Remote Global Regulatory Affairs Lead

Placements24; East London; Hybrid; ZAR 1,996,000 - 2,994,000; Full time

Benefits offered by this job

Competitive salary

Bonuses

Remote work

Health insurance

Retirement planning

Job summary

Placements24 is seeking a seasoned Pharmaceutical Affairs Manager to lead global regulatory strategies from a fully remote setting. You will manage regulatory submissions, ensure compliance, and contribute to the worldwide product strategy while coordinating with cross‑functional teams.

The ideal candidate holds a Master’s or PhD in a related field, 7+ years of regulatory affairs experience with global submissions, and exceptional remote collaboration and leadership skills.

Qualifications

• Master's degree or Ph.D. in Pharmacy, Chemistry, Biology, or related field.
• 7+ years in pharmaceutical regulatory affairs with global submissions.
• Proven ability to lead cross-functional teams remotely.

Responsibilities

• Develop and execute global regulatory strategies for product development and commercialization.
• Prepare, review, and submit regulatory dossiers to health authorities worldwide.
• Act as main contact for regulatory agencies and facilitate approvals.
• Ensure ongoing compliance with national and international regulations.
• Provide regulatory guidance to R&D, manufacturing, and commercial teams.
• Lead regulatory intelligence and post-approval activities.
• Mentor junior regulatory professionals in a remote team.
• Collaborate with international counterparts to harmonize strategies.

Skills

Regulatory strategy

Global submissions

Remote leadership

CTD knowledge

Regulatory intelligence

Stakeholder management

Regulatory compliance

Education

Master's or PhD in Pharmacy

Tools

CTD eCTD systems

Regulatory databases

Job description

Placements24 is seeking a seasoned Pharmaceutical Affairs Manager to lead global regulatory strategies from a fully remote setting. You will manage regulatory submissions, ensure compliance, and contribute to the worldwide product strategy while coordinating with cross‑functional teams.

The ideal candidate holds a Master’s or PhD in a related field, 7+ years of regulatory affairs experience with global submissions, and exceptional remote collaboration and leadership skills.