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Role Filled

Senior Regulatory Affairs Executive

Pharmaceutial & Biotechnolgy
Technical Specialist
Regulatory
Luton
£40,000 - £45,000
Generic product (off patent/off brand)

Role Overview

The primary task for this position is to prepare regulatory documentation (Pre and Post authorisation) for submissions to regulatory authorities.

Company Information

Zenopa has partnered with a manufacturer of generic pharmaceutical products throughout the UK and Europe.

Role Requirements

– Support existing and new launches.
– Review and approval of artworks for EU and UK market.
– Provide technical support for change management, investigation CAPA identification and related activities at contract manufacturing sites.
– Support the maintenance of regulatory files and tracking databases.

Person Specifications

– Regulatory experience within the UK and EU market.
– Generics experience would preferable.

Package

Competitive base
Private medical insurance
Private dental insurance

Locations

Dunstable
Leighton Buzzard
Luton
Previous Listing
Date Updated
04 Sep 2024
Job reference
73459
Categories
Full Time
Permanent
Take Experience
This role has been filled
Hiring contacts
Tom B 3x4 2024
Tom Bruton
This role has been filled
Why Zenopa?

We aim to operate and maintain the following set of core values

Group people cartoon
01

We liaise on your behalf

Required equipment, e.g. cars, laptops, mobiles, we negotiate with the employer source and manage these on your behalf.

02

Solid Industry Relationships

Our recruitment teams have built relationships with some of the UK’s most prestigious pharmaceutical companies

03

High Success Rate

Our structured recruitment approach allows us to deliver consistently successful outcomes for both clients and candidates, supporting long-term placements and repeat partnerships.

04

Systems that work for you

As an ISO 9000 organisation we have fully defined systems that are regularly audited. You can be assured we consistently following processes that deliver for all.