Reckitt

Regulatory Associate

Reckitt

full-time

Posted on:

Location Type: Office

Location: Hod HaSharonIsrael

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About the role

  • Ensuring that our new product developments meet global regulatory requirements with precision.
  • Act as a catalyst for change, using detailed knowledge to create comprehensive dossiers crucial for product registrations.
  • Navigate the intricate regulatory landscape to deliver products that enrich lives every day.

Requirements

  • Degree in a scientific field with a robust understanding of global regulatory environments impacting consumer products.
  • Experience in dossier creation, submission, and product lifecycle management.
  • A track record of reviewing and authoring high-quality documents.
  • Ability to deliver consistently under pressure, adhering to cost, time, and quality standards.
  • Familiarity with the regulatory requirements for medical devices in the EU (MDR) and US (510k) would be beneficial.
  • Commercially aware, adept at building partnerships and proposing improvements to enhance business processes.
  • Capable of embracing change and setting clear objectives in line with our business goals.
Benefits
  • We invest in the wellbeing of our people through parental benefits
  • Employee Assistance Program to promote mental health
  • Life insurance for all employees globally
  • Range of other benefits in line with the local market
  • Global share plans to save and share in Reckitt's potential future successes
  • Short-term incentives to recognise, appreciate and reward your work for delivering outstanding results
  • Rewarded in line with Reckitt's pay for performance philosophy

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
dossier creationproduct lifecycle managementdocument reviewdocument authoring
Soft skills
ability to deliver under pressurecommercial awarenesspartnership buildingchange managementobjective setting