62 pharmaceutical jobs found in West Point, PA

Merck Job Description We are seeking an experienced and innovative Associate Principal Scientist with a strong background in supporting in vitro pharmacology for early drug discovery to join the External Quantitative Biosciences group (ExQB). Under the broad direction of a Principal Scientist in ExQB, the candidate will support the execution of externalized In vitro biology projects across all discovery sites in our Research and Development division's disease areas, as well as participate in relationship management of Contract Research Organizations (CRO). The ideal candidate will be an experienced in vitro biology bench scientist and team player with experience supporting collaborations across a broad range of discovery biology disciplines. In collaboration with Quantitative Biosciences (QB), this individual will effectively assess and grow our external early discovery in vitro biology capabilities to drive pipeline support in line with our company's broader...

Merck Job Description Reporting to the Director of Packaging Commercialization, the Associate Director, Engineering, Packaging Commercialization will lead packaging development for new oral solid dosage and parenteral products in our small molecule portfolio. This role involves collaborating with stakeholders across the end-to-end continuum of CMC areas and requires both an understanding of packaging as well as prior experience developing and commercializing new products on cross-functional teams. The Associate Director will be accountable for the definition and execution of overall packaging strategies that meet global network needs. Responsibilities include ensuring packaging system designs are robust, packaging processes are efficient, and control strategies are integrated with both upstream and downstream needs. They will ensure activities supporting these program deliverables are executed with technical rigor and drive risk understanding and reduction prior to...

Merck Job Description We are seeking professionals with the following qualifications, skills and experience: The successful candidate will be responsible for the day-to-day oversight of the end to end operations management of assigned application portfolios. Further, the candidate will drive operations excellence through aherence to enterprise and organizational standards and industry leading practices. The ideal candidate will be techno-functional and comfortable in both technical and functional operations subject matter. Education Level: A bachelor's degree in IT/Computer Science, or a related field is preferred. However, candidates with proven expertise in IT operations, infrastructure management, and service delivery will also be considered without a formal degree. Industry certifications are highly valued as proof of practical knowledge and skills. Required Experience and Skills: 3+ years intermediate experience in IT Operations, infrastructure...

Merck Job Description The Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics (PDMB) function of our Research & Development Division in West Point, Pennsylvania, is seeking 2 dynamic and collaborative scientists for the Drug Metabolism and Pharmacokinetics (DMPK) group. The Associate Principal Scientist will be a key contributor to multi-disciplinary drug discovery and development efforts providing an integrated understanding of DMPK properties, pharmacokinetics/pharmacodynamics (PK/PD), and drug interaction (DDI) risk of novel therapeutics. The key responsibilities will be working on teams of highly collaborative, cross-functional scientists to discover and develop therapeutics across various modalities. The Associate Principal Scientist will design and interpret in silico, in vitro, and in vivo analyses to support the discovery of therapeutics with the desired DMPK profile. They will assess DDI risk using static mechanistic and/or physiologically based...

Merck Job Description The Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics (PDMB) function of our Research & Development Division in West Point, Pennsylvania, is seeking 2 dynamic and collaborative scientists for the Drug Metabolism and Pharmacokinetics (DMPK) group. The Associate Principal Scientist will be a key contributor to multi-disciplinary drug discovery and development efforts providing an integrated understanding of DMPK properties, pharmacokinetics/pharmacodynamics (PK/PD), and drug interaction (DDI) risk of novel therapeutics. The key responsibilities will be working on teams of highly collaborative, cross-functional scientists to discover and develop therapeutics across various modalities. The Associate Principal Scientist will design and interpret in silico, in vitro, and in vivo analyses to support the discovery of therapeutics with the desired DMPK profile. They will assess DDI risk using static mechanistic and/or physiologically based...

Merck Job Description We are seeking professionals with the following qualifications, skills and experience: The successful candidate will be responsible for the day-to-day oversight of the end to end operations management of assigned application portfolios. Further, the candidate will drive operations excellence through aherence to enterprise and organizational standards and industry leading practices. The ideal candidate will be techno-functional and comfortable in both technical and functional operations subject matter. Education Level: A bachelor's degree in IT/Computer Science, or a related field is preferred. However, candidates with proven expertise in IT operations, infrastructure management, and service delivery will also be considered without a formal degree. Industry certifications are highly valued as proof of practical knowledge and skills. Required Experience and Skills: 3+ years intermediate experience in IT Operations, infrastructure...

