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Experience Level
Experience
Qualifications
Proven experience in external communications, media relations, or public relations. Exceptional written and verbal communication skills. Strong understanding of communication strategies and tools. Ability to work collaboratively with cross-functional teams. Experience in crisis communications is a plus.
About the job
We are seeking a dynamic and experienced Senior External Communications Manager to join our team at Primark in Dublin. The ideal candidate will play a crucial role in shaping our external communications strategy, building brand visibility, and fostering relationships with key stakeholders.
This position requires a strong communicator with a proven track record in managing external communications, media relations, and public relations campaigns. You will lead initiatives that enhance Primark’s reputation and visibility across various platforms.
About Primark
Primark is a leading fashion retailer known for offering stylish and affordable clothing. With a strong commitment to sustainability and ethical practices, we aim to bring the latest fashion trends to our customers while ensuring a positive impact on the environment.
Cytokinetics stands at the forefront of cardiovascular biopharmaceutical innovation, dedicated to the discovery, development, and commercialization of pioneering muscle activators and inhibitors aimed at treating debilitating conditions linked to compromised cardiac muscle performance. With a robust expertise in muscle biology and performance mechanics, our …
Cytokinetics is a pioneering biopharmaceutical company specializing in innovative cardiovascular treatments. Our focus is on the discovery, development, and commercialization of first-in-class muscle activators and next-in-class muscle inhibitors aimed at addressing severe diseases that compromise cardiac muscle performance. As a frontrunner in muscle biology, we are dedicated to creating small molecule drugs designed to enhance myocardial function and contractility.Job PurposeIn the role of Manager, External Manufacturing and Supply Operations, you will oversee the comprehensive technical and operational aspects of external manufacturing and supply activities within a network of Contract Manufacturing Organizations (CMOs). This pivotal position within Manufacturing and External Supply Operations demands a solid technical foundation and the capacity to handle multiple priorities in a dynamic and fast-paced environment.This position emphasizes the review and approval of batch records, process oversight, and informed technical decision-making, ensuring compliance with cGMP standards and alignment with global supply needs.Your role will involve extensive collaboration with Quality Assurance, Technical Operations, Regulatory Affairs, and Supply Chain to ensure a robust, compliant, and dependable supply chain for both clinical and commercial products. You will report directly to the Director of External Supply Operations.
Join AbbVie as an Associate Director of Supply Chain Brand, where you will play a pivotal role in driving our supply chain strategies to meet the dynamic demands of our business. You will collaborate with cross-functional teams to ensure the seamless flow of products and services while maintaining the highest standards of quality and efficiency. Your leadership will be crucial in optimizing our supply chain operations and achieving our business objectives.
Anduril Industries is a leading defense technology firm dedicated to revolutionizing military capabilities for the U.S. and allied forces through state-of-the-art technology. By integrating the innovative approaches and business models of the 21st century's most forward-thinking companies into the defense sector, Anduril is transforming the way military systems are conceived, constructed, and marketed. Our suite of systems operates on Lattice OS, an AI-enhanced platform that converts vast data streams into a real-time, 3D command and control interface. As global strategic competition intensifies, Anduril is committed to delivering cutting-edge autonomy, artificial intelligence, computer vision, sensor fusion, and networking technologies to defense applications in record time.About The Team:The Voyager team at Anduril Industries is a specialized engineering and design group with extensive expertise in creating innovative computing and communications solutions tailored for the network edge. This team excels at merging enterprise networking capabilities from top global IT providers with custom hardware and software platforms that meet rigorous environmental specifications.We are currently in search of an Operations & Supply Chain Associate to become a vital part of our Production team in Dublin. This position demands a comprehensive knowledge of logistics, the ability to collaborate across various teams, meticulous attention to detail, adaptability in ambiguous situations, and a strong desire to rapidly acquire new knowledge.
