28 business development associate jobs found

Career Category Engineering Job Description ABOUT AMGEN   Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier,   fuller,   and longer. We discover, develop,   manufacture,   and deliver innovative medicines to help millions of patients. Amgen helped   establish   the biotechnology industry more than 40 years ago and   remains   on the   cutting-edge   of innovation, using technology and human genetic data to push beyond   what’s   known today.    ABOUT THE ROLE   Role   Description:    The   Specialist SAP Developer   will play a critical role   of an ABAP Developer   using ABAP on HANA   in the   GTS   system   with expert level hands-on   experience in F ORMS like SAPSCRIPT, SMARFORMS, ADOBE-FORMS, SAP Cloud ADS FORMS.   This individual will serve as a technical leader, architecting   c ompliant solutions and guiding...

Career Category Engineering Job Description ABOUT AMGEN   Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier,   fuller,   and longer. We discover, develop,   manufacture,   and deliver innovative medicines to help millions of patients. Amgen helped   establish   the biotechnology industry more than 40 years ago and   remains   on the   cutting-edge   of innovation, using technology and human genetic data to push beyond   what’s   known today.    ABOUT THE ROLE   Role   Description:    The   Specialist SAP Developer   will play the role of an   experienced SAP   ATTP   ABAP Developer with strong   expertise   in S/4HANA ABAP and SAP ATTP interface development. The ideal candidate will have hands-on experience in pharmaceutical serialization processes, HANA-based development, and integration between ATTP, S/4HANA, and external systems....

Career Category Engineering Job Description ABOUT AMGEN   Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier,   fuller,   and longer. We discover, develop,   manufacture,   and deliver innovative medicines to help millions of patients. Amgen helped   establish   the biotechnology industry more than 40 years ago and   remains   on the   cutting-edge   of innovation, using technology and human genetic data to push beyond   what’s   known today.    ABOUT THE ROLE   Role   Description:    The   Specialist SAP Developer   will play a critical role   of an ABAP Developer   in GTS (ABAP)   System with expert level hands-on   experience   in all RICEFW .   This individual will serve as a technical leader, architecting   c ompliant solutions and guiding development   teams . The   role   demands strong technical   depth and...

Career Category Engineering Job Description ABOUT AMGEN   Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier,   fuller,   and longer. We discover, develop,   manufacture,   and deliver innovative medicines to help millions of patients. Amgen helped   establish   the biotechnology industry more than 40 years ago and   remains   on the   cutting-edge   of innovation, using technology and human genetic data to push beyond   what’s   known today.    ABOUT THE ROLE   Role   Description:    The   Specialist SAP Developer   will play a critical role   of an ABAP Developer   using   ABAP   with in   OTC   and   PTS area s   in S / 4 .   This individual will serve as a technical leader, architecting   c ompliant solutions and guiding development team   The role   demands strong technical depth in   ABAP in   OTC...

Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. Are you ready to architect the future of customer care? Join us in Wrocław and help shape integrated, scalable solutions that connect systems, streamline processes and elevate the customer experience across our global contact centres. If you’re passionate about designing seamless integrations and enabling smarter service delivery, this is your opportunity to make a real impact. What will you be doing? As a Solution Architect – Customer Care, you’ll be at the forefront of transforming how we serve our customers. You’ll design and implement end-to-end solutions that support Order to Cash (O2C) processes in a global contact centre environment. Your work will span the integration of Salesforce Service Cloud, SAP S/4HANA, SAP CPI, EDI platforms and ESKER, enabling real-time data exchange and automation through robust API strategies. You’ll lead the development and support of...

Career Category Information Systems Job Description oin Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your...

As an Automation Engineer you will be responsible for d esigning, building and maintaining digital infrastructure platforms to drive innovation by making informed decisions using real-time data and information. A typical day might include, but is not limited to, the following: Designing and delivering end-to-end data solutions to meet our current and future needs Facilitating the smooth transition of projects from development into production environment Overseeing migration of data from legacy systems to new applications Acting as a subject matter expert and the technical go-to for the data integration solutions Becoming intimately familiar with the data model of the process systems Iterating and shipping ideas quickly with minimal direction Collaborating effectively with other functions and groups on the sites data strategy Reviewing requirements, specifications and technical design documents to provide timely and meaningful feedback...

Preclinical Operations (PCO) is seeking a dynamic Associate Manager, Preclinical Operations  to join the team.  Using program management knowledge and experience in the drug development industry, the successful candidate would provide operational and Project Management support to Preclinical Development (PCD) and Drug Safety & Pharmacometrics (DSP) for multiple assigned projects .  The successful candidate would also provide guidance and input to cross-functional project teams to enable projects to drive to completion. This role has a 3-day onsite minimum requirement in Tarrytown, NY. Relocation can be provided. A typical day as an Associate Manager looks like: Facilitates development and alignment of  integrated PCD/DSP cross-functional project deliverables, plans, timelines and  resources,to align with the overall project plan throughout the project lifecycle from preclinical through commercialization. Ensures effective execution of project plan to...

