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Sobre esta vaga de Director, Technical Leader na MSD

MSD · Presencial · CZE - Central Bohemian - Prague (IT Riverview)

Job Description

We are seeking a Technical Leader for data foundations in RaDS value team to ensure the frictionless flow of research data between data capture systems, between lab and archival systems / storage, and to establish initial master and reference data capabilities for early-stage research entities (e.g., small molecules, biologics). This role will drive engineering for application integration and lab data movement and storage from internal labs and CRO. This will also review current master and reference data needs in support of early research and establish capabilities to support these needs in collaboration with research platforms.


Key Responsibilities


  • Partner with product line leader to understand data movement and integration needs – between applications, between systems of record and systems of truth and from externals parties (CROs and data providers) to company network
  • Provide technical leadership to services that deliver application integrations and data integrations
  • Ensure reliable, secure, and scalable integration patterns using industry-standard tools and best practices
  • Ensure high-quality ingestion, schema evolution handling, lineage capture, and observability across pipelines.
  • Champion best practices for batch, micro-batch, and streaming ingestion where applicable
  • Own architecture, design, deployment, and operations of secure, auditable data transfer services to support inbound transfers from CROs and external data providers into the company network as well as transfers between internal storage locations
  • Leveraging enterprise capabilities, architect and design reference data management (RDM) capabilities that standardize and govern common vocabularies and reference tables used across discovery (e.g., reagent catalogs, instrument types, species/strain taxonomies, assay types).
  • Architect and design master data management (MDM) to support unique entity resolution and trusted master records for assets critical to discovery (samples, reagents, compounds, biological entities).
  • Provide architecture and engineering leadership for Application integration, data integration and data transfers
  • Act as a hands-on technical leader able to contribute to architecture, integration patterns, code reviews, and proof-of-concept work as needed.
  • Lead and/or support the standing up of GxP systems where applicable, ensuring compliance with quality standards, audit readiness, and data integrity (ALCOA+).
  • Communicate complex data concepts clearly to technical and non-technical stakeholders; drive alignment and decision-making.
  • Mentor and groom engineering leaders, fostering best practices in data management, SDLC, and compliance.

Qualifications


Education:

  • Bachelor’s or advanced degree in a basic science (e.g., biology, chemistry) or in computer science/engineering.

Experience:

  • 5+ years of experience in technical design and architecture leadership roles, particularly within the biopharma or healthcare sectors.
  • 7+ years of hands on and technical and architectural roles with application integration and data integration
  • Strong knowledge of current technologies supporting application and data integration
  • Strong hands on experience with cloud storage and compute infrastructure (e.g., AWS, Azure) and knowledge of automation and monitoring tools.
  • Familiarity with FAIR data principles and best practices related to data management and interoperability.
  • Strong experience with Agile methodologies and product management frameworks.
  • Demonstrated application of strong SDLC principles across the software delivery lifecycle (requirements, design, development, testing, deployment, operations).
  • Experience standing up and supporting GxP systems, with practical knowledge of data integrity, validation, and compliance frameworks.
  • Strong communication skills with the ability to translate scientific and technical requirements into actionable solutions.
  • Team-oriented mindset with experience mentoring and developing talent.
  • Familiarity with lab informatics and data platforms (e.g., ELN/LIMS, instrument integrations, data lake/repository concepts).
  • Understanding of metadata, ontologies, and research entity master data (e.g., molecules, biologics, assays).
  • Excellent leadership, communication, and stakeholder management skills.
  • Proven ability to motivate cross-functional teams and drive product strategy from conception to execution.

Preferred Qualifications (Nice to Have):

  • Experience in biopharma, biotech, or research organizations.
  • Hands-on exposure to ELN/LIMS systems and lab floor systems.
  • Experience with FAIR data principles and ontology-driven data management.

Additional location(s) Compensation Information:

Required Skills:

Agile Project Management, Agile Project Management, Agile Tools, Application Integrations, Applications Architecture, Conceptual Modeling, Data Access, Data Compliance, Data Ingestion, Data Integration, Data Management, Data Migrations, Data Security, Data Standards, Data Structures, Emerging Technologies, Integration Architecture, Methods and Tools, Requirements Management, Service Integration, Software Application Design, Software Development, Software Development Life Cycle (SDLC), Software Implementations, Software Interoperability {+ 4 more}

Preferred Skills:

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Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

11/4/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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Sobre a MSD

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. ​​

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