At Olema Oncology, we are committed to pioneering advanced treatments for breast cancer and other malignancies. Our flagship program, palazestrant (OP-1250), is an innovative complete estrogen receptor antagonist (CERAN) currently under development for metastatic breast cancer, showcasing significant potential both as a standalone treatment and in combination therapies for ER+/HER2- metastatic breast cancer. Additionally, we are excited about our next product candidate, OP-3136, a leading KAT6 inhibitor poised to set new standards in treatment efficacy.Our culture thrives on collaboration, where we empower, inspire, and challenge each other to achieve remarkable breakthroughs. At Olema, placing our people first translates into groundbreaking advancements in medicine. Join us in our mission to create a profound impact for our patients and elevate your career to new heights.For more insights, please explore our latest corporate presentations here.About the Role >>> Senior Director, Commercial Manufacturing & OperationsAs the Senior Director of Commercial Manufacturing & Operations, reporting directly to the SVP of CMC and Supply Chain, you will leverage your extensive management experience and proven track record in leading complex projects related to late-stage manufacturing of small molecule drug substances and products. You will oversee the technical transfer process (including validation activities), manage manufacturing operations, and ensure the integrity of documentation and quality standards across drug substances and products.This position is based in our Dublin, Ireland office, with an expected travel requirement of 20%.Your primary responsibilities will include:Providing technical and operational leadership in drug substance (DS) and drug product (DP) commercial manufacturing, along with CMO management.Creating and refining business processes and systems to enhance DS and DP commercial activities, collaborating globally to implement these within Olema’s CDMO network.Developing performance metrics and spearheading continuous improvement initiatives.Fostering site leadership with a keen awareness of employee engagement, ensuring alignment with Olema’s corporate strategy.Overseeing the review and approval of documentation (MBRs, specifications, etc.) to maintain compliance and quality standards.
We are seeking a dynamic and experienced Senior External Communications Manager to join our team at Primark in Dublin. The ideal candidate will play a crucial role in shaping our external communications strategy, building brand visibility, and fostering relationships with key stakeholders.This position requires a strong communicator with a proven track record in managing external communications, media relations, and public relations campaigns. You will lead initiatives that enhance Primark’s reputation and visibility across various platforms.
Join our dynamic team at Mufg Investor Services as an Associate Director of Finance. In this pivotal role, you will oversee financial operations, ensuring compliance with regulations and driving strategic financial planning. Your expertise will contribute to our growth and success in the investment services sector.
Join AbbVie as the Associate Director of Business Excellence and play a pivotal role in driving organizational improvements and operational excellence. In this leadership position, you will collaborate with cross-functional teams to implement best practices, streamline processes, and enhance overall business performance.
Role overview The Associate Director of Development Infrastructure at AECOM in Dublin takes on a senior leadership position, overseeing a variety of development and infrastructure projects. This role carries responsibility from the initial planning stages through to final delivery. The Associate Director supervises project teams, tracks progress, and ensures that all work meets quality and compliance standards at every step. Key responsibilities Lead and manage teams focused on development infrastructure projects Oversee the execution of development strategies to achieve project objectives Maintain alignment with quality standards and regulatory requirements throughout project lifecycles About AECOM in Dublin AECOM provides infrastructure consulting and project management services worldwide. The Dublin office supports a diverse portfolio of complex development projects, contributing expertise to significant initiatives across the region.
