Unser Kunde ist ein internationales Unternehmen aus dem Bereich Luxus-Kosmetik & Wellness. Aktuell suchen wir für den Standort Berlin Zentrum nach einem Shop Manager Berlin Zentrum (m/w/d) – Kosmetik & Wellness
Unser Kunde ist ein internationales Unternehmen aus dem Bereich Luxus-Kosmetik & Wellness. Aktuell suchen wir für den Standort Regensburg nach einem Assistent Shop Manager Regensburg (m/w/d) – Kosmetik & Wellness
Unser Kunde ist ein internationales Unternehmen aus dem Bereich Luxus-Kosmetik. Aktuell suchen wir für diverse Standorte im Bundesgebiet nach einem ASSISTENT SHOP MANAGER (m/w) – Kosmetik
Unser Kunde ist ein internationales Unternehmen aus dem Bereich Luxus-Kosmetik Aktuell suchen wir für verschiedene Standorte im Bundesgebiet nach einem Assistent Shop Manager (m/w/d) – Kosmetik
Unser Kunde ist ein internationales Unternehmen aus dem Bereich Luxus-Kosmetik Aktuell suchen wir für den Standort München nach einem Assistent Shop Manager München (m/w/d) – Kosmetik
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.
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.
A multinational pharmaceutical company is looking for a BUD with a minimum total of 10 years of experience in marketing and sales, who will be responsible for driving profitable and sustainable growth for the assigned business unit through the development and implementation of effective short and long term business plans.
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 farmaceutico IL RUOLO Stiamo ricercando un Categoria Protetta- Analista di Laboratorio CQ Junior Con riferimento al Responsabile della Qualità, si occuperà principalmente di eseguire analisi richieste, in accordo alla documentazione ufficiale. Principali attività: • Utilizzare tecniche analitiche strumentali anche di tipo complesso quali GC-FID, GCHS, GC-MSHPLC-UV,ELSD, MS, Analisi termica DSC&TGA; • Utilizzare i principali supporti informatici e le tecniche analitiche strumentali automatizzate; • Compilare in modo adeguato la documentazione relativa alle analisi effettuate; • Rispettare le norme comportamentali e procedurali di laboratorio (Qualità- Sicurezza- Ambiente); • Contribuire allo sviluppo di procedure operative, nonché allo sviluppo e alla validazione di nuove metodologie coerenti con l’attività effettuata ed in linea con le normative di riferimento Luogo di lavoro: Veneto LA PERSONA • Laurea in discipline scientifiche (Chimica, CTF, Farmacia, Chimica Industriale); • Esperienza in laboratorio di analisi o sviluppo analitico in aziende del settore chimico-farmaceutico; • Conoscenza delle linee guide (GMP- GLP) e norme di sicurezza e protezione ambientale; • Gradito background in chimica di sintesi; • Buona conoscenza della lingua inglese; • Attitudine al lavoro di squadra, precisione e ordine, costituiscono titolo preferenziale. Per favore, mandate il vostro CV con una lettera di motivazione al ruolo a: firstname.lastname@example.org Ref: Categoria Protetta- Analista di Laboratorio CQ Junior Le candidature ritenute in linea saranno contattate entro 30 giorni dalla ricezione della candidatura. Grazie fin d’ora tutti coloro che vorranno trasmetterci il loro Cv e, in caso di mancata convocazione, considereremo il profilo professionale per eventuali future esigenze.
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.
Candidate should have 5 + year's experience in content writing in a large organisation (preferably in the pharma sector) or established creative / PR agency ; with proven record of excellent writing in a professional portfolio ; strong Interpersonal and Communications skills .
A multinational pharmaceutical company is looking for a Communication Director with 10 years of experience. He will lead the development, implementation, and drive the public relations (PR) and communication strategy, objectives, plans, tactics, and resources, as well as support all brand-related external communications activities as required in these markets.
Fantastic opportunity to work or a market leading Healthcare organisation based in Watford immediate start, it will be beneficial to have.Required:Minimum 3 to 5 years customer service experienceExperience in ExportPharmaceutical or healthcare backgroundExcellent processing skillsExcellent English verbal and written communication skillsManage complex order process flowExperience in CRM and ERP systemStrong attention to detailCustomer focuseContinue to perform under pressureMulti-task, prioritise, manage time and workload effectivelyWork on own initiative and also as part of a teamFlexible and able to adapt to changes required by the businessBeneficialExperience in wholesaleForeign language: French, Italian, German, Portuguese, Spanish or ArabicParkside Recruitment Ltd is acting as an Employment Agency in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.