Senior Regulatory Associate: Global Pharma Compliance

Pfizer Inc.; England; On-site; GBP 60,000 - 90,000; Full time

Job summary

Pfizer Inc. is seeking regulatory affairs professionals to support development, maintenance, and compliance for medicinal products and medical devices in the UK.

You will work with national regulators, ensure accurate labeling and regulatory documentation, and assist with approvals for unlicensed medicines as needed. The role emphasizes strong written and verbal communication, analytical thinking, and a proven regulatory track record, with eligibility to work in the United Kingdom.

Qualifications

• Life sciences or chemistry degree with honors; MSc/PhD preferred.
• Professional regulatory qualifications desirable (e.g., MSc in Regulatory).
• Proven experience and track record in Regulatory (Human Medicinal Products).
• Excellent written and verbal communication skills.
• All applicants must have authorization to live and work in the UK.

Responsibilities

• Support regulatory activities for development and maintenance of medicines and medical devices as applicable.
• Obtain NRA approvals for supply of unlicensed medicines (Named Patient/Compassionate Use).
• Maintain regulatory databases and ensure compliance in packaging and prescribing information updates.
• Support MA divestments, MA cancellations, product discontinuations and supply continuity.
• Contribute to Good Regulatory Practice (GRP) and regulatory group development.

Skills

Regulatory knowledge

Regulatory submissions

Communication skills

Analytical thinking

Education

Life sciences/chemistry degree

Master's/PhD or regulatory qualification

Tools

Computer literacy

Job description

Pfizer Inc. is seeking regulatory affairs professionals to support development, maintenance, and compliance for medicinal products and medical devices in the UK.

You will work with national regulators, ensure accurate labeling and regulatory documentation, and assist with approvals for unlicensed medicines as needed. The role emphasizes strong written and verbal communication, analytical thinking, and a proven regulatory track record, with eligibility to work in the United Kingdom.