Novo Nordisk Posted October 24, 2026

Director of Quality Control (Montes Claros - MG) (Montes Claros, Minas Gerais, BR)

Montes Claros, Brazil Type not listed
Quality Director
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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

Your impact begins here

As Director, Head of Quality Control, you will take overall responsibility for Quality Control at the Montes Claros site and lead approximately 80 colleagues. You will set the direction for the function, keep laboratory operations reliable and make sure QC meets applicable quality requirements while supporting manufacturing and supply. Your leadership will help ensure that the medicines people depend on are backed by quality that can be trusted.

What you’ll bring

Substantial experience in pharmaceutical quality control and a strong understanding of GMP in a manufacturing environment.

A relevant degree in a scientific discipline.

A proven record of leading a large technical organisation, including developing leaders and building effective teams.

Sound quality judgement, with the ability to set priorities and improve performance.

The ability to work across functions and cultures.

Fluent English, written and spoken, to work with global stakeholders.

Useful, but not essential:

Experience collaborating with both site leadership and global stakeholders.

Fluent Portuguese.

What you’ll do

You will lead QC at a major manufacturing site, making sure the function is ready for today’s demands and for how the site is evolving.

Set the direction for QC, and lead, coach and develop an organisation of approximately 80 colleagues.

Ensure QC activities are planned, performed and documented in line with applicable GMP requirements and approved procedures.

Oversee laboratory capacity, performance and priorities to support manufacturing, supply and evolving site needs.

Provide leadership for the investigation of laboratory deviations and out-of-specification results, and for effective corrective and preventive actions within QC.

Maintain inspection readiness and represent QC in audits and regulatory inspections.

Build a culture of quality, accountability, safety and continuous improvement across the QC organisation.

Who you’ll work with

You will be based at the Montes Claros site in Brazil and report to the Senior Director, Global QC IO, with a dotted reporting line to the Head of QA at the site. Your QC team of approximately 80 colleagues will look to you for clear direction and priorities.

Your closest partners will be QA, Production and other site functions. You will align local QC strategy and priorities with Global QC IO, so decisions are made with clarity and the work keeps moving. In Global Manufacturing & Supply, colleagues work across the value chain to scale molecules, processes, devices and products for the people who need them.

What you can expect here

You will lead with the trust of site and global colleagues, and be supported to perform at your best. The role gives you room to shape how QC contributes to the Montes Claros site, to develop leaders in your organisation, and to grow your own perspective by working with both site leadership and global stakeholders.

We value clear priorities, honest feedback and decisive action. You will be part of a team that holds quality and safety to a high standard while staying focused on results.

Start now

Your impact begins today. If you are ready to lead QC at Montes Claros and take responsibility for quality at a major manufacturing site, apply for the Director, Head of Quality Control role by 1 November 2026. Applications are reviewed on an ongoing basis, so we encourage you to apply as soon as possible.

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Job details

Seniority
Director
Function
Quality
Therapeutic area
Not listed
Location
Montes Claros, Brazil
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 102 comparable Director Quality roles across 34 biopharma companies.

102Comparable roles tracked
90Currently active
34Companies hiring similar roles
18Countries represented

Salary context

46 of 102 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 · Senior / Principal Associate QA API External Manufacturing · Lilly $65,250/yr – $169,400/yr
Peer group range $117,325 – $285,000 (median $214,088)

Where these roles are based

Top locations among the 102 comparable roles

United States63
Switzerland7
Belgium5
Japan3
Germany3
Ireland3

+ 12 more countries

Seniority mix

102 of 102 peers have a known seniority level

Principal37
Director35
Senior Director30

Therapeutic area mix

0 of 102 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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.

45%similar
AbbVie North Chicago, IL Director
Same function Same seniority
45%similar
Mylan Teoranta Inverin, Ireland Director
Same function Same seniority
45%similar
Gilead Sciences, Inc. Foster City, United States Director
Same function Same seniority
45%similar
AstraZeneca Hamilton, Ontario, Canada Director
Same function Same seniority
45%similar
Gilead Sciences, Inc. Foster City, United States Director
Same function Same seniority
45%similar
Johnson & Johnson Chiyoda, Japan Director
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.

Or follow a whole field: get every new Quality job in Brazil, and choose locations and companies.

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.

45%
Director, Clinical Quality Assurance
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
45%
Site Quality Director
AstraZeneca · Hamilton, Ontario, Canada · Director
Function Therapeutic area Seniority Country
45%
Director Quality Control
Teva Pharmaceuticals · Kfar Saba, Israel · Director
Function Therapeutic area Seniority Country
45%
Director QA Protein Modality (Berlin, BE, DE, 10179)
BioNTech · Berlin, Belgium · Director
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.