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Johnson & Johnson
Johnson & Johnson
H1B vizasi homiysiBiotexnologiyaFarmatsevtika mahsulotlariSog‘liqni saqlash
Johnson & Johnson farmatsevtika, tibbiy qurilmalar va iste’molchilar salomatligi yo‘nalishlarida faoliyat yurituvchi global sog‘liqni saqlash kompaniyasidir. Uning tadqiqot va mahsulotlarni ishlab chiqish faoliyati onkologiya, immunologiya, neyrofanlar va kardiopulmonologiya yo‘nalishlaridagi dori vositalari hamda davolash usullarini, shuningdek yurak-qon tomir kasalliklarini davolash, ortopediya, jarrohlik va ko‘rish sohasi uchun MedTech yechimlarini qamrab oladi. Kompaniyaning keng qamrovli faoliyatiga salomatlik va farovonlik bo‘yicha ma’rifiy ishlar, yirik ko‘lamli ishlab chiqarish, investorlar bilan ishlash hamda global ijtimoiy ta’sir tashabbuslari ham kiradi. Bu faoliyatlar ilmiy, klinik, muhandislik, ishlab chiqarish, tijoriy va korporativ funksiyalarda imkoniyatlar yaratadi.
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Kompaniyadagi ish o‘rinlari

Senior Regulatory Affairs Manager, Biomaterials

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

USAmerika Qo‘shma ShtatlariMAMassachusetsPAPensilvaniya
117 000 $ – 201 250 $ / yil
GibridTo‘liq stavkaSeniorYetakchiTalab Qilinadigan Til: inglizchaMuvofiqlik

Tavsif

  • Shape regulatory strategies for biomaterials, biologics, combination products, and externally sourced innovations.
  • Advise on regulatory considerations early in development and contribute to due diligence and business development.
  • Guide products through development, clinical programs, submissions, approvals, launch preparation, and lifecycle management.
  • Direct regulatory engagements with agencies around the world.
  • Oversee Regulatory Affairs work, set priorities, and explain objectives, risks, and recommendations.
  • Prepare and maintain BLAs, IDEs and supplements, PMAs and supplements, 510(k)s, De Novo requests, HDEs, annual reports, global change notifications, and technical documentation.
  • Set regulatory direction for pipeline programs, clinical development, and global launch readiness.
  • Collaborate with R&D, Quality, Clinical, Medical Affairs, Supply Chain, Commercial, Business Development, and other partners.
  • Use independent judgment to resolve complex regulatory matters and deliver key regulatory work.
  • Guide Regulatory Affairs colleagues and cross-functional teams through daily coaching and technical advice.
  • Create and deliver training on regulatory, CMC, CGMP, biologics, combination product, and clinical investigation requirements.
  • Coordinate communications with global and regional or local regulatory agencies.
  • Keep company policies, procedures, and practices aligned with regulatory requirements.
  • Support approval and clearance efforts, identifying capability gaps and ways to address them.
  • Lead regulatory screening and technical diligence for external innovation, partnerships, licensing, acquisitions, and business development.
  • Represent the Biomaterials External Innovation regulatory function in governance forums, partner discussions, diligence, and agency engagements.

Talablar

  • Bachelor’s degree or higher in a scientific, engineering, pharmacy, or other relevant technical field.
  • At least eight years of relevant experience in medical devices, biologics, pharmaceuticals, combination products, or another regulated healthcare industry.
  • Demonstrated experience supporting complex product development programs.
  • Specialized knowledge of Chemistry, Manufacturing, and Controls (CMC) and Current Good Manufacturing Practice (CGMP) requirements.
  • Experience creating and carrying out regulatory strategies aligned with business objectives.
  • Direct experience developing, submitting, or maintaining BLAs and IDEs is strongly preferred.
  • Experience evaluating early-stage external innovations, conducting regulatory diligence, and supporting partnerships or business development is strongly preferred.
  • Expertise in biologics, biomaterials, combination products, CMC, CGMP, BLA, and IDE requirements.
  • Strong written and verbal communication skills.
  • Ability to work effectively with cross-functional stakeholders and external partners.

Imtiyozlar

  • Consolidated retirement pension plan.
  • 401(k) savings plan.
  • Long-term incentive program.
  • 120 hours of vacation per calendar year.
  • 40 hours of sick time per calendar year; 48 hours for Colorado residents and 56 hours for Washington residents.
  • 13 paid holidays per calendar year, including floating holidays.
  • Up to 40 hours of work, personal, and family time per calendar year.
  • 480 hours of parental leave within one year of a child’s birth, adoption, or foster placement.
  • Bereavement leave: 240 hours for an immediate family member or 40 hours for an extended family member per calendar year.
  • 80 hours of caregiver leave in a rolling 52-week period.
  • 32 hours of volunteer leave per calendar year.
  • 80 hours of military spouse time off per calendar year.
  • Hybrid work arrangement.

O‘xshash ish o‘rinlari

Medtronic

Medical Device Regulatory Affairs Manager

Medtronic
H1B vizasi homiysiIshlab chiqarishSog‘liqni saqlashTibbiy sug‘urta
USAmerika Qo‘shma ShtatlariCTKonnektikutMAMassachusets
120 800 $ – 181 200 $ / yil
GibridTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaMuvofiqlik

Lead regulatory strategy, submissions, and compliance for Medtronic medical devices, with a focus on U.S. and EU approvals. Guide the Stapling Regulatory Affairs team and work across product development and business functions.

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Medtronic

Regulatory Affairs Manager, Medical Devices — Medtronic (Hybrid, North Haven, CT)

Medtronic
H1B vizasi homiysiIshlab chiqarishSog‘liqni saqlashTibbiy sug‘urta
USAmerika Qo‘shma ShtatlariCTKonnektikutMAMassachusets
120 800 $ – 181 200 $ / yil
GibridTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaMuvofiqlik

Lead regulatory submissions, approvals, and compliance for Medtronic’s Surgical Operating Unit. Guide regulatory teams and cross-functional product strategies across the product lifecycle.

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CVS Health

CVS Health Business Compliance Manager, Requests for Information

CVS Health
Chakana savdoSog‘liqni saqlashTibbiy sug‘urta
USAmerika Qo‘shma ShtatlariALAlabamaAZArizonaCTKonnektikutFLFloridaKSKanzasKYKentukkiLALuizianaNJNyu-JersiNCShimoliy KarolinaOHOgayoOKOklaxomaPAPensilvaniyaRIRod-AylendTNTennessiTXTexas
66 330 $ – 145 860 $ / yil
GibridTo‘liq stavkaSeniorYetakchiTalab Qilinadigan Til: inglizchaMuvofiqlik

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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MSD

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

MSD
H1B vizasi homiysiBiotexnologiyaLogistikaSog‘liqni saqlash
USAmerika Qo‘shma ShtatlariNJNyu-JersiPAPensilvaniya
231 900 $ – 365 000 $ / yil
GibridTo‘liq stavkaYetakchiTalab Qilinadigan Til: inglizchaMuvofiqlik

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.

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