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MSD
MSD
H1B vizos rėmėjasBiotechnologijaLogistikaSveikatos priežiūra

MSD yra pasaulinė biofarmacijos bendrovė, kurianti vaistus ir vakcinas svarbiausioms sveikatos problemoms spręsti, įskaitant vėžį, infekcines ligas, širdies ir kraujagyslių bei medžiagų apykaitos sutrikimus, taip pat daug dėmesio skirianti prevencinei priežiūrai. Jungtinėse Amerikos Valstijose, Kanadoje ir Puerto Rike MSD žinoma kaip „Merck & Co., Inc.“. MSD derina mokslinius tyrimus su kūrimo ir komercine kompetencija, kad sveikatos priežiūros sprendimai pasiektų žmones ir gyvūnus.

Bendrovės veikla apima žmonių sveikatą, gyvūnų sveikatą bei mokslinius tyrimus ir plėtrą, todėl galimybių atsiveria įvairių sričių specialistams – nuo mokslo, klinikinės ir komercinės veiklos iki operacijų bei įmonės funkcijų. Įvairiuose pasaulio regionuose veikianti MSD karjera atspindi jos dėmesį moksliniams tyrimams, bendradarbiavimui, įtraukčiai ir atsakingai pasaulinės sveikatos pažangai.

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Darbai įmonėje

Director of Digital Tech Transfer and Knowledge Management

Lead digital technology transfer and process knowledge management for biopharmaceutical manufacturing. Guide data-rich products, AI governance, and teams working across global operations.

USJungtinės ValstijosNCŠiaurės KarolinaPAPensilvanijaVAVirdžinija
173 200 $ – 272 600 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius

Aprašymas

  • Set the product vision and strategic roadmap for digital technology transfer and process knowledge management.
  • Lead and mentor product analysts, technology specialists, and process specialists.
  • Guide digital manufacturing products supporting technology transfer from concept and requirements through launch and ongoing improvement.
  • Connect Science & Technology, Research, Commercialization, manufacturing operations, and IT to turn business needs into scalable, compliant digital solutions.
  • Integrate data from systems such as MES, LIMS, and process controls into a unified process knowledge ecosystem.
  • Establish data integrity and governance practices that keep process data reliable, accurate, and inspection-ready.
  • Manage the product backlog and prioritize features according to business value and strategic priorities.
  • Report progress to executive stakeholders.
  • Ensure digital solutions meet GxP and internal quality standards.
  • Work with external contract manufacturing organizations to digitize technology transfer and create secure, standardized, compliant process data exchanges.

Reikalavimai

  • Bachelor's degree in engineering, computer science, life sciences, or a related discipline.
  • At least 10 years of relevant industry experience.
  • Demonstrated experience supporting pharmaceutical technology transfer and preparing receiving sites, including transferring process knowledge, assessing capabilities, preparing data, and handing operations over.
  • Experience in product management, program leadership, or a strategic role delivering large-scale, data-intensive digital products.
  • Experience managing and developing technical and cross-functional teams.
  • Strong communication and stakeholder management skills.
  • In-depth knowledge of biopharmaceutical manufacturing, technology transfer, and related data and control systems, including MES, DeltaV, PKM, Databricks, SCADA, and PI.
  • Ability to translate business objectives into detailed technical execution plans.
  • Experience implementing and scaling AI in mission-critical, highly regulated settings with governance, reliability, security, and compliance controls.
  • Preferred: direct experience implementing or managing PKM systems and digital technology transfer solutions.
  • Preferred: familiarity with advanced analytics and machine learning in manufacturing.
  • Preferred: experience with Agile development methods.
  • Preferred: strong background in process analytics (PPA/PPM) and GMP/GxP compliance.
  • Applicants must reside in the United States or Puerto Rico.
  • Visa sponsorship is not available.
  • Relocation is not available.
  • Regular employee status.

Privalumai

  • Annual bonus and long-term incentive, where applicable.
  • Medical, dental, vision, and other insurance coverage for employees and their families.
  • Retirement benefits, including a 401(k) plan.
  • Paid holidays.
  • Vacation leave.
  • Compassionate and sick leave.
  • Hybrid work arrangement.
  • Travel up to 10%.

Susiję darbai

Johnson & Johnson

Director, Pharmacovigilance Alliance Contracting and Management

Johnson & Johnson
H1B vizos rėmėjasFarmacijos produktaiSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosNJNaujasis DžersisPAPensilvanija
150 000 $ – 258 750 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius

Lead Johnson & Johnson’s global pharmacovigilance alliance contracting team and oversee agreement strategy, negotiation, and execution. Guide partnership governance, risk and compliance, team development, and process improvement.

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Elevance Health

Clinical Programs Director, Oncology and Cardiovascular Care

Elevance Health
H1B vizos rėmėjasB2BSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosCTKonektikutasMAMasačusetsasNJNaujasis DžersisNYNiujorkasVAVirdžinija
115 200 $ – 198 720 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius

Lead whole-person oncology and cardiovascular programs for Elevance Health’s national accounts. Build Centers of Excellence networks and advise major healthcare clients on care solutions.

Atidaryti