drjobs Regulatory Affairs - Senior Associate

Regulatory Affairs - Senior Associate

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1 Vacancy
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Job Location drjobs

London - UK

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Job Title: Regulatory Affairs Senior Associate

Job Location: London UK

Job Location Type: Hybrid

Job Contract Type: Fulltime

Job Seniority Level: Associate

At Perrigo we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions Accessible to All. We are proud to be a Top 10 player in the European Consumer SelfCare market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best SelfCare for Everyone we are the people behind the brands you trust. We are Opill® Compeed® Solpadeine® NiQuitin® ACO® and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to a blendedbranded business to win in selfcare.

Description Overview

We are hiring a talented Senior Regulatory Affairs Associate who will be responsible for the handson regulatory activities associated with maintaining the portfolio of branded products within the Perrigo UKIE business.

Our office is in central London.

Scope of the Role

  • Work as part of a multifunctional team by providing regulatory input to new product development and associated supporting documentation complete due diligence on time for any assigned product dossiers.
  • As part of the team ensure product registrations are correct and compliant with the relevant legislation. Establish review approve and update regulatory documentation
  • Prepare and publish packages and submit MAA’s and variations to meet the business needs via the electronic platforms
  • Maintain accurate and complete records by updating the relevant trackers product folders and regulatory databases
  • Approve Artwork and Texts from a regulatory perspective
  • Participate in project meetings with both internal and external contacts
  • Communicate with local regulatory authorities regarding license applications and variations
  • Interpret and implement legislation follow changes in national regulations and legislations and proactively manage impact of these changes
  • Support marketing and sales with claims creation and copy review as per internal guidelines
  • Carry out other related regulatory affairs duties as required

Experience Required

Our ideal candidate should have a minimum of 3 years’ experience in Regulatory Affairs working with OTC medicines including Post Marketing License Maintenance activities renewals and safety updates.

You should be familiar with working in CCsystems (e.g. TrackWise) and eCTD publishing tools.

The person we are looking for should be:

  • Selfmotivated flexible and open to changing requirements
  • Highly driven with enthusiasm to meet requirements and cope under demanding pressure
  • The ability to work autonomously and in a team
  • The ability to support several concurrent activities
  • Excellent communication in English
  • Excellent problemsolving skills
  • Being thorough focused and detail oriented

Benefits

We believe our people are our greatest asset. Alongside competitive compensation we offer benefits tailored to supporting you and your family as well as career development opportunities to ensure you feel valued and supported both professionally and personally.

Find out more about Total Rewards at Perrigo.

Hybrid Working Approach

We love our offices and the setting they provide for inperson collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too so we promote flexibility with the ability to work two days a week from home in many roles.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or other characteristics protected by law. #weareperrigo


Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech and IT domains.

For more details and to find similar roles please check out the below Lifelancer link.

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Employment Type

Full Time

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