training execution and Manage Training Plan approvals.Work with Technical and Business team to develop Support Plan and Manage approvals.Work with Technical and Business team to develop end-user communication. Minimum Requirements:7 years analyst experience preferred.Ability to elicit business requirements and translate into technical solution design documentsWorking knowledge of business processes, system development and process improvements.Proficient in gathering business requirements using UML, process flows and uses cases.Expertise in modeling and mapping as-is and to-be business processes.Experience with complete software development life cycle.Understanding of technology capabilities and limitations.Experience with and strong understanding of various technologies and platforms, including end-point devices (i.e. mobile devices, laptops, tablets, servers, etc.)Experience designing and reviewing test cases.Experience with QA (GxP) process methodologyKnowledge of SharePoint or similar collaboration portalSelf-starter with strong problem solving skillsExcellent verbal and written communication skills..National or international travel is not expected..Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.
For our client, a large multinational company, we are currently looking for a Senior Data Protection Manager (m/f/d) - Temporary role for 12 months for their headquarter in Nuremberg.
My client is a leading research-based bio-pharmaceutical organisation they have a great to opportunity for an Associate Director - Medical Affairs.This is a 15n month contractHead of Medical Affairs Operations - Associate Director Skills for Position: o Demonstrated ability to manage several medical projects within designated program budgets and timelines is required. o Demonstrated excellence in complex project management and effectively managing multiple projects/priorities is required. o Support team members and empower them to complete deliverables efficiently and effectively. o Ability to initiate and lead departmental or interdepartmental strategic initiatives. o Proven ability to effectively communicate scientific, medical, and organizational concepts to internal and external customers. o Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of complex problems o Organize and manage Medical project team meetings, ensuring timely, efficient, and action-oriented operations. o Manage external collaboration project and all associated interactions (e.g. meetings, communications etc.) with the partner agencies and ensure agencies deliver projects in accordance to agreed timelines, scope, budget and compliance o Direct project communications to relevant team members and ensures that all stakeholders (internally and externally) are fully informed and knowledgeable of project activities and their status. o Implement best-in-class project management processes and tools/templates such as project schedules, Gantt charts, action/decision logs, risk registers, SharePoint site etc. o Provide inputs on behalf of the LT for the LE process. Manage cross-functional initiatives/projects to enable advancement of sciences and improve alignment and efficiency. o Prepare agenda, minutes, and action items for Leadership Team meetings Knowledge: o Excellent verbal, written, interpersonal skills, and ability to work with multifunctional teams o Must be able to effectively communicate progress toward milestones, opportunities, and risks to all stakeholders. o Must exhibit high emotional intelligence, with demonstrated ability to successfully negotiate through challenging situations and difficult conversations. o Possess a strong ability to build trust, along with demonstrated ability to drive, lead and influence colleagues across the organization to achieve team, department and corporate goals. o Must be a team player, focusing on shared goals, being flexible and applying skills where required, respecting others, listening to others' views and value others' contribution, sharing information and good ideas across organizations and celebrating/recognizing accomplishments. o Must have strong leadership skills and ability to effectively develop teams o Must be comfortable and efficient in a fast-paced, dynamic and growing environment. o ability to prioritize and execute tasks both as an individual contributor and in a team-based setting o History of motivating others to deliver to important milestones while maintaining a positive, transparent and collaborative team environment o Capable of assessing and updating detailed project timelines in meetings to guide and align study team members o Ability to evaluate meeting minutes and materials for required updates to project timelines o Ability to work on complex and multiple projects while exercising critical thinking with minimal supervision o Solid attention to detail and excellent organization skills o Ability to establish priorities, operate with a sense of urgency and collaborate (interpersonal, relationship management) with the study team, cross functional team members o Demonstrates problem solving skills, demonstrates leadership skills, self-motivated and adaptable to a dynamic environment o Computer skills including proficiency in the use of Microsoft Project, Word, Excel, PowerPoint, and organization tools o Proficient with SharePoint with filing systems is desirable o Ability to deal with time demands, incomplete information or unexpected events o Must display strong analytical and problem solving skills o Occasional travel to other company locations as requested. Requirements: o At minimum, a bachelor's degree in nursing, science or health related field required, higher degree, MSc, PhD preferred o Medical Affairs Experience o Project manager/Management experience Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.
Our reputed client based in Riyadh, Saudi Arabia is looking to hire a FP&A Manager - Temporary Appointment in Financial Technology industry.