15 jobs found in North Wales

Merck Job Description Our company is launching a highimpact global Supply Planning Transformation and seeking a Manufacturing Network Supply Planning Lead with a strongpharmaceutical or drug development manufacturingbackground to help shape how we plan and supply across a multisite network. In this role, you will lead theprocess and solution designof an enterprisewideAdvanced Planning System (APS), identifying and closing gaps in current supply planning practices, harmonizing ways of working across sites, and building scalable, futureready planning models. You will work endtoend-from design through deployment and hypercare-driving change adoption, elevating planning capabilities, and partnering with crossfunctional and global teams to deliver a stepchange in service, agility, and reliability for our global manufacturing network. This role is for a builder-someone who thrives in ambiguity, moves with speed, and brings the intensity required to reshape how we plan, operate,...

Merck Job Description In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Responsibilities : This position supports the design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission standards that can be used for drug and/or vaccine projects across all therapeutic areas.Adheres to standard operating procedures and guidelines established by the department. Drives data structures which includes analysis and reporting data standards and submission standards and actively contributes to the department's strategic initiatives....

Merck Job Description Our company is launching a highimpact global Supply Planning Transformation and seeking a Manufacturing Network Supply Planning Lead with a strongpharmaceutical or drug development manufacturingbackground to help shape how we plan and supply across a multisite network. In this role, you will lead theprocess and solution designof an enterprisewideAdvanced Planning System (APS), identifying and closing gaps in current supply planning practices, harmonizing ways of working across sites, and building scalable, futureready planning models. You will work endtoend-from design through deployment and hypercare-driving change adoption, elevating planning capabilities, and partnering with crossfunctional and global teams to deliver a stepchange in service, agility, and reliability for our global manufacturing network. This role is for a builder-someone who thrives in ambiguity, moves with speed, and brings the intensity required to reshape how we plan, operate,...

Merck Job Description Position Title Associate Principal Scientist Department Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious Disease Brief Description of Position The Regulatory Affairs Headquarters Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team. They will have excellent communication and collaboration skills and will work closely with a global liaison(s) to help develop and implement a global strategy for registration and/or maintenance of VID products. Responsibilities may encompass all aspects of planning and implementation of a global regulatory strategy and regulatory submissions including assisting in preparing submissions, protocol review, and conducting research on regulatory guidances or competitive intelligence. Primary activities include, but are not limited to: * Assists in regulatory agency communications and...

Merck Job Description In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Responsibilities : This position supports the design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission standards that can be used for drug and/or vaccine projects across all therapeutic areas.Adheres to standard operating procedures and guidelines established by the department. Drives data structures which includes analysis and reporting data standards and submission standards and actively contributes to the department's strategic initiatives....

Merck Job Description Role Summary The Specialist, Scientific Leader Contracting, Global Expert Management and Strategy (GEMS) Consulting and Medical Education, position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This position is responsible for the process and training oversight of the outsourced Global Support Team in support of GEMS Consulting and Medical Education programs. This position also manages the coordination of ad-hoc projects in support of data integrity and related tasks. The Specialist is responsible for running routine and ad-hoc reports and may also support a variety of short- and long-term department initiatives. Responsibilities and Primary Activities Collaborates and integrates with U.S. and Global Business, Legal, and Compliance teams to ensure alignment of the Scientific Leader (SL) contracting process with all applicable...

Merck Job Description The Executive Director has the primary responsibility for strategy, oversight, and delivery of end-to-end activities involving new or marketed drug(s) for oncology indications. The Executive Director leads the team responsible for the cross-functional delivery of critical milestones in an oncology asset's lifecycle, spanning discovery through reimbursement, integrating the scientific, commercial, and manufacturing aspects critical to delivering clinically beneficial medicines to the right patients. The key to success is bearing the primary responsibility for developing, aligning, executing, and communicating the overall asset strategy. Specifically, the Executive Director may be responsible for: Creation, alignment, execution, and adaptation of the asset strategy cross-functionally Lead the asset development team to maximize the asset's potential Identifying registrational opportunities for pre-clinical and early clinical candidates which...

