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Senior Regulatory Affairs Specialist

Life Sciences
Regulatory Affairs
Master
Senior (7+)
Location
Puurs-Sint-Amands, Antwerp
Work type
Consultancy
Work model
Fulltime, On-site

Our client, a prominent pharmaceutical organization, is seeking an experienced professional to lead regulatory activities within the Benelux region. The role focuses on ensuring the quality and compliance of regulatory data and processes while managing marketing authorizations for medicinal products.

Responsibilities

  • Manage the preparation, submission, and follow-up of registration dossiers, renewals, and variation dossiers for medicinal products.
  • Lead the initiation, review, and implementation of label and artwork changes to ensure full compliance with regional regulations.
  • Provide strategic regulatory expertise to internal stakeholders and participate in launch planning and business unit meetings.
  • Support complex projects including marketing authorization transfers and legal entity changes across the regional market.
  • Draft and review local and global SOPs, work instructions, and other quality-related documentation.
  • Oversee the handling of CPP and ancillary document requests for emerging markets and maintain internal regulatory databases.
  • Coordinate with production plants and hubs to manage out-of-stock notifications and artwork approvals.

Requirements

  • You have a Bachelor’s degree in a scientific or related discipline.
  • You bring 8+ years of experience in regulatory affairs, conformance, or compliance within the pharmaceutical industry.
  • You possess advanced knowledge of EU and global regulatory procedures, marketing authorizations, and drug development practices.
  • You have experience working in a GMP environment and utilizing regulated document management tools.
  • You’re an organized and analytical professional with strong skills in technical writing and stakeholder influencing.
  • You have a perfect command of Dutch with good knowledge of English.

Nice to Haves

  • Master's, MBA, or PhD in a scientific field.
  • Experience with advanced digital regulatory systems and innovative compliance solutions.

Offer

  • Enjoy a competitive salary package with extra perks that recognize your talent.
  • Advance your career with a clear growth path, coaching, and mentoring to support you.
  • Thrive in a dynamic and supportive environment where you can truly make an impact.
  • Work when and where you perform best, ensuring an optimal work-life balance.
  • Choose a flexible transport solution, from a company car to a public transport subscription.
  • Expand your network and enjoy unforgettable moments at exclusive events and afterworks.
  • Grow your skills with external courses and our in-house Pauwels Academy.
  • Work on exciting projects with industry leaders in Life Sciences, Engineering & Digital.
  • Seize opportunities at every level, from a strong start to career acceleration and expert collaboration.
# 103187
With a plus sign and country code (e.g. +32 400 00 00 00).
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Candidates must be legally authorised to work in the EU and possess the required language skills for the job location.
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