Regulatory Affairs Project Manager (Rotterdam, NL, 3062 CE)

Rotterdam, Netherlands Type not listed
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Perrigo is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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 Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone , we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, 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 win in self-care.

Description Overview

Are you an experienced Regulatory Affairs Project Manager with business acumen and a keen eye for detail?

We are looking for a new colleague to reinforce the regulatory activity required to submit, approve and launch new products and the maintenance of existing commercialized products and dossiers. In this role, you will be a key advisor to internal teams and external stakeholders, contributing to successful product registrations and market access projects, promotional campaigns, and protection of existing products in a fast changing regulatory environment.

Scope of the Role

•    Assist in execution of regulatory activities per the project plan to assure new products meet submission, approval and commercial launch goals.

•    Highly involved in the products’ lifecycle, including New Product Development (NPD) and launches, lifecycle maintenance and promotional activities.

•    Support manufacturing and procurement in the management of change to existing commercial products.

•    Maintain product labeling in compliance with local and EU laws and regulations; develop and approve label specifications in compliance with SOPs.

•    Support the development and approval of packaging materials in a timely manner.

•    Process change requests in compliance with GMPs and regulations.

•    Maintain regulatory files and data systems in compliance with SOPs.

•    Ensure timely and effective communication and collaboration with other departments including marketing, CS&I (trade marketing), sales and corporate regulatory and innovation.

•    Review technical documentation and manage regulatory submissions in a timely manner.

•    Process feedback from regulatory authorities and notified bodies.

•    Support the development and clearance of promotional materials.

•    Provide input for analysis of data and/or management review, if required.

•    Assist in the process of reporting and investigating critical non-conformities and opportunities for improvement.

Experience Required

Master’s degree in Life Sciences, Foods, Pharmacy, or a related field

•    At least 4 years of experience in Regulatory Affairs

•    In-depth knowledge of local and EU regulations; at least in one of the countries of the Benelux and one or more of the following regulatory frameworks: medicines, medical devices, food supplements, biocides, general health products or cosmetic products.

•    Strong communication and project management skills

•    The ability to work both autonomously in local and international teams

•    Strong communication, persuasion and problem-solving skills, with the ability to translate regulatory complexity to non-regulatory employees

•    Curiosity - An eager and quick learner willing to develop and improve

•    Fluent in Dutch and English is a must; knowledge of French and German is an asset

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 in-person 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.) All application materials, including resumes and CVs, must be submitted in English. 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

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Job details

Seniority
Manager
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Rotterdam, Netherlands
Employment type
Not listed

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 184 comparable Manager Regulatory Affairs roles across 59 biopharma companies.

184Comparable roles tracked
177Currently active
59Companies hiring similar roles
29Countries represented

Salary context

57 of 184 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Manager CMC Regulatory Compliance · Merck KGaA $77,800/yr – $116,700/yr
Peer group range $97,250 – $219,500 (median $180,500)

Where these roles are based

Top locations among the 184 comparable roles

United States81
India14
Japan13
United Kingdom12
Poland12
China9

+ 23 more countries

Seniority mix

184 of 184 peers have a known seniority level

Manager136
Associate Director40
Associate8

Therapeutic area mix

22 of 184 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology10
Neuroscience5
Dermatology & Aesthetics3
Immunology3
Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Amgen Europe B.V. Breda, Netherlands Manager
Same function Same seniority Same country
45%similar
Lilly Shanghai, Shanghai, China Manager
Same function Same seniority
45%similar
AbbVie Maidenhead, ENGLAND Manager
Same function Same seniority
45%similar
AbbVie Maidenhead, ENGLAND Manager
Same function Same seniority
45%similar
AbbVie Singapore, sg Manager
Same function Same seniority
45%similar
AbbVie Taipei, tw Manager
Same function Same seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Regulatory Affairs Manager
Amgen Europe B.V. · Breda, Netherlands · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Regulatory Affairs
AbbVie · Maidenhead, ENGLAND · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Regulatory Affairs US & Canada Strategy Lead – Therapeutic Neurotoxins - Hybrid
AbbVie · Irvine, CA · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Regulatory Affairs US & Canada Strategy Lead – Therapeutic Neurotoxins - Hybrid
AbbVie · Cambridge, MA · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.