Merck KGaA Posted September 19, 2026

Digital Products Quality Engineering Lead (all genders)

Darmstadt, Hessen, Germany FULL_TIME
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Merck KGaA 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

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

Your role

As Digital Products Quality Engineering Lead, you will shape the quality strategy for digital products developed and maintained in an Agile environment. You will lead and develop a team of software quality engineers, ensuring that digital products meet the quality standards required by customers in regulated life-science environments. Working with global, cross-functional teams, you will champion built-in quality, shift-left practices, and continuous verification throughout the product lifecycle.

You will oversee end-to-end quality assurance and quality control activities