WhatsApp Group Join Now
Telegram Group Join Now
      

Position Name :

Regulatory Affairs Specialist

Organization :

Straive

Qualification:

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Experience:

1 to 2 Years

Salary:

25,000 - 35,000 /month

Location:

Work From Home

As a Regulatory Affairs Specialist at Straive, you will be responsible for regulatory research and compliance, particularly for US and Canada regulations. This remote position involves interpreting regulations, summarizing them concisely, and producing regulatory summaries and news. You will need to have a strong background in legal/regulatory compliance and excellent analytical, research, and writing skills.

Qualifications

  • Skills: Research Skills, Regulatory Compliance, Analytical Skills, Writing Skills, Organizational Skills
  • Experience:
    • 2+ years of experience in regulatory compliance or EHS/Chemicals management regulatory affairs
    • Experience with regulatory compliance for US & Canada Chemicals Inventory (EPA related topics for industrial hazardous chemicals) and GHS for the Chemical Industry
    • Minimum 2+ years of SDS/EHS regulatory/legal experience; expertise in chemical product safety, customer support, and supplier communication for US and Canada
  • Education: Degree in Chemistry, Chemical Engineering, Biology, or related disciplines
  • Language Proficiency: Excellent comprehension in reading English documents and fluency in oral and written English

Application Link

Featured Courses

1

CLINI INDIA

Interactive Brokers Logo

Coupon:

CLINIBHARAT (10% Discount)

Courses:

  • Data Management
  • Pharmacovigilance
  • Medical Writing
  • Medical Coding
  • Regulatory Affairs
  • Clinical Research
2

CLINIVERSITY

Interactive Brokers Logo

Coupon:

MONSSOON (20% Discount)

Courses:

  • Data Management
  • Pharmacovigilance
  • Medical Coding
  • Clinical Research
3

CLINIWINGS

Interactive Brokers Logo

Coupon:

WINGS (10% Discount)

Courses:

  • Clinical Data Management
  • Pharmacovigilance
  • Medical Writing
  • Regulatory Affairs
  • Clinical Research