Director

• Define and execute a global strategy for biologic critical reagents across the Large Molecule product lifecycle.
• Establish governance, policies, and procedures for reagent selection, qualification, characterization, release, change control, storage, distribution, and disposal.
• Drive reagent lifecycle management, including change control, comparability assessments, requalification, and retirement.
• Lead a team responsible for qualification of cell banks, reference materials, in-house standards, and assay controls.
• Ensure reagent quality and fitness-for-purpose through adherence to acceptance criteria, stability programs, compliance standards, and ongoing monitoring.

Director, Quality Control

Account Executive

• Builds and maintains trust with colleagues, stakeholders, and customers through effective communication, integration, and collaboration
• Ability to lead through challenging and ambiguous situations while ensuring that deadlines and objectives are met
• Ability to influence others and lead without authority during complex situations, fostering collaborative problem-solving and reaching consensus
• Experience in navigating diverse teams or stakeholders to achieve common goals
• Understands applicable product portfolio to provide approved disease and product information to key decision makers and stakeholders within account(s)
• Leads Our Company's efforts to maximize appropriate utilization of its portfolio while bringing resources to customers that contribute to better outcomes for patients
• Knowledge of account ecosystem and current emerging market and business trends impacting assigned accounts
• Establishes strategic approach to the account in alignment with approved guidance from the marketing teams

National Account Director, Payer/PBM Segment

QA Engineer

• Provide quality oversight of device assembly and packaging operations
• Serve as on-site quality oversight for medical device and combination product operations requiring above-site support
• Accountable for coordinating Device Quality and Regulatory triage and root cause investigation of deviations impacting device assembly and packaging operations
• Provides oversight of CAPA for device assembly and packaging operations including CAPA approval, performance of effectiveness checks and CAPA metric monitoring
• Builds strong partnerships with site Operations, Packaging Technical Operations, Validation, Global DQ&R, and other functions to ensure seamless execution of device quality activities
• Represents Device Quality and Regulatory for device related internal and external audits

Associate Director, Device Quality Assurance

Procurement

• Lead sourcing for Equipment & Automation categories globally, ensuring alignment with business objectives.
• Develop and implement category strategies that deliver cost savings, mitigate risk, and drive innovation.
• Conduct market intelligence, competitive analysis, and supplier benchmarking to identify best-in-class solutions.
• Engage with Equipment Management Teams and project stakeholders to understand requirements and translate them into sourcing strategies.
• Facilitate stakeholder meetings, tier reviews, and routine updates to ensure alignment and transparency.
• Build and maintain strong relationships with key suppliers and internal partners across regions.
• Establish and maintain Supplier Relationship Management programs, including KPIs, scorecards, and regular business reviews.
• Monitor supplier performance and implement continuous improvement initiatives.
• Prepare detailed pre-negotiation plans and lead complex negotiations to secure optimal commercial terms.
• Draft, review, and execute contracts in collaboration with Legal and ensure compliance with corporate standards.
• Identify, track, and deliver cost reduction opportunities, including managing Purchase Price Variance (PPV).

Equipment & Automation Procurement Manager

• Provides leadership for the successful implementation of SDTM (Study Data Tabulation Model) data deliverables required for analysis, reporting, and regulatory submission
• Advises to ensure study data deliverables are compliant with regulatory agency requirements and expectations
• Accountable for a team of CDISC (Clinical Data interchange Standards Consortium) data standards experts
• Sets the strategic and operating direction for the SDSQM SC team
• Collaborates effectively with stakeholders at all levels in Biostatistics, Clinical Research, Data Management, Regulatory Affairs, and IT
• Leads a team of submission consultants with varying levels of expertise
• Has accountability and oversight for esubmission deliverables, and strategic and department responsibilities
• Stays current with regulatory guidance and submission standards and is a recognized leader providing specific clinical development and analysis & reporting deliverables domain expertise to stakeholders and staff at all levels
• Performs managerial and administrative duties including hiring, retention & engagement, coaching, mentoring, and people development
• Applies domain and management expertise to set and achieve operational and strategic objectives within a group, manages broad initiatives, and leads and actively contributes to departmental objectives
• Plays a role in developing and accomplishing priorities and objectives to align with the division scorecard
• Promotes good stewardship of company resources

