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Role Filled

Deputy Manager Reg Affairs

Pharmaceutial & Biotechnolgy
Technical Specialist
Regulatory
Luton (hybrid)
£46,000 - £53,000
Generic product (off patent/off brand)

Role Overview

The primary role of this individual is to compile regulatory submissions. This position requires a professional with good organisational and communication skills

Company Information

We are currently supporting a Pharma SME client who are expanding their team, and specialise in Generic medication

Role Requirements

– Full lifecycle management
– Change control management
– MA Submissions, renewals, variations
– Agency Management
– Work across UK/EU Markets

Person Specifications

– Experience dealing with Generic medication is desirable
– Regulatory Affairs experience (2 years+)

Package

Private Medical Insurance
Dental Insurance
Life assurance
Pension: 7% employer

Locations

Dunstable
Leighton Buzzard
Luton
Previous Listing
Date Updated
20 Feb 2025
Job reference
73629
Categories
Full Time
Permanent
Take Experience
This role has been filled
Hiring contacts
Katie g 2025
Katie Ginger
Expertise: Animal Health, Consumer Healthcare, Pharmaceutical
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.