Client Advisor Dublin 4 Days Jobs In Dublin | WhatJobs

Client Advisor Dublin 4 Days

At Tiffany&Co., joy is central to everything we do, from crafting our exceptional pieces to inspiring clients to express and celebrate the many facets of love. We are looking for thoughtful, curious, and optimistic talents to deliver excellence and contribute to Tiffany&Co.'s continued legacy. Responsibilities

Thoughtful

Deliver unparalleled service and results that uphold standards of excellence and luxury etiquette Demonstrate an entrepreneurial mindset to exceed sales objectives and KPIs Be a trusted Advisor, building client development strategy to drive sales, cross-sales and client loyalty, curating memorable experiences through sales of new creations and servicesEnsure compliance with Tiffany and LVMH procedures, uphold operational excellence standards (inventory, reservation management, transfers, care services excellence, etc.) Contribute to an inclusive and supportive team environment, centered on the belief that People Make the Difference

Curious

Inspire clients through authentic brand storytelling, effectively conveying Tiffany's legacy of craftsmanship, brand commitment and integrity Connect with clients and team members by asking strategic questions and establishing lasting relationships Think and act with intention to elevate, surprise and celebrate clients' special moments and build trust through proactive and relevant services (including personalization and product care services)Display professionalism and exercise agility, adapting behavior and implementing feedback appropriately

Optimistic

Exercise resilience through new challenging assignments and celebrate innovation when adopting new ways of working Exhibit a positive, ambitious and collaborative attitude, instilling an inclusive team culture of Joy

Qualifications

Minimum 3 years of experience in luxury retail environment or client-related experience (e.g., hospitality) Experienced sales and clienteling professional in an omnichannel luxury environment Proven track record in achieving sales results and cultivating relationships with a diverse client base Passion for luxury retail environments; jewelry / watch expertise is a plusCollaborative team player with strong interpersonal and communication skills Thoughtful and service-oriented with knowledge of luxury etiquette Experienced in deploying sales strategies and clienteling initiatives Digitally-savvy and at ease with omnichannel tools Proficiency with Point of Sales (POS) systems, client tracking systems and Microsoft Outlook/emailFlexibility to work non-traditional hours, including days, nights, weekends, and holidays Authorization to work in the United States or in the country where the position is based Preferred

Proficiency in multiple languages A college/university degree Graduate Gemologist degree or previous Gemological Institute of America (GIA) coursework Equal Opportunity Employer Senior Quality Assurance Specialist, Biologics Drug Substance (Remote / Home Based)

Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. Responsibilities

Monitoring daily operations at the Contract Manufacturer, performing batch review and disposition, reviewing and approving product complaints, deviations, Validation protocols, change controls and leading product related investigations CMO Batch file and product testing record review and approval. Associated lot Disposition activityEnsuring compliance of all respective contract manufacturers to both internal Jazz requirements and country specific regulations Collaboration with all contract manufacturers, packagers and testing laboratories to resolve any quality issues Contributing to the successful outcome of all regulatory inspections associated with company business, both internally and at contract manufacturers, as requiredHighlighting any risks associated with maintaining supply of commercial drug products to all markets Conducting vendor audits and vendor site visits as required Assisting in internal audits and regulatory agency inspections Summarizing CMO Annual Product Quality Reviews and supporting regulatory submissionsAssist with the generation of Jazz APQR (Annual Product Quality Review) Maintaining product related Quality Technical Agreements (QTAs) Understanding new regulations and guidelines, as they apply to the company business and implement systems and procedures to incorporate these new regulations as appropriateReview and approve moderate complexity deviations and associated corrective actions Support the generation of new, as well as improvement of, existing department SOPs Support delivery of projects Work with management to resolve project issues and resource constraints within the team Liaise with the internal and external stakeholders to resolve and clarify any point of issueReview and approve less complex validation documents Partner with other departments/groups to problem-solve and address moderately complex issues Collaborate in the continuous improvement of the QA processes, identifying opportunities and leading them up to the implementation Represent QA in cross-functional project teams for moderately difficult projectsParticipate in and facilitate regulatory inspection readiness Coordinates and collaborates with other teams to meet organizational goals and work requirements Receives assignments in the form of objectives and determines how to use resources to meet schedules and goals Follows processes and operational policies in selecting methods and techniques for obtaining solutions; solves moderately complex problems and can identify viable and often innovative optionsUses analytical skills and judgment to recommend the best solution Demonstrates success using compliance knowledge, creativity, and regulatory perspectives to solve problems, especially those associated with major and critical deviations Maintain quality from cell banking through to production and post-release events (e.g., stability, product complaints)Qualifications

Strong knowledge of GMP and Regulatory Compliance as applicable to the Pharmaceutical/ Biotechnology Industry Ability to understand and apply GMP regulations as they relate to manufacturing, QC analytical testing, and facility operations, deep knowledge of Biologics manufacturing Substantial experience working in or directly supporting manufacturing within a biologics drug substance manufacturing siteExperience with contract manufacturing is desirable Significant experience (>5 years) of commercial and/or late state clinical phase GMP manufacturing of biologics Highly organised, with exceptional time management and prioritization Excellent verbal and written communication skills Experience in Drug Product Manufacture in addition to Drug Substance an advantage QP eligibility or progress toward QP certification is highly desirableBachelor’s degree in pharmacy, chemistry, biotechnology, biochemistry, microbiology or a related discipline Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.Buyer/Planner I (Finished Goods)

Buyer/Planner I (Finished Goods) is responsible for ensuring the efficient supply of finished goods by managing purchasing, inventory levels, and vendor performance, directly impacting customer satisfaction and operational efficiency. Responsibilities

Manage purchasing and inventory processes, including placing POs and updating Oracle Monitor demand to maintain inventory targets and optimize stock levels Ensure supply of finished goods across EU warehouses Track and expedite late shipments and respond to supply issues Reduce excess stock and support purchasing/NPI projectsQualifications

Honours Bachelor's degree (Level 8) in a relevant field with at least 1-2 years of relevant experience Excellent written and verbal communication skills Ability to work in a methodical and accurate manner Experience working in an MRP/MPS environment APICS Certification (preferred) Experience using Oracle Manufacturing (preferred)Manager, Finished Goods Supply Planning (Remote Ireland)

Manager, Finished Goods Supply Planning is responsible for setting supply plans in all warehouses in the EMEA region, and ensuring stock availability in each. The position drives material availability actions within Beckman Coulter Diagnostics. Responsibilities

Directly manage up to 8 associates throughout the EMEA region, as well as North America Identify opportunities and implement plans to improve OTD and inventory Work with EMEA L&D to improve freight and material handling costs Lead large, cross-functional groups on improvement initiatives Work with demand planning to create and adjust inventory plans throughout the region Report out group progress against KPIs including employee engagement, OTD, inventory and product availabilityUse the Danaher Business System to drive innovation and change Qualifications

Honours Bachelor's Degree (Level 8) ideally within Supply Chain with a minimum 6 years of experience or Master's degree with 4 years of experience 2 years of experience in direct management of multiple associates Experience leading associates in multiple geographies, representing multiple culturesExperience leading cross-functional groups to attain common improvement goals Excellent written and verbal communication skills Ability to work in a methodical and accurate manner Fluency in a second language (preferred) APICS Certificate (preferred) Ability to travel internation …