Senior Regulatory Affairs Associate, EU & UK Market
Posted on Jul 13, 2026 by CV-Library
London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
Your new company
An established, research-driven generics pharmaceutical company with a strong presence across the UK and EU markets. The organisation offers a collaborative, team-oriented environment and is committed to delivering high-quality, affordable medicines while supporting employee development.
Your new role
As a Senior Regulatory Affairs Associate, you will support the lifecycle management of a diverse portfolio of generic medicinal products. You will be responsible for preparing and submitting regulatory dossiers (including MAAs, variations, and renewals) in line with MHRA and EMA requirements, as well as managing post-approval activities.You will liaise with regulatory authorities, respond to queries within agreed timelines, and ensure compliance of product labelling and documentation (SmPCs, PILs, artwork). The role also involves supporting regulatory strategy, tracking submission timelines, and monitoring evolving regulatory guidelines to assess business impact.
What you'll need to succeed
Degree in Life Sciences, Pharmacy, or a related field
Proven Regulatory Affairs experience within the pharmaceutical industry (generics preferred)
Strong knowledge of UK (MHRA) and EU regulatory frameworks
Experience with CTD/eCTD submissions and lifecycle management
Familiarity with variations and post-approval processes
Excellent organisational and communication skills
Ability to manage multiple projects in a fast-paced environmentWhat you'll get in return
Hybrid working (3 days onsite in London, 2 days remote)
Opportunity to work within a collaborative and supportive team
Exposure to a broad and varied generics portfolio across UK and EU markets
Career development and ongoing training opportunities
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career
An established, research-driven generics pharmaceutical company with a strong presence across the UK and EU markets. The organisation offers a collaborative, team-oriented environment and is committed to delivering high-quality, affordable medicines while supporting employee development.
Your new role
As a Senior Regulatory Affairs Associate, you will support the lifecycle management of a diverse portfolio of generic medicinal products. You will be responsible for preparing and submitting regulatory dossiers (including MAAs, variations, and renewals) in line with MHRA and EMA requirements, as well as managing post-approval activities.You will liaise with regulatory authorities, respond to queries within agreed timelines, and ensure compliance of product labelling and documentation (SmPCs, PILs, artwork). The role also involves supporting regulatory strategy, tracking submission timelines, and monitoring evolving regulatory guidelines to assess business impact.
What you'll need to succeed
Degree in Life Sciences, Pharmacy, or a related field
Proven Regulatory Affairs experience within the pharmaceutical industry (generics preferred)
Strong knowledge of UK (MHRA) and EU regulatory frameworks
Experience with CTD/eCTD submissions and lifecycle management
Familiarity with variations and post-approval processes
Excellent organisational and communication skills
Ability to manage multiple projects in a fast-paced environmentWhat you'll get in return
Hybrid working (3 days onsite in London, 2 days remote)
Opportunity to work within a collaborative and supportive team
Exposure to a broad and varied generics portfolio across UK and EU markets
Career development and ongoing training opportunities
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career
Reference: 225362640
https://jobs.careeraddict.com/post/113549300
Senior Regulatory Affairs Associate, EU & UK Market
Posted on Jul 13, 2026 by CV-Library
London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
Your new company
An established, research-driven generics pharmaceutical company with a strong presence across the UK and EU markets. The organisation offers a collaborative, team-oriented environment and is committed to delivering high-quality, affordable medicines while supporting employee development.
Your new role
As a Senior Regulatory Affairs Associate, you will support the lifecycle management of a diverse portfolio of generic medicinal products. You will be responsible for preparing and submitting regulatory dossiers (including MAAs, variations, and renewals) in line with MHRA and EMA requirements, as well as managing post-approval activities.You will liaise with regulatory authorities, respond to queries within agreed timelines, and ensure compliance of product labelling and documentation (SmPCs, PILs, artwork). The role also involves supporting regulatory strategy, tracking submission timelines, and monitoring evolving regulatory guidelines to assess business impact.
What you'll need to succeed
Degree in Life Sciences, Pharmacy, or a related field
Proven Regulatory Affairs experience within the pharmaceutical industry (generics preferred)
Strong knowledge of UK (MHRA) and EU regulatory frameworks
Experience with CTD/eCTD submissions and lifecycle management
Familiarity with variations and post-approval processes
Excellent organisational and communication skills
Ability to manage multiple projects in a fast-paced environmentWhat you'll get in return
Hybrid working (3 days onsite in London, 2 days remote)
Opportunity to work within a collaborative and supportive team
Exposure to a broad and varied generics portfolio across UK and EU markets
Career development and ongoing training opportunities
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career
An established, research-driven generics pharmaceutical company with a strong presence across the UK and EU markets. The organisation offers a collaborative, team-oriented environment and is committed to delivering high-quality, affordable medicines while supporting employee development.
Your new role
As a Senior Regulatory Affairs Associate, you will support the lifecycle management of a diverse portfolio of generic medicinal products. You will be responsible for preparing and submitting regulatory dossiers (including MAAs, variations, and renewals) in line with MHRA and EMA requirements, as well as managing post-approval activities.You will liaise with regulatory authorities, respond to queries within agreed timelines, and ensure compliance of product labelling and documentation (SmPCs, PILs, artwork). The role also involves supporting regulatory strategy, tracking submission timelines, and monitoring evolving regulatory guidelines to assess business impact.
What you'll need to succeed
Degree in Life Sciences, Pharmacy, or a related field
Proven Regulatory Affairs experience within the pharmaceutical industry (generics preferred)
Strong knowledge of UK (MHRA) and EU regulatory frameworks
Experience with CTD/eCTD submissions and lifecycle management
Familiarity with variations and post-approval processes
Excellent organisational and communication skills
Ability to manage multiple projects in a fast-paced environmentWhat you'll get in return
Hybrid working (3 days onsite in London, 2 days remote)
Opportunity to work within a collaborative and supportive team
Exposure to a broad and varied generics portfolio across UK and EU markets
Career development and ongoing training opportunities
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career
Reference: 225362640
Share this job:
Alert me to jobs like this:
Amplify your job search:
Expert career advice
Increase interview chances with our downloads and specialist services.
Visit Blog