Senior Manager Regulatory Affairs

Blackfield Associates is looking for a Senior Manager Regulatory Affairs

Job description

Senior Regulatory Affairs Manager – Europe

A European‑focused regulatory role supporting the development, registration, and lifecycle management of speciality, orphan, paediatric, and generic medicines.


Key Responsibilities

  • Develop and execute EU regulatory strategies for innovative, speciality, and complex products.
  • Review non‑clinical and clinical data packages and identify gaps for regulatory submissions.
  • Lead/assist with MAAs, variations, line extensions, renewals, and post‑approval commitments.
  • Support regulatory interactions, including scientific advice and dossier due diligence (Modules 1–5).
  • Coordinate registrations across centralised, DCP, MRP, and national procedures.
  • Provide input across cross‑functional development teams and oversee documentation systems.
  • Support EU launch requirements and guide junior team members where needed.


Required Experience

  • Experience with ophthalmology products (eye drops, ophthalmic solutions).
  • Experience leading Health authority interactions and scientific advice meetings
  • Knowledge of medical devices/combination products, ideally ophthalmic.
  • Proven background in injectable/sterile products and related regulatory submissions.
  • Strong EU regulatory experience including MAAs, DCP/MRP, lifecycle management, and scientific advice.
  • Understanding of requirements for placing medicines on the EU market.
  • Hands on, proactive regulatory with authoring and submission experience


Skills & Qualifications

  • Degree in Pharmacy, Life Sciences, or similar.
  • Proficient with regulatory tools (eCTD publishing, CESP, MHRA Portal, etc.).
  • Strong analytical, communication, and project‑management capabilities.
  • Must be a proven regulatory SME in speciality pharma


Due to the nature of this roles hands-on, fast pace work, this role is not suitable for Regulatory Project Manager or those who have not directly authored dossier and lead review of both clinical and non clinical data package. All applicants must have clearly demonstrated experience with health authority interaction as an active/ leading member of meetings.


Hybrid based from Slough SL1.

Extra information

Status
Open
Education Level
Secondary School
Location
Slough
Type of Contract
Full-time jobs
Published at
09-03-2026
Profession type
Retail
Full UK/EU driving license preferred
No
Car Preferred
No
Must be eligible to work in the EU
No
Cover Letter Required
No
Languages
English

Slough | Retail Jobs | Full-time jobs | Secondary School

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