Director, Statistical Programming - SDSQM

• Ensure Human Health has an industry‑leading strategy for sourcing, creating, and activating commercial data assets
• Own accountability for managing US data privacy and compliance risks associated with data access and use
• Partner with various stakeholders to extract maximum commercial value from data assets
• Oversee US data needs assessments by gathering input from analytics and business stakeholders
• Lead acquisition of new external assets and internal initiatives to capture additional US first-party data

Executive Director, US Data Strategy

Recruitment

• Execute heavy configuration within the Workday application, specifically focusing on Recruiting and Talent modules.
• Support and configure third-party talent acquisition systems, including Phenom People and Ajinga.
• Support, assess, and manage new business requests, recommending alternative technical solutions to improve HR/HRIS processes.
• Partner closely with HR Technology Process and Solutions leads, Global Centers of Excellence (COEs), and Operations Teams.
• Apply technical expertise to resolve complex business problems independently and collaboratively.

Senior Workday Recruiting – Talent Technology Specialist

Business Development Rep

• Collaborating closely with our company's research scientists, management, legal and external partners to negotiate material transfers, licenses, evaluations, consortia, research collaborations and other agreements to establish external scientific partnerships
• Negotiating with external counterparts to execute appropriate agreements in a timely manner in support of our Research Division objectives and compliance policies
• Educating and influencing our Research Division scientists and management in the executional and relational aspects of external partnering
• Participation and networking at industry-academia professional events to establish our Research Division as a partner of choice

Associate Director, Business Development – Discovery Transactions

Marketing

• Lead the end-to-end planning, coordination, and execution of ophthalmology congress activities, ensuring alignment with marketing and scientific priorities.
• Translate scientific strategy into operational congress plans, including product theater, booth design, scientific engagement activities, and stakeholder interactions.
• Guide logistical planning and vendor coordination to support pre-, during-, and post-congress deliverables, ensuring scientific quality, compliance, and execution excellence.
• Execute medical education initiatives aligned with the Ophthalmology scientific strategy, including branded and unbranded medical education (IME) programs for various scientific exchange platforms.
• Collaborate with internal and external stakeholders to identify unmet educational needs and deliver high-quality, evidence-based educational content.
• Engage external scientific experts, KOLs, and medical societies to ensure relevance, credibility, and excellence of educational deliverables.
• Define and monitor congress and medical education KPIs and success metrics with robust post-event analysis to inform future strategy and maximize impact.
• Serve as a strategic partner to Scientific Strategy leadership, providing input on congress and integrated medical education needs and prioritization.
• Collaborate with key stakeholders across the enterprise including Medical Affairs, Outcomes Research, Global Marketing, Clinical, Regulatory, Communications, Legal/Compliance to ensure cohesive, data-driven communication objectives and operational plans.
• Partner with fellow colleagues to invest in each other’s development, build a culture of inclusivity, psychological safety, transparency and stretch our collective team’s thinking by challenging the status quo for the purpose of creating stronger outcomes.

Associate Director, US Marketing – Ophthalmology Scientific Strategy

• Develop global payer pricing and access strategy, and value proposition for key pipeline assets, ensuring access considerations are integrated into global access plans and taking informed positions related to price, value and affordability challenges at the appropriate time of product development and launch.
• Partner closely with the cross functional team including marketing and Product Development Teams (PDTs), (ex. clinical, OR and medical affairs), regional and country teams to ensure patient access objectives and strategy are linked to clinical development, commercial and value evidence plans.
• Synthesize and communicate payer customer insights to inform current and future access strategy, including access opportunities and risks by country archetype. This includes conducting payer market research and analysis of payer landscape and competition.
• Co-lead with V&I the 4th hurdle framework assessments to inform access strategy and evidence generation plans.
• Develop global pricing strategy, product value scenarios and negotiation strategies in support of Global, Regional, Country plans.
• Collaborate with Regional access, pricing and affordability solutions teams within GMAx to inform access strategy development.
• Provide access assumptions into business development assessments on an ad-hoc basis.
• Collaborate with Policy colleagues in the assessment of and development of action plan to shape the value frameworks and other policies impacting value assessment.
• Lead the development of value communication resources, including payer value deck and other access resources.

