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Marsh McLennan
Marsh McLennan
H1B vizos rėmėjasFinansaiRinkodaraTeisė
„Marsh McLennan“ yra pasaulinė profesionalių paslaugų įmonė, teikianti konsultavimo paslaugas rizikos valdymo, strategijos ir su žmonėmis susijusiose srityse. Įmonių grupei priklauso draudimo tarpininkavimo ir rizikos valdymo paslaugas teikianti „Marsh“, perdraudimo ir kapitalo strategijų srityje besispecializuojanti „Guy Carpenter“, sveikatos, turto ir karjeros konsultavimo paslaugas teikianti „Mercer“ bei strategijos, ekonomikos ir prekių ženklų konsultavimo srityse besispecializuojanti „Oliver Wyman“. „Marsh McLennan“ visame pasaulyje dirba daugiau nei 85 000 darbuotojų, o įmonė sutelkia finansų, konsultavimo, rinkodaros ir kitų susijusių profesionalių paslaugų kompetencijas. Įmonės įdarbinimo sritys apima klientų konsultavimą, rizikos analizę, verslo strategiją, konsultavimą ir veiklos komandas palaikančias pareigas visose keturiose įmonėse.
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Darbai įmonėje

National Employee Health and Benefits Compliance Consultant

Advise Marsh McLennan Agency clients on U.S. employee health and benefits compliance. Support compliance education, training, research, and client presentations.

USJungtinės Valstijos
89 500 $ – 166 900 $ / metai
HibridinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųAtitiktis

Aprašymas

  • Support the Health and Welfare Compliance Services team with guidance, education, and training on federal, state, and local health and welfare benefits laws
  • Respond to a range of ad hoc compliance questions
  • Help write and peer review articles and presentations
  • Take part in client seminars and other public speaking engagements
  • Help develop intellectual capital for MMA, its clients, and prospective clients

Reikalavimai

  • Bachelor’s degree (BA/BS) from an accredited college or university, or an equivalent recognized institution
  • Juris Doctor degree from an accredited U.S. law school
  • Active license to practice law in at least one U.S. jurisdiction
  • At least three years of experience focused on U.S. health and welfare benefits law, including ERISA, the Internal Revenue Code, and the Affordable Care Act
  • Strong understanding of employer-sponsored group health and fringe benefit programs
  • Demonstrated ability to work both with a team of compliance specialists and independently with limited supervision
  • Ability to read and interpret statutes, regulations, and related technical guidance and materials
  • Ability to define problems, gather data, establish facts, and draw sound conclusions, seeking support from senior HaWCS staff when needed
  • Ability to draft written materials and business correspondence for non-specialist audiences, with support from senior HaWCS staff
  • Ability to help present information and respond to questions in group and one-on-one settings

Privalumai

  • Generous paid time off, including personal and volunteer leave
  • Tuition reimbursement and professional development opportunities
  • Remote work
  • Charitable contribution matching programs
  • Stock purchase opportunities
  • Health and welfare benefits
  • Tuition assistance
  • 401(k) savings and other retirement programs
  • Employee assistance programs
  • Performance-based incentives may be available

Susiję darbai

Biogen

Senior Manager, Global Regulatory Affairs at Biogen

Biogen
5 001 – 10 000 Darbuotojai
H1B vizos rėmėjasBiotechnologijaGamybaSveikatos priežiūra
USJungtinės ValstijosCAKalifornija
140 000 $ – 187 250 $ / metai
HibridinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųAtitiktis
Vault

Support regulatory strategy and submissions for Biogen’s biotechnology programs, including IND, CTA, NDA, and BLA filings. Coordinate health authority responses, labeling, and submission execution with global and cross-functional teams.

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Medtronic

Medical Device Regulatory Affairs Manager

Medtronic
H1B vizos rėmėjasGamybaSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosCTKonektikutasMAMasačusetsas
120 800 $ – 181 200 $ / metai
HibridinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųAtitiktis

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 vizos rėmėjasGamybaSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosCTKonektikutasMAMasačusetsas
120 800 $ – 181 200 $ / metai
HibridinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųAtitiktis

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

Atidaryti