Merck Job Description Reporting to the Director of Packaging Commercialization, the Associate Director, Engineering, Packaging Commercialization will lead packaging development for new oral solid dosage and parenteral products in our small molecule portfolio. This role involves collaborating with stakeholders across the end-to-end continuum of CMC areas and requires both an understanding of packaging as well as prior experience developing and commercializing new products on cross-functional teams. The Associate Director will be accountable for the definition and execution of overall packaging strategies that meet global network needs. Responsibilities include ensuring packaging system designs are robust, packaging processes are efficient, and control strategies are integrated with both upstream and downstream needs. They will ensure activities supporting these program deliverables are executed with technical rigor and drive risk understanding and reduction prior to...

Merck Job Description We are seeking an experienced and innovative Associate Principal Scientist with a strong background in supporting in vitro pharmacology for early drug discovery to join the External Quantitative Biosciences group (ExQB). Under the broad direction of a Principal Scientist in ExQB, the candidate will support the execution of externalized In vitro biology projects across all discovery sites in our Research and Development division's disease areas, as well as participate in relationship management of Contract Research Organizations (CRO). The ideal candidate will be an experienced in vitro biology bench scientist and team player with experience supporting collaborations across a broad range of discovery biology disciplines. In collaboration with Quantitative Biosciences (QB), this individual will effectively assess and grow our external early discovery in vitro biology capabilities to drive pipeline support in line with our company's broader...

Merck Job Description Job Description: Our Digital Manufacturing Operations organization supporting the thriving West Point site is seeking a Process Automation Engineer (Specialist, Manufacturing Automation) to join the team. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and collaboration of individuals. To this end, we strive to create an environment of mutual respect, encouragement, and teamwork. As part of our team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. This role will provide automation system support and expertise to enable our manufacturing division in the reliable and compliant supply of quality vaccine products to customers and patients across the globe. Key responsibilities: Troubleshoot challenging equipment/automation issues and innovate to improve manufacturing performance Maintain the automation systems in...

Merck Job Description The Quality Environmental Monitoring (EM) Associate Director (P4) reports to EM Quality Lead and provides direct Quality support to operational areas as part of a Quality Integrated Production Team (IPT) Operating model for assigned E2E/IPTs. With guidance from Quality IPTs Leadership team, the Associate Director will ensure compliance and quality of products/processes and perform responsibilities to facilitate the release of product to the marketplace. Key Responsibilities: Accountable for the oversight and sustained state of environmental control per the Environmental Monitoring Plan for Classified Areas; performing job functions located in classified operational, Controlled Non-Classified areas and within office settings. Works closely with assigned End to End (E2E) of Operations, Quality, Deviation Management, Technical Operations, and other cross functional groups in overall team environment, and respectively as independent...

Merck Job Description The Associate Director- Device Tech Transfer is a leadership role within the Device Development and Technology Organization. This position is responsible for providing strategic program leadership, technical expertise, and project management in the scale-up, development, commercialization, and transfer of medical devices and combination products, with a focus on autoinjectors, prefilled syringes, and other drug delivery systems. The Associate Director will collaborate with a team of engineers and technical staff to support global and site-specific projects, facilitate technology transfer, and drive product robustness for sustained launch in alignment with the company's business goals, and quality and regulatory compliance. Essential Duties and Responsibilities: Program Leadership and Technical Project Management: Provide program leadership in the development, commercialization, and transfer and sustained launch of medical devices and...

Merck Job Description Senior Scientist/Engineer, Medical Device and Combination Products, Analytical The Center for Packaging & Device Analytics (CPDA), within our Manufacturing Division, has responsibility for applied physical, material & analytical science to support production and commercialization of product packaging and drug-delivery medical device/combination-products (MDCPs), such as auto-injectors and pre-filled syringes. We are an interdisciplinary engineering science Center of Excellence that supports the entire global-human-health portfolio and closely partner with various Packaging or Device Technology engineering groups, packaging sites, and partner analytical groups. The CPDA is located at our Company's large research and manufacturing West Point, PA location, where our packaging & device laboratories are established. The CPDA is seeking a Sr. Scientist/Engineer who, as an individual contributor, can focus on the following responsibilities...

Merck Job Description The Quality Environmental Monitoring (EM) Associate Director (P4) reports to EM Quality Lead and provides direct Quality support to operational areas as part of a Quality Integrated Production Team (IPT) Operating model for assigned E2E/IPTs. With guidance from Quality IPTs Leadership team, the Associate Director will ensure compliance and quality of products/processes and perform responsibilities to facilitate the release of product to the marketplace. Key Responsibilities: Accountable for the oversight and sustained state of environmental control per the Environmental Monitoring Plan for Classified Areas; performing job functions located in classified operational, Controlled Non-Classified areas and within office settings. Works closely with assigned End to End (E2E) of Operations, Quality, Deviation Management, Technical Operations, and other cross functional groups in overall team environment, and respectively as independent...

