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Pfizer
Pfizer
H1B vizasi homiysiFarmatsevtika mahsulotlariKonsaltingMarketing
Pfizer — butun umr davomida salomatlikni qo‘llab-quvvatlaydigan dori-darmonlar va tibbiy xizmatlarni ishlab chiqish hamda taqdim etishga e’tibor qaratadigan global farmatsevtika kompaniyasi. Uning faoliyati ilmiy innovatsiyalar bilan bir qatorda xavfsiz, samarali va hamyonbop davolash usullaridan foydalanish imkoniyatini kengaytirishni ham qamrab oladi; kompaniya saraton va boshqa jiddiy sog‘liq muammolariga qarshi davolash usullarini rivojlantirishga alohida ahamiyat beradi. Kompaniya faoliyati farmatsevtika tadqiqotlari, sog‘liqni saqlash va ularga aloqador tijoriy funksiyalarda karyera izlayotgan mutaxassislar uchun qiziq bo‘lishi mumkin.
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Kompaniyadagi ish o‘rinlari

Senior Associate Scientist, GMP Investigations and Compliance

Support Pfizer’s medicines and vaccines by strengthening GMP investigations and compliance across R&D sites. Write investigations, assist with audits, and use quality data to drive improvements.

USAmerika Qo‘shma ShtatlariMAMassachusetsMOMissuri
68 600 $ – 114 300 $ / yil
GibridTo‘liq stavkaSeniorTalab Qilinadigan Til: inglizchaMuvofiqlik

Tavsif

  • Prepare clear, timely investigations using Pfizer quality systems.
  • Check investigations against applicable quality and compliance standards.
  • Encourage consistent use of root cause analysis and human error reduction methods.
  • Assist with internal and external audits and inspections, coordinating requests and responses.
  • Assess compliance with global procedures.
  • Review compendia and regulatory requirements.
  • Take part in internal quality forums.
  • Evaluate investigation, audit, and inspection data to identify, recommend, and implement improvements.
  • Select solutions for moderately complex issues and follow procedures under general guidance.
  • Help meet work group objectives and collaborate with colleagues.
  • Manage priorities to meet project deadlines and contribute as a team member.

Talablar

  • Bachelor’s degree in microbiology, molecular biology, biochemistry, or a related field and at least three years of GMP microbiology laboratory experience; alternatively, an MBA or MS and at least one year of experience.
  • Advanced technical writing ability.
  • Strong documentation skills and careful attention to detail.
  • Experience working in Good Manufacturing Practices (cGMP) settings.
  • Experience with GMP microbiology investigations.
  • Experience with laboratory data platforms such as LIMS, eQMS, and GDMS.
  • Ability to work effectively with peers and leaders on cross-site, multidisciplinary teams.
  • Ability to find relevant information in scientific literature.
  • Ability to manage timelines and deliverables independently.
  • Strong organizational skills and demonstrated attention to detail.
  • Experience using common AI tools, including generative tools such as ChatGPT or Microsoft Copilot, to solve problems and improve productivity.
  • Curiosity about how AI tools can improve outcomes, along with understanding of responsible AI practices, including risk management and ethical use.
  • Must be authorized to work in the United States for any employer.
  • U.S. work visa sponsorship is unavailable for this role, now and in the future.
  • Permanent U.S. work authorization is required.

Imtiyozlar

  • 401(k) plan with Pfizer matching contributions.
  • Additional Pfizer retirement savings contribution.
  • Paid vacation, holidays, and personal days.
  • Paid caregiver, parental, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.
  • Relocation support may be offered depending on business needs and eligibility.
  • May participate in Pfizer’s Global Performance Plan, with a bonus target of 7.5% of base salary.

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Medical Device Regulatory Affairs Manager

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H1B vizasi homiysiIshlab chiqarishSog‘liqni saqlashTibbiy sug‘urta
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Senior Regulatory Affairs Manager, Biomaterials

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

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

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H1B vizasi homiysiFarmatsevtika mahsulotlariSog‘liqni saqlashTibbiy sug‘urta
USAmerika Qo‘shma ShtatlariMAMassachusetsPAPensilvaniya
117 000 $ – 201 250 $ / yil
GibridTo‘liq stavkaSeniorYetakchiTalab Qilinadigan Til: inglizchaMuvofiqlik

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.

Ochish