Join Interpath, a dynamic and rapidly expanding international advisory firm, recognized for our deep expertise in a diverse array of specialisms, including deals, advisory, and restructuring capabilities.We are committed to delivering measurable results for global enterprises, their investors, and stakeholders during challenging times when pivotal decisions must be made. Our independence and agility, paired with a strong ethical foundation, differentiate us in the marketplace.Our diverse teams combine specialized technical knowledge with extensive sector experience across various service lines. Since our inception in 2021, Interpath has seen significant growth, establishing a presence in the UK, Ireland, France, Switzerland, Germany, Austria, Spain, BVI, Cayman Islands, Bermuda, Barbados, and Hong Kong. We aspire to become one of the world's leading advisory firms by 2030, solidifying our global reach.This role presents a unique opportunity to engage in prominent mid-market transactions across various sectors. You will provide guidance to business owners, corporate leaders, and private equity investors, gaining hands-on experience in intricate deal negotiations and financial analyses, ultimately influencing both client success and Interpath's expansion.As an Associate Director within our Corporate Finance (M&A) Advisory team, you will be instrumental in executing transactions, managing client relationships, and mentoring junior team members. Your proficiency in the M&A sector will be crucial as you navigate clients through complex deals while aiding in the growth of our business.Key Responsibilities:Oversee the execution of M&A transactions, ensuring prompt delivery and client satisfaction.Perform comprehensive financial analyses and create detailed models to guide transaction decisions.Develop high-caliber presentations and marketing materials to effectively convey transaction strategies.Act as the primary liaison for clients throughout the transaction lifecycle, cultivating relationships for repeat business.Lead business development initiatives, identifying potential clients and opportunities within targeted sectors.Mentor and support junior team members, fostering a culture of continuous learning and professional growth.Keep abreast of industry trends and market developments to provide informed guidance to clients.
Join Interpath Advisory, a dynamic and rapidly expanding international advisory firm renowned for its expertise in a wide array of specializations including deals, advisory, and restructuring. Our mission is to deliver effective solutions for global businesses, their investors, and stakeholders during complex challenges and critical decision-making processes. With an agile, independent, and conflict-free approach, our commitment to integrity and excellence truly differentiates us.Since our establishment in 2021, we have swiftly grown and now operate in countries such as the UK, Ireland, France, Germany, Austria, Spain, Switzerland, BVI, Cayman Islands, Bermuda, Barbados, and Hong Kong. We aspire to be among the world's leading advisory firms with a significant global presence by 2030.We are currently seeking a Dispute Advisory Associate Director to enhance our Forensics team in Dublin. This is a unique opportunity to play a pivotal role in creating a top-tier Forensic & Investigations Services team while engaging in high-impact projects from the outset.
At Olema Oncology, we are committed to revolutionizing the treatment landscape for breast cancer and other conditions. Our flagship program, palazestrant (OP-1250), represents a groundbreaking complete estrogen receptor antagonist (CERAN) currently under development for metastatic breast cancer, showing exceptional promise as both a standalone therapy and in combination for ER+/HER2- metastatic breast cancer. Additionally, our next candidate, OP-3136, is a leading KAT6 inhibitor poised to set new standards in treatment efficacy.We foster an environment of innovation, encouragement, and mutual challenge, knowing that prioritizing our people leads to unparalleled outcomes. If you are eager to be a part of a transformative journey, let's create meaningful change together for our patients, your career, and the future.To explore our latest corporate presentations, click here.Position: Associate Director of Formulation DevelopmentIn your role as Associate Director of Formulation Development, you will report to the Senior Director of Drug Product. You will spearhead pre-formulation and formulation development, tech transfer, scale-up, and manufacturing initiatives at Olema’s Contract Manufacturing Organizations (CMOs) or Contract Development and Manufacturing Organizations (CDMO). This pivotal role entails providing scientific insights into solid oral dosage formulation development, managing early to late-stage process development, overseeing GMP drug product manufacture at contract facilities, authoring global regulatory submissions (INDs, IMPDs, NDAs, etc.), as well as ensuring the validation of packaging, shipping, and transportation in preparation for commercial launch. You will work collaboratively with cross-functional teams and other CMC functions in a dynamic, high-growth setting to advance Olema’s small molecules from discovery to commercialization.This position is based in our Dublin, Ireland office and will require 25-30% travel.Your responsibilities will include:Leading preclinical and early clinical phase formulation development efforts at CMOs and overseeing tech transfer to GMP vendors for clinical drug product manufacture and scale-up.Designing and supervising formulation development activities, ensuring alignment with regulatory standards and timelines.
Join our dynamic team as the Senior Associate Director of Financial Reporting at Mufg Investor Services. In this pivotal role, you will oversee financial reporting processes and ensure compliance with regulatory standards. Your expertise will guide the development and implementation of accounting policies while collaborating with various stakeholders to enhance reporting efficiency.
About the Role Mufg Investor Services is hiring a Junior Associate Director for Regulatory Compliance in Dublin. This role centers on supporting the firm's commitment to regulatory standards and effective compliance practices. Main Responsibilities Monitor ongoing compliance activities across the business Conduct audits to assess adherence to regulatory requirements Work with teams from different departments to address compliance matters Offer guidance on interpreting and applying relevant regulations Contribute to the development of compliance strategies in line with industry standards Collaboration This position involves frequent collaboration with colleagues across multiple functions, supporting a unified approach to compliance throughout the organization.
AbbVie Inc. seeks a Global Supply Planner based in Dublin. This position manages the flow of products across multiple countries, ensuring that supply aligns with business needs through detailed planning and coordination. Key responsibilities Create supply plans that support company objectives and meet global demand. Maintain the right balance between inventory and production capacity to keep products available when needed. Use demand forecasts to anticipate requirements and reduce the risk of supply interruptions. This role focuses on supporting international operations by keeping products moving efficiently and reliably to markets worldwide.
The Senior Associate Director of Business Operations Controls will lead the Controls team at Mufg Investor Services in Dublin. This position focuses on maintaining compliance with regulatory standards and improving operational efficiency throughout the organization. Role overview This leadership role involves working closely with teams across different functions to put effective practices in place and support ongoing improvement efforts. The Senior Associate Director will set direction for the Controls team, ensuring strategies align with business objectives and regulatory expectations. Key responsibilities Oversee compliance with regulatory requirements within business operations Identify and implement process improvements to enhance efficiency Collaborate with other departments to share best practices and drive initiatives Promote a culture focused on risk awareness and accountability Develop and execute strategies that support organizational goals What we look for Experience leading teams in a business operations or controls environment Strong understanding of regulatory compliance Ability to manage complex challenges and drive continuous improvement Proactive approach to problem-solving and risk management
Mufg Investor Services is seeking a Senior Associate Director of Business Operations Controls in Dublin. This leadership position centers on building and refining controls that support compliance and strengthen operational efficiency across the organization. Role overview The Senior Associate Director will guide the creation and rollout of business operations controls. The role involves working closely with teams from different functions to assess risk, evaluate current processes, and identify areas for improvement. Maintaining regulatory compliance is a key responsibility, as is ensuring that operations consistently align with internal standards. Key responsibilities Lead the design and implementation of controls for business operations Partner with cross-functional teams to assess risks and improve processes Support ongoing regulatory compliance efforts Contribute to the development of operational strategies that uphold process integrity Requirements Demonstrated expertise in business operations controls Experience collaborating with multiple teams on risk and compliance matters Strong understanding of regulatory requirements and process improvement
As a Junior Associate Director in Fund Accounting for Private Debt, you will report directly to the Associate Director of Client Operations within Fund Administration. Your key responsibilities will encompass:Delivering comprehensive fund accounting and administration services tailored to Private Debt clients, including the preparation and review of Net Asset Value (NAV), custody servicing, investor record keeping, and reporting.Overseeing Fund Accountants to ensure efficient service delivery and providing training on all aspects of the NAV process.Collaborating with banks, auditors, brokers, and custodians to facilitate seamless service to clients and to conclude the NAV process effectively.Reviewing fee schedules, including the calculation of management and performance fees, ensuring adherence to relevant fund documentation.Training and mentoring junior staff to enhance their skills and knowledge.Authorizing the payment of fund expenses through the relevant banking systems while ensuring compliance with established controls.Assisting in the preparation and review of audited financial statements and annual audits.Ensuring compliance with reporting standards for regulatory authorities.Generating innovative ideas aimed at optimizing the NAV process, implementing technological advancements, and enhancing client reporting.
About Articul8 AIArticul8 is at the forefront of innovation, developing enterprise-grade Generative AI solutions designed to help organizations worldwide extract unprecedented value from their data. Our platform is a trusted asset for some of the most forward-thinking companies globally, as we collaborate closely with our clients to tailor, deploy, and expand AI solutions that yield tangible outcomes.As a dynamic startup, we prioritize agility and focus. Each team member enjoys a sense of ownership, and your contributions will have a direct influence on our platform and our clients' achievements. If you excel in a setting where innovation is a daily occurrence and your impact is evident, Articul8 is the perfect place to advance your career.Role OverviewAs the Manufacturing & Industrial Solutions Architect, you will play a pivotal role in collaborating with leading manufacturing enterprises to design, implement, and enhance scalable, flexible, and resilient cloud architectures. This senior technical position demands a blend of profound manufacturing and industrial knowledge, cloud architecture expertise, and a commitment to customer success to create measurable business value. Your responsibilities will also include influencing the product roadmap by integrating customer feedback and market insights into our solution strategies and product development efforts within complex enterprise landscapes.Key ResponsibilitiesDesign and deploy scalable architectures tailored for manufacturing applications, including industrial operations such as SCADA/HMI, EDA, IoT, Machine Learning, AI, and advanced analytics.Facilitate technical workshops, prototype innovative solutions, and supervise platform deployment and optimization efforts.Engage collaboratively with product and engineering teams to incorporate customer insights into the evolving product roadmap.Provide strategic advice to customers regarding Articul8 product adoption, with a focus on unique capabilities, security, cost efficiency, and operational effectiveness.Architect and optimize Kubernetes-based and containerized infrastructures leveraging cloud platforms (AWS, Azure, GCP, or on-premises) to ensure excellence.Create reusable solution templates and document industry best practices.Collaborate with sales and business development teams to promote cloud adoption and ensure alignment with industry trends.
Join Olema Oncology, a pioneering company committed to developing innovative treatments for breast cancer and beyond. Our flagship program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently under development for metastatic breast cancer, showcasing tremendous potential as both a monotherapy and in combination therapies for ER+/HER2- metastatic breast cancer. Additionally, our follow-on candidate, OP-3136, is a potent KAT6 inhibitor poised to lead the market.At Olema, we drive scientific breakthroughs through our unwavering support, motivation, and challenge of one another. We believe that by prioritizing our people, we can achieve unparalleled results. If you are ready to be part of an unstoppable force and make a meaningful impact for our patients, your career, and beyond, we invite you to join us.Discover more about us in our latest corporate deck and presentations.About the Role >>> Associate Director, GMP Quality – Qualified PersonAs the Qualified Person (QP), reporting to the Senior Director of Quality Assurance based in San Francisco, California, you will be instrumental in ensuring that our Clinical and Commercial products are manufactured, tested, and released in accordance with the regulatory requirements of the European Union. Moreover, you will facilitate the certification process by QPs in the United Kingdom and Israel, ensuring compliance with U.S. standards.Your responsibilities will include conducting audits of Suppliers and Contract Service Providers across the European Economic Community and other regions, while closely monitoring any changes to European regulatory requirements. You will also host inspections conducted by the Health Product Regulatory Authority (HPRA) and other Competent Authorities within the European Union. As a key contributor to our annual Quality System reviews—including Quality Management Review (QMR) and Annual Product Reviews (APRs)—you will collaborate with our European CDMOs and assist in managing European Product Complaints.This position is based in our Dublin, Ireland office and will require up to 25% travel, which may include some international trips.Your primary responsibilities will encompass:Batch CertificationEnsuring all manufacturing and testing activities adhere to approved procedures, Investigational Medicinal Product Dossiers, and regulatory standards.Overseeing that outsourced manufacturing and testing activities comply with GMP regulations.