Merck Job Description The Ethics & Compliance Office (ECO) is accountable for our Company's ethics and compliance program. Reporting to the Director, ECO Corruption Data Risk Monitoring Program, the Senior Specialist will be part of a U.S.-based headquarters compliance team and play a key role in compliance risk monitoring, supporting global and/or regional efforts and executing Headquarter (HQ) monitoring activities as it relates to Human Health International ex-US activities. This position focuses on monitoring potential corruption risk through data analysis and reporting on a global level. In this role, you will: Be part of the team and support the development and sustainability of the risk monitoring program at the global level. Translate, understand and apply knowledge of anti-corruption risks, compliance policies, controls, and processes to execute compliance monitoring activities. Conduct data analyses on financial systems, customer event systems,...

Merck Job Description The Ethics & Compliance Office (ECO) is accountable for our Company's ethics and compliance program. Reporting to the Director, ECO Corruption Data Risk Monitoring Program, the Senior Specialist will be part of a U.S.-based headquarters compliance team and play a key role in compliance risk monitoring, supporting global and/or regional efforts and executing Headquarter (HQ) monitoring activities as it relates to Human Health International ex-US activities. This position focuses on monitoring potential corruption risk through data analysis and reporting on a global level. In this role, you will: Be part of the team and support the development and sustainability of the risk monitoring program at the global level. Translate, understand and apply knowledge of anti-corruption risks, compliance policies, controls, and processes to execute compliance monitoring activities. Conduct data analyses on financial systems, customer event systems,...

Merck Job Description The Position Our IT team operates as a business partner proposing ideas and innovative solutions that enable new organizational capabilities. We partner internationally to deliver the services and solutions that help everyone to be more productive and enable innovation. The Information Technology team at our Company's R&D division is looking for Product Analyst to support the Patient Safety and Quality & Compliance Product Line.The individual will be responsible to deliver high quality IT solutions/services, leveraging broad IT knowledge to transform business needs into IT requirements and deliver them with the larger IT team and vendors. Understanding of business strategy, goals, challenges/pain points, IT architecture, data platform, standard applications, and external environment changes is expected. What will you do? Build deep knowledge of Patient Safety systems and processes, especially those involving Veeva Vaults. Develop...

Merck Job Description Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. To ensure we receive high quality data from the investigational sites around the globe, our Clinical Research systems have to be compliant with regulatory requirements and follow our SDLC policy. Clinical Systems Quality Manager will be responsible to ensure our clinical systems are developed, validated and implemented while following high quality standards. Under the guidance of Head BEO and in collaboration with IT PM and Business System Owners the CSQM will oversee the quality and regulatory requirements of IT systems across Global Clinical Development (GCD), Global Regulatory Affairs & Clinical Safety (GRACS). This role is one of three core responsibilities...

Merck Job Description The Position Our IT team operates as a business partner proposing ideas and innovative solutions that enable new organizational capabilities. We partner internationally to deliver the services and solutions that help everyone to be more productive and enable innovation. The Information Technology team at our Company's R&D division is looking for Product Analyst to support the Patient Safety and Quality & Compliance Product Line.The individual will be responsible to deliver high quality IT solutions/services, leveraging broad IT knowledge to transform business needs into IT requirements and deliver them with the larger IT team and vendors. Understanding of business strategy, goals, challenges/pain points, IT architecture, data platform, standard applications, and external environment changes is expected. What will you do? Build deep knowledge of Patient Safety systems and processes, especially those involving Veeva Vaults. Develop...

Merck Job Description JobDescription: This position resides within our company's Value and Implementation (V&I), Outcomes Research Oncology organization, which is responsible for real-world evidence generation and outcomes research to enable sustained patient access to our company's innovations and improve patient health outcomes. Under the guidance of senior leaders, this individual will support the V&I, Outcomes Research teams in Hematology. Primary Responsibilities: Support the value evidence team in hematology and contribute to value evidence strategies for in-line and pipeline products. Serve as outcomes research representative on cross-functional regional and global teams. Critically assess drivers/barriers to reimbursement and market access, and identify relevant value evidence data gaps from clinical, medical, regulatory, payer/access, and marketing stakeholders to define integrated evidence generation plans. In collaboration with internal...