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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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Executive Director, R&D Compliance, Global Medical and Scientific Affairs

Advise Merck’s global clinical development and medical affairs teams on pharmaceutical compliance. Oversee risk monitoring, policy implementation, senior counseling, and an international team of three.

USJungtinės ValstijosNJNaujasis DžersisPAPensilvanija
231 900 $ – 365 000 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųAtitiktis

Aprašymas

  • Advise Global Clinical Development and Value & Implementation stakeholders worldwide on compliance matters.
  • Join the Value & Implementation Extended Leadership Team and serve as the compliance contact for its organizational leader.
  • Set strategic direction for oversight, data monitoring, analysis, and risk-based recommendations.
  • Brief senior management on compliance matters and external developments that affect internal compliance needs.
  • Advise Value & Implementation, Human Health stakeholders, and business operations on inherent risks.
  • Promote compliant business practices through policy development, compliance communications, and corrective actions.
  • Work with the research division on its Compliance Monitoring Plan to identify and address potential risks.
  • Support due diligence for later-stage business development and integration of completed acquisitions.
  • Coordinate with the Ethics & Compliance Office and International Legal and Compliance on headquarters-led and cross-regional practices.
  • Lead and develop a three-person team based in the United States and Europe.
  • Develop strong teams and talent across the compliance organization.

Reikalavimai

  • Bachelor’s degree required.
  • At least 15 years of experience, with knowledge of laws, regulations, and policies governing pharmaceutical business practices, especially medical affairs.
  • Experience with advertising and promotion regulations, the Anti-Kickback Statute, and the Foreign Corrupt Practices Act.
  • Experience advising clients and influencing decision-makers, including senior leaders, on legal and compliance matters in life sciences.
  • Strong analytical ability to identify compliance risks and develop mitigation strategies.
  • Sound judgment, disciplined decision-making, emotional intelligence, and an effective advisory style.
  • Strong written and verbal communication and presentation skills.
  • Willingness to travel internationally as needed.
  • Ability to build collaborative relationships across functions, divisions, and regions.
  • Familiarity with research and human health organizations and their activities.
  • Experience developing or implementing written policies and guidance.
  • Experience leading and developing teams, or a strong interest in people management.
  • An advanced degree in science, business, or policy is preferred.
  • A JD from a US-accredited law school or an equivalent degree from outside the United States is strongly preferred.
  • Required skills include compliance program development, compliance reporting, cross-cultural awareness, attention to detail, ethical compliance, sound judgment, leadership, metrics analysis, people management, policy implementation, regulatory compliance audits, regulatory reporting, stakeholder management, technical documentation management, and training and development.

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).
  • Paid holidays.
  • Vacation leave.
  • Compassionate leave and sick days.
  • Hybrid work arrangement.

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CVS Health

CVS Health Business Compliance Manager, Requests for Information

CVS Health
Mažmeninė prekybaSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosALAlabamaAZArizonaCTKonektikutasFLFloridaKSKanzasasKYKentukisLALuizianaNJNaujasis DžersisNCŠiaurės KarolinaOHOhajasOKOklahomaPAPensilvanijaRIRod AilandasTNTenesisTXTeksasas
66 330 $ – 145 860 $ / metai
HibridinisVisas etatasVyresnysis specialistasVadovasPrivaloma Kalba: anglųAtitiktis

Oversee regulatory information requests across CVS Health operations and jurisdictions. Lead analysts and coordinate compliant responses with Legal, Compliance, and Operations.

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Senior Regulatory Affairs Manager, Biomaterials

Johnson & Johnson
H1B vizos rėmėjasBiotechnologijaFarmacijos produktaiSveikatos priežiūra
USJungtinės ValstijosMAMasačusetsasPAPensilvanija
117 000 $ – 201 250 $ / metai
HibridinisVisas etatasVyresnysis specialistasVadovasPrivaloma Kalba: anglųAtitiktis

Lead regulatory strategy for Johnson & Johnson Orthopaedics’ biomaterials, biologics, and combination product programs. Oversee submissions, due diligence, and regulatory support for external innovation partnerships.

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Senior Manager, Regulatory Affairs – Biomaterials | Johnson & Johnson

Johnson & Johnson
H1B vizos rėmėjasFarmacijos produktaiSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosMAMasačusetsasPAPensilvanija
117 000 $ – 201 250 $ / metai
HibridinisVisas etatasVyresnysis specialistasVadovasPrivaloma Kalba: anglųAtitiktis

Lead regulatory strategy for biomaterials, biologics, and combination products at Johnson & Johnson Orthopaedics. Guide submissions, external innovation reviews, and global approvals from development through product lifecycle management.

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RhyGaze

Reguliacinių operacijų direktorius | RhyGaze | Filadelfija, hibridinis darbas

RhyGaze
BiotechnologijaFarmacijos produktaiSveikatos priežiūra
USJungtinės ValstijosPAPensilvanijaHibridinisVisas etatasVadovasPrivaloma Kalba: anglųAtitiktis
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