Director, Global Market Access – PAH & Rare Diseases

Full-stack Engineer

• Work side by side with the Product Owner to assess the requirements, feasible solutions and implement configurations and enhancements to benefit scientific users of on prem and SaaS solutions
• Design and implement integrations between Sample, Reagent and Inventory managed systems and other systems using RESTful APIs and integration frameworks.
• Write clean, maintainable code and conduct thorough testing (unit, integration, end-to-end) to ensure software quality.
• Participate in code reviews, providing constructive feedback and documentation for technical processes and solutions.
• Collaborate with Product Analysts and stakeholders to translate business requirements into technical specifications.
• Ensure compliance with regulatory standards (GxP, FDA, HIPAA) and maintain data integrity throughout the software lifecycle.
• Continuously learn and adapt to new technologies, scientific concepts, and regulatory changes to enhance software solutions.
• Work within a matrix organizational structure, reporting to both the functional manager and the Product manager.
• Participate in Product planning, execution, and delivery, ensuring alignment with both functional and Product goals.

Senior Specialist, Software Engineering

Risk

• Develop and execute a comprehensive data governance strategy aligned with DSCS Digital’s business objectives and regulatory requirements.
• Lead the design and implementation of data governance frameworks, including data stewardship, data quality management, metadata management, and data lifecycle policies.
• Lead and harmonize CMC data strategy efforts across our Research & Development Division, our Manufacturing Division, IT, Quality and other relevant stakeholders to ensure an enterprise approach to data.
• Oversee data policy creation, enforcement, and ongoing education to ensure enterprise-wide adoption and compliance.
• Report on key data governance metrics, risks, and opportunities to executive leadership and relevant committees.
• Champion a culture of data-driven decision making and continuous improvement throughout the organization.

Senior Director, Data Governance – DSCS Digital

• Developing and managing strategic business relationships with Cardinal Healthcare, larger regional distributors, emerging specialty distributors, and emerging specialty/digital pharmacies
• Leading the account management efforts and supports the appropriate access for and utilization of our company's products
• Collaborating closely with cross-functional teams, including the Order Management Center, Manufacturing Division, Supply Chain, Field Sales, Payer and Brand Marketing, and other internal partners
• Developing and overseeing account and business plans for the full product portfolio
• Identifying areas of mutual opportunity with customer organizations, focused on improving patient outcomes and leveraging customer capabilities
• Partnering with leadership and headquarters teams to support negotiation of Distribution Service Agreements (DSAs)

National Account Director – Pharmacy, Distribution, Specialty Markets

• Translate and execute the vision for digital enablement, data strategy, and in silico capabilities across Development Sciences & Clinical Supply (DSCS) and related functions.
• Influence enterprise-level digital strategy and ensure alignment with business objectives.
• Serve as a multi-team leader who leads and mentors teams specializing in data engineering, data science, software development, and predictive analytics.
• Foster a collaborative environment that encourages innovation and continuous improvement.
• Oversee the design, implementation, and optimization of modern, automated, and contextualized data pipelines.
• Guide the creation of advanced data visualization platforms and dashboards to support decision-making and enhance data-driven insights.
• Champion the development and deployment of in silico modeling, AI/ML-enabled experiment design, and predictive analytics platforms.
• Identify and implement digital opportunities that drive operational efficiencies and reduce reliance on traditional experimentation.
• Develop and implement change management strategies to ensure developed digital solutions realize maximum value in DSCS.
• Provide clear elucidation of the business value being realized through DSCS Digital efforts.

Executive Director, Digital Insights

• Responsible for driving execution of value & Implementation and medical affairs plans for Gynecological Cancer in the region
• Guides country Research Division GMSA staff to execute the annual scientific & medical plan for gynecological cancer
• Chairs the Regional Medical Affairs Team (RMAT) to ensure execution of agreed medical tactics and leverage best practices
• Ensures scientific exchange is aligned with the global scientific communications platform
• Partners with regional Commercial, regional Outcomes Research, regional Policy and regional Market Access to drive development and execution of regional plans
• Consolidates actionable medical insights
• Engages with a network of scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies)
• Supports, as regional TA expert, affiliates staff in engagement with their national scientific leaders
• Organizes regional expert input events to answer company questions regarding how to implement new indications: advisory boards and group input meetings.

MSD