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Principal Consultant - Regulatory Affairs
NNIT A/S —Dublin, County Dublin
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TechBiz Global GmbH —Dublin, County Dublin
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Spanish Point Technologies —Clontarf, County Dublin
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Salesforce —Dublin, County Dublin
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Senior Solutions Architect
HubSpot —Dublin, County Dublin
- €67,200–€97,400 a year
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Construction Engineer – Nightworks
Sacyr —Dublin, County Dublin
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Sacyr —Dublin, County Dublin
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Principal Consultant - Regulatory Affairs

NNIT A/S -
Dublin, County Dublin

Apply Now

Job details

Permanent
13 days ago

Qualifications

French
Spanish
Danish
Sales
English
Master's degree
Business development
Project management
Bachelor's degree
IT
Italian
Communication skills
German
Information Technology

Full job description

8 locations available
|
req1700

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Posted on: 29/06/2026
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Job available in these locations:
Denmark
Follonica GR, Italy
Dublin, Ireland
Saint Asaph, London, United Kingdom
Madrid, Spain
Kraków, Poland
Germany
Basel, Switzerland
Principal Consultant - Regulatory Affairs

Denmark, Germany, Italy, Switzerland, Spain, UK, Ireland, Poland

.nnit-hero__inner { background-image: url('https://mikkeltschentscher.dk/hosting/nnit/assets/images/hero.png'); }
Details
Type of contract: Permanent
Location(s): Denmark, Germany, Italy, Switzerland, Spain, UK, Ireland, Poland
Language(s): English
Mobility: Travel Required
Application Deadline: 31/08/2026

Principal Advisory Consultant - Regulatory Affairs:
NNIT is one of the world’s leading consultancies serving the life sciences industry globally. For more than twenty years, we have enabled our customers to achieve their business goals through digitalization within Quality Assurance, Regulatory Affairs, Clinical, Pharma Production and Laboratory processes.
To further strengthen our Regulatory Affairs team, we are looking for a Principal Advisory Consultant with significant Regulatory Affairs experience and strong expertise within FHIR and healthcare interoperability standards.
You will play a key role in shaping and growing our Regulatory Affairs advisory services with focus on structured data, interoperability, and digital regulatory transformation.

Your responsibilities:
You will join our Regulatory Affairs team as a Principal Advisory Consultant. You will contribute to forming the strategy for growing the Regulatory Affairs business unit with focus on FHIR and structured data, and you will be co responsible for executing this strategy through business development, thought leadership, and client delivery.

On average you will split your time:
60% delivering consultancy projects in advisor, project lead, architect, or engagement delivery lead roles with focus on FHIR enabled regulatory solutions
20% business development, presales, and thought leadership activities within Regulatory Affairs and interoperability
10% development of consultancy offerings, delivery methodologies, and training materials related to FHIR and digital regulatory transformation
5% development and delivery of RFP responses to secure new and expanded client engagements
5% coaching and mentoring consultants across all levels within the Regulatory Affairs team

In your client engagements, you will:
Advise on implementation and governance of FHIR standards in regulatory contexts
Support integration of FHIR with RIM systems, IDMP, and structured content management platforms
Translate global regulatory requirements into compliant, data driven and interoperable solutions
Act as trusted advisor to senior stakeholders in pharmaceutical, biotech, and medtech organizations
Drive alignment between business, regulatory, and IT functions

Your qualifications and experience:
Essential requirements:
Bachelor degree or equivalent in Pharmaceutical Compliance, Regulatory Affairs, Life Sciences, or related discipline
Significant experience in Regulatory Affairs within a pharmaceutical, biotech, or medtech company or as a consultant
Proven consulting experience within a recognized consultancy serving life sciences clients
Strong knowledge of FHIR and its application in healthcare data exchange and regulatory use cases
Experience with global regulatory frameworks including EMA and FDA
Demonstrated experience in sales and business development within a consulting environment
Strong stakeholder management skills and ability to engage clients, partners, and vendors
Excellent documentation, communication, and interpersonal skills in English

Preferred requirements:
Master degree in Pharmaceutical Compliance, Regulatory Affairs, or related field
Experience with RIM systems and IDMP
Knowledge of data governance and Master Data Management principles
Experience bringing new products to market in regulated environments
People management experience and track record of leading complex multi stakeholder projects
Project management experience with consistent on time and on budget delivery
Fluency in an additional European language such as German, Danish, Italian, Spanish, or French

Why join NNIT

A dynamic workplace with strong professional community and focus on collaboration
Opportunity to work with leading life sciences companies across Europe
Influence on strategic direction and growth of our Regulatory Affairs advisory services
Competitive salary, bonus, and benefits package
Clear personal development model supporting your long term career goals
Multicultural environment with an open and professional working culture

We are hiring into our European team in the following countries: UK and Europe – the role can be based in any European country where NNIT has an office location – Denmark, Germany, Ireland, Switzerland, Italy, Spain

Fluency in oral and written English is a must. A second language (Danish, German, Italian, Spanish or French) is desired but not essential.

Travel must be expected, but will be kept to necessary business trips (< 10%).

What’s next?
If you recognize yourself in this role, we’ll be looking forward to hearing from you. Please apply with a full resume and references that describe your abilities with regard of taking this leading role in NNIT’s Lab Consulting team.

and make your mark!

About NNIT

NNIT is a publicly listed company that specializes in IT solutions to life sciences internationally, and to the public and enterprise sectors in Denmark. We focus on high complexity industries and thrive in environments where regulatory demands and complexity are high. We advise on and build sustainable digital solutions that work for the patients, citizens, employees, end users or customers.

NNIT consists of group company NNIT A/S and subsidiaries SCALES, Excellis Health Solutions and SL Controls. Together, these companies employ more than 1,600 people in Europe, Asia, and USA.

We celebrate diversity and are dedicated to fostering an inclusive environment for all employees. We actively work to eliminate bias and ensure an inclusive workplace where everyone has the right to be seen and heard as they are. We invite interested candidates to apply, no matter their background.

In the interest of fostering a fair and unbiased recruitment process, we kindly request candidates to refrain from including their pictures in their applications.

Learn more about working at NNIT
and liberate your talent!

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