Merck Job Description Position Title Associate Principal Scientist Department Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious Disease Brief Description of Position The Regulatory Affairs Headquarters Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team. They will have excellent communication and collaboration skills and will work closely with a global liaison(s) to help develop and implement a global strategy for registration and/or maintenance of VID products. Responsibilities may encompass all aspects of planning and implementation of a global regulatory strategy and regulatory submissions including assisting in preparing submissions, protocol review, and conducting research on regulatory guidances or competitive intelligence. Primary activities include, but are not limited to: * Assists in regulatory agency communications and...

Merck Job Description Role Summary The Specialist, Scientific Leader Contracting, Global Expert Management and Strategy (GEMS) Consulting and Medical Education, position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This position is responsible for the process and training oversight of the outsourced Global Support Team in support of GEMS Consulting and Medical Education programs. This position also manages the coordination of ad-hoc projects in support of data integrity and related tasks. The Specialist is responsible for running routine and ad-hoc reports and may also support a variety of short- and long-term department initiatives. Responsibilities and Primary Activities Collaborates and integrates with U.S. and Global Business, Legal, and Compliance teams to ensure alignment of the Scientific Leader (SL) contracting process with all applicable...

Merck Job Description The Executive Director has the primary responsibility for strategy, oversight, and delivery of end-to-end activities involving new or marketed drug(s) for oncology indications. The Executive Director leads the team responsible for the cross-functional delivery of critical milestones in an oncology asset's lifecycle, spanning discovery through reimbursement, integrating the scientific, commercial, and manufacturing aspects critical to delivering clinically beneficial medicines to the right patients. The key to success is bearing the primary responsibility for developing, aligning, executing, and communicating the overall asset strategy. Specifically, the Executive Director may be responsible for: Creation, alignment, execution, and adaptation of the asset strategy cross-functionally Lead the asset development team to maximize the asset's potential Identifying registrational opportunities for pre-clinical and early clinical candidates which...

Carter's, Inc. If you are a CURRENT Carter's employee, do not apply via this external application. Search "Browse Jobs" in Workday to apply internally. POSITION PURPOSE In partnership with the store team, the stock associate provides support for all aspects of shipping and receiving, stockroom organization, inventory control, and related housekeeping activities. The stock associate partners with the store team in execution of the replenishment process to ensure outstanding customer service and product placement. ESSENTIAL JOB FUNCTION (TASKS, DUTIES AND RESPONSIBILITES MOST IMPORTANT) Customer Focus: Maintains a strong and genuine customer focus on the sales floor. Monitors and adheres to all safety regulation and polices as directed by the company. Partners with the store team to maintain company standard of a neat, clean, and organized store. Contributes to and supports the team on delivering customer service consistently by engaging talent, encouraging...

Merck Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Medical Writer, , the review of accurate, clear, and compliant clinical, regulatory, and/or publicfacing documents in support of the company portfolio. The Medical Writer: Acquires and applies knowledge and understanding of medical writing responsibilities, including design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy). Demonstrates growing competence and independence in preparing clinical regulatory (e.g., clinical...

Merck Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Medical Writer, , the review of accurate, clear, and compliant clinical, regulatory, and/or publicfacing documents in support of the company portfolio. The Medical Writer: Acquires and applies knowledge and understanding of medical writing responsibilities, including design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy). Demonstrates growing competence and independence in preparing clinical regulatory (e.g., clinical...

Merck Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Medical Writer, , the review of accurate, clear, and compliant clinical, regulatory, and/or publicfacing documents in support of the company portfolio. The Medical Writer: Acquires and applies knowledge and understanding of medical writing responsibilities, including design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy). Demonstrates growing competence and independence in preparing clinical regulatory (e.g., clinical...

Merck Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Medical Writer, , the review of accurate, clear, and compliant clinical, regulatory, and/or publicfacing documents in support of the company portfolio. The Medical Writer: Acquires and applies knowledge and understanding of medical writing responsibilities, including design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy). Demonstrates growing competence and independence in preparing clinical regulatory (e.g., clinical...