Regeneron is a leading global biotechnology company that uses the power of science to invent, develop and commercialize life-transforming medicines for patients with serious diseases. The Regeneron Information Technologies team is seeking candidates for the Associate Director, Directory Services Architecture position. This strategic leadership role demands deep technical expertise, vision, and exceptional people management skills. You will be responsible for collaborating on the establishment of the architectural, engineering, deployment, governance, and level 3 support of the Regeneron Directory Services infrastructure, as well as the Directory Services ecosystem and other related services. The Regeneron Directory Services Architect will be responsible for designing solutions for both cloud and on-premises systems. This role includes providing strategic and technical direction and support to internal team members. Key duties involve strategic planning, governance, and making...

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management activities and decisions including quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The PDML is a member of the Clinical Data Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. In this role, a typical day might include: Responsible for the overall success of the studies within a program(s) for Clinical Data Management (CDM). Maintains an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or...

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management activities and decisions including quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The PDML is a member of the Clinical Data Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. In this role, a typical day might include: Responsible for the overall success of the studies within a program(s) for Clinical Data Management (CDM). Maintains an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or...

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management activities and decisions including quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The PDML is a member of the Clinical Data Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. In this role, a typical day might include: Responsible for the overall success of the studies within a program(s) for Clinical Data Management (CDM). Maintains an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or...

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management activities and decisions including quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The PDML is a member of the Clinical Data Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. In this role, a typical day might include: Responsible for the overall success of the studies within a program(s) for Clinical Data Management (CDM). Maintains an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or...

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management activities and decisions including quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The PDML is a member of the Clinical Data Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. In this role, a typical day might include: Responsible for the overall success of the studies within a program(s) for Clinical Data Management (CDM). Maintains an overview of clinical program(s) status and issues and proactively communicates progress, risks,...

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management activities and decisions including quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The PDML is a member of the Clinical Data Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. In this role, a typical day might include: Responsible for the overall success of the studies within a program(s) for Clinical Data Management (CDM). Maintains an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or...

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management activities and decisions including quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The PDML is a member of the Clinical Data Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. In this role, a typical day might include: Responsible for the overall success of the studies within a program(s) for Clinical Data Management (CDM). Maintains an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or...

With guidance, an Associate Manager, Drug Development Program Management (DPM) uses program management knowledge and experience in the drug development industry to provide operational leadership and manage components of development program(s). You will contribute to the cross functional development team (Strategic Program Team) to develop strategic plans including goals, budgets, timelines and track the execution of these plans from preclinical through commercialization/lifecycle management.  This role has a 3-day onsite requirement in either Tarrytown, NY or Basking Ridge NJ. This role is not eligible to fully remote work. A typical day as an Associate Manager in DPM looks like: Project Planning and Execution: Assist in the development and maintenance of integrated project plans, timelines, and budgets for drug development programs. Plan, track and manage project milestones, dependencies and critical path through existing project management planning systems and...

The Associate Director, Systems Management is responsible for the strategic oversight and day-to-day management of systems that support the delivery of regulated documentation to business stakeholders. This role involves maintaining the electronic Document Management System (EDMS), acting as the Business Process Owner (BPO) for the EDMS workstream and workflows for Global Development, and collaborating with various departments to ensure the smooth operation and continuous improvement of these systems.   This role will lead the identification of EDMS data for reporting, analysis, and integration with other P&P software. In this role, a typical day might include: Strategic System Oversight and Day-to-Day Management: Provide strategic direction and oversight for systems that support the delivery of regulated documentation. Monitor system performance and address any issues that arise to minimize downtime and ensure continuous availability. Electronic Document...

Job Title Senior CRM (Salesforce) Specialist - Sleep and Respiratory Care (Murrysville, PA) Job Description Senior CRM (Salesforce) Specialist – Sleep and Respiratory Care Philips is currently recruiting a Senior CRM Specialist based in Murrysville, PA!  In support of our Customer Relationship Management system (Salesforce.com), you will facilitate the more tactical, day-to-day aspects of supporting, discovering, validating, documenting and communicating business-process-related knowledge through modeling, simulating and analyzing current and future states. Your role: Integration/migration and reporting elements of CRM using advanced knowledge of Microsoft and ensuring system is configured and maintained to support company business practices. Monitor and take corrective action related to the integration of SAP and CRM data; Works on continuous improvement and optimization of Sales Processes Positively impact the output of the sales organization; Contribute to the...

Career Category Quality Job Description Position Summary / Purpose This role is accountable for the end-to-end global process that ensures AI-enabled systems used in GxP contexts are validated/qualified and maintained in a state of control throughout their lifecycle, consistent with the company’s Quality Management System (QMS) expectations for global process ownership and controlled document architecture. This role is validation/qualification-specific and operates in partnership with the existing global Business Process Owner (BPO) for Responsible Use of AI for GxP, who owns overarching responsible-use governance and user controls (e.g., human-in-the-loop expectations and usage constraints) and good understanding on the Global AI Regulatory requirements (EU Act, FDA). Scope Applies to AI systems, models, and tools (standalone or embedded) used to generate information or data supporting GxP-regulated activities, including the validation pathway that...