Hub Submission Manager

Talentmark; Stone Cross; Hybrid; GBP 20,000 - 29,000; Part time

Job summary

Talentmark is recruiting for a Hub Submission Manager, joining a pharmaceutical company on a 6-month contract. The role is hybrid, based in Sandwich, Kent, with 2–3 days on-site per week.

You will oversee day-to-day regulatory submissions to Health Authorities across allocated countries, plan submissions, coordinate with product teams, manage translations, and ensure timely delivery. A strong eye for detail, experience with electronic submissions, and solid project management are essential.

Qualifications

• Experience working in a busy regulated environment with tight deadlines.
• Hands-on experience building electronic submissions in the pharmaceutical industry.
• A good understanding of regulatory guidelines and how a submission is put together.
• Great attention to detail, strong organisation and a talent for project management.
• A keen interest in learning new software and tools, and a team player attitude.

Responsibilities

• Looking after the day to day running of regulatory submissions to Health Authorities in your allocated countries.
• Planning each submission and making sure it is ready on time.
• Working closely with product teams and country contacts to agree what is needed and when.
• Building, sending and storing electronic and paper submissions.
• Managing translations and keeping everyone up to date on timelines.
• Spotting problems early and helping to fix them, so that deadlines are met.

Skills

Regulatory submissions

Project management

Attention to detail

Team player

Learning new software

Job description

Talentmark are recruiting for a Hub Submission Manager to join a company in the pharmaceutical industry on a contract basis for 6 months. This role is hybrid working in Sandwich, Kent 2 to 3 days per week.

Salary

Up to £17.67 per hour (PAYE). Rate are dependant upon experience.

Hub Submission Manager Role

• Looking after the day to day running of regulatory submissions to Health Authorities in your allocated countries.
• Planning each submission and making sure it is ready on time.
• Working closely with product teams and country contacts to agree what is needed and when.
• Building, sending and storing electronic and paper submissions.
• Managing translations and keeping everyone up to date on timelines.
• Spotting problems early and helping to fix them, so that deadlines are met.

Your Background

• Experience working in a busy, regulated environment with tight deadlines.
• Hands-on experience building electronic submissions in the pharmaceutical industry.
• A good understanding of regulatory guidelines and how a submission is put together.
• Great attention to detail, strong organisation and a talent for project management.
• A keen interest in learning new software and tools, and a team player attitude.

Company

Our client is one of the world’s premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

It is essential that applicants hold entitlement to work in the UK.

Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.