Orifarm Posted October 16, 2026

Head of Corporate Quality Systems (Odense S, DK, 5260)

Odense S, Denmark Type not listed
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Orifarm 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

Orifarm has launched Fit to Scale, our strategy to grow revenue from €2 billion to more than €3 billion by 2031. We are looking for an experienced quality leader to build a simple, harmonised and scalable Quality Management System that supports our continued growth across Europe

 

About the job

This is an important time to join Orifarm. Our growth ambitions require a strong and scalable quality foundation. One QMS - our common Quality Management System across Orifarm - is therefore a key strategic priority.

As Head of Corporate Quality Systems, you will own Orifarm’s global QMS and lead the One QMS transformation. Working closely with Quality Heads, operational sites, sales countries, Corporate IT and business leaders, you will ensure that common quality processes are practical, effective and consistently applied across the organisation.

Your key responsibilities will include:

Define the global QMS strategy and roadmap and lead the transition to One QMS

Harmonise and simplify quality processes across functions, countries and operational sites

Build strong partnerships with Quality Heads and local leaders to agree, implement and sustain common standards

Govern and maintain the global QMS, including quality policies, procedures and the electronic Quality Management System

Act as process owner for corporate quality processes and ensure continued compliance and inspection readiness

Drive continuous improvement and digitalisation, including the appropriate use of AI to simplify quality processes

Own the global quality KPI framework and lead the Management Review process, providing senior management with clear insight into quality performance, risks and improvement priorities

Lead the global Quality Culture programme and promote a proactive, patient-focused quality mindset

You will report to the VP, Quality Management and lead a team of Senior QMS Specialists. The position is based in Odense, Denmark, with a hybrid working model requiring three days per week on site.

 

Who are you?

You bring at least ten years of experience in pharmaceutical quality management or another highly regulated industry, such as biotechnology, medical devices or healthcare. You hold a bachelor’s or master’s degree in pharmacy, life sciences, engineering, chemistry or a related discipline.

You have extensive experience with global Quality Management Systems and a proven track record of leading quality transformation and harmonisation in a global matrix organisation. You understand relevant GxP requirements and have supported regulatory inspections and audits. Experience with electronic quality systems is essential.

You bring a strong LEAN and continuous-improvement mindset and can identify opportunities to make quality processes simpler, more effective and digitally enabled, including through the appropriate use of AI.

As a leader, you build trust, create commitment and work effectively across functions, countries and sites. You combine strategic and risk-based thinking with the ability to challenge constructively. You are comfortable engaging with senior leaders and regulatory inspectors and bring the integrity, resilience and drive required to lead a significant transformation.

You are fluent in written and spoken English. Additional languages are an advantage.

 

Who are we?

Corporate Quality Systems is part of Quality Management within Orifarm Operations. Our team of Senior QMS Specialists works cross-functionally with Quality teams across Orifarm, Corporate IT, Regulatory Affairs, Global Safety & business leaders. English is our corporate language.

The team provides the framework for how quality systems are governed across Orifarm. Through One QMS, you and the team will help make Orifarm fit to scale while supporting our purpose of improving access to affordable, high-quality medicines across Europe.

 

Why should you join Orifarm?

At Orifarm, we are 2,300 employees united by a shared purpose: improving access to affordable medicine for the people who need it. Founded in Odense, Denmark in 1994 by Birgitte & Hans Bøgh-Sørensen, we have built our business on challenging conventional thinking to make affordable high-quality pharmaceuticals more accessible across Europe. Rather than developing new medicines, we focus on finding smarter ways to bring existing treatments to patients, creating value for pharmacies, healthcare systems, and society.

We live by the mindset Challenge Accepted . It reflects our explorer spirit and can-do attitude, where challenges are perceived as opportunities. We encourage people to ask questions, challenge assumptions, and take ownership. Across teams, functions, and markets, you will find a collaborative and supportive culture built on trust, respect, and a flat hierarchy where everyone has a voice and direct access to decision-makers.

When you join Orifarm, you will be empowered to make a real impact from day one. We offer autonomy and great opportunities for career advancement, enabling our employees to shape their professional development. We value flexibility and provide a hybrid work model with the possibility of working from home two days a week.

We invite you to join Orifarm, if you are curious, ambitious, and accept the challenge of bringing better deals of medicine to millions.

We encourage everyone to apply

At Orifarm, we welcome people from all backgrounds, recognizing that the best outcomes come from a diverse and inclusive work environment. Our commitment is to create an environment where different perspectives and skills drive innovation and contribute to a sustainable future. By creating such an environment, we are confident that we can achieve better results together.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Odense S, Denmark
Employment type
Not listed

How this role compares

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

We currently track 1524 comparable Quality roles across 146 biopharma companies.

1524Comparable roles tracked
1326Currently active
146Companies hiring similar roles
53Countries represented

Salary context

261 of 1524 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · QC Lab Technician (Lilly Contractor - Fixed Term) · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $43,753 – $350,000 (median $122,900)

Where these roles are based

Top locations among the 1524 comparable roles

United States617
Ireland90
France75
Germany70
China68
India61

+ 47 more countries

Seniority mix

741 of 1524 peers have a known seniority level

Manager222
Senior178
Intern/Fellow/Postdoc104
Associate71
Associate Director51
Director45
Principal38
Senior Director25
Executive/VP7

Therapeutic area mix

2 of 1524 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease2

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.

40%similar
Novo Nordisk Kalundborg, Denmark
Same function Same country
40%similar
Novo Nordisk Søborg, Denmark
Same function Same country
40%similar
Novo Nordisk Kalundborg, Denmark
Same function Same country
25%similar
Lilly Lebanon, Indiana, United States of America Principal
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie North Chicago, IL Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

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.

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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.

40%
Quality Assurance Professional (Kalundborg, Region Zealand, DK)
Novo Nordisk · Kalundborg, Denmark · Seniority not listed
Function Therapeutic area Seniority Country
25%
Principal Scientist GMP Environmental Monitoring Lilly Medicine Foundry
Lilly · Lebanon, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
25%
Sr R&D Quality Assurance Engineer F/M
AbbVie · Annecy, Auvergne-Rhône-Alpes · Senior
Function Therapeutic area Seniority Country
25%
QA Specialist III
Gilead Sciences, Inc. · La Verne, United States · Seniority not listed
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.