Advanced QC professional (Bagsværd, Capital Region of Denmark, DK)

Bagsværd, Denmark Type not listed
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Novo Nordisk 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

Equipment Quality Control Professional

Denmark - Bagsværd

Do you have a passion for working with QC laboratory equipment ? Are you interested in metrology, qualification, and maintenance of analytical equipment, and wish to upgrade our laboratory with automated procedures and tools for the future?

If so, as a maternity cover, you can join us as Equipment Quality Control Professional in Microbiological Quality Control department, located in Bagsværd and Gentofte. Read on to find out more, and apply today and join us for a life changing career!

Your new role

As an Equipment Quality Control Professional in the Equipment Team, you will be responsible for securing compliance and minimising downtime across a diverse portfolio of analytical equipment – from isolators and autoclaves to MALDI-TOF instruments, LAL readers, incubators, balances and temperature monitoring systems.

Your key responsibilities will include:

Providing equipment support to analytical teams, ensuring they can conduct the analyses necessary to release finished products on time

Approving required documentation for both planned and unplanned maintenance of analytical equipment

Setting and maintaining calibration requirements, managing change requests and securing qualification approvals

Performing equipment qualifications (URS, IQ, OQ and PQ) when implementing new equipment

Contributing to ongoing optimisation of existing processes by staying curious about how other teams and departments operate, both inside and outside of Novo Nordisk

Your new department

In Enterprise IT & Quality, you will be part of a business area that drives impact across the full Novo Nordisk value chain. We strive to stay close to our stakeholders in the business to ensure we deliver on their needs, helping reach millions of people living with serious chronic diseases. Our focus is on being at the forefront within our three areas; ensuring the highest quality for patients, being a trusted tech leader and an environmentally responsible business.

QCM RA department of around 65, located in Gentofte and Bagsværd. The department holds overall responsibility for the microbiological analysis of products and water samples from our worldwide production sites – including environmental monitoring, Test for Sterility, Bacterial Endotoxin Testing and Total Viable Count. Daily operations involve close collaboration with other QC laboratories, IT departments, Quality Assurance and external vendors.

Your skills & qualifications

We are looking for a quality-minded professional who thrives in a collaborative environment and takes pride in keeping equipment compliant and available. You will bring:

An MSc degree in Sciences, Engineering, Biotechnology, Pharma or a similar field

Preferably 2+ years of experience with equipment from a QC function in the pharmaceutical industry or other highly regulated industries

Knowledge of criteria for maintaining analytical equipment and GMP equipment qualification

Experience in setting and maintaining calibration criteria and working with metrology is advantageous, as well as change request and technical writing experience

Fluent spoken and written English; Danish is also preferred

As a person, you are self-motivated and never afraid to take initiative or take on responsibility. You are a strong communicator who builds relationships naturally and is known for excellent collaboration skills. You have a systematic approach to problem-solving, a flair for processing data and you are energised by engaging with colleagues and stakeholders.

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

Salary

For this role, the Annual Base Salary ranges from 570,200.00 to 838,100.00 DKK, corresponding to the level of the position.

The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.

Deadline

22nd of September 2026. Applications are reviewed on an ongoing basis.

 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

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Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Bagsværd, 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 1075 comparable Quality roles across 129 biopharma companies.

1075Comparable roles tracked
955Currently active
129Companies hiring similar roles
54Countries represented

Salary context

197 of 1075 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 $570,200/yr – $838,100/yr
Lowest disclosed · Exp Tech Quality Control · Johnson & Johnson $38,500/yr – $61,985/yr
Highest disclosed · Vice President, Quality Assurance - GMP · Exelixis Inc $315,500/yr – $366,500/yr
Peer group range $50,243 – $341,000 (median $151,100)

Where these roles are based

Top locations among the 1075 comparable roles

United States330
Ireland61
Germany55
China55
India51
Japan44

+ 48 more countries

Seniority mix

475 of 1075 peers have a known seniority level

Manager182
Senior130
Associate Director42
Director38
Principal24
Associate23
Senior Director20
Intern/Fellow/Postdoc12
Executive/VP4

Therapeutic area mix

2 of 1075 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease1
Vaccines & Infectious 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.

40%similar
Novo Nordisk Hillerød, Denmark
Same function Same country
40%similar
Novo Nordisk Bagsværd, Denmark Senior Director
Same function Same country
40%similar
H. Lundbeck Copenhagen, Denmark
Same function Same country
40%similar
Novo Nordisk Søborg, Denmark Associate
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.

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.

40%
GMP Professional (Hillerød, Capital Region of Denmark, DK)
Novo Nordisk · Hillerød, Denmark · Seniority not listed
Function Therapeutic area Seniority Country
40%
GCP Advisor Specialist, Clinical QA, Søborg, Denmark (Søborg, Capital Region of Denmark, DK)
Novo Nordisk · Søborg, Denmark · Associate
Function Therapeutic area Seniority Country
25%
Principal Scientist GMP Microbiology Lilly Medicine Foundry
Lilly · Lebanon, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
25%
Senior Manager, Clinical Quality Assurance
AbbVie · North Chicago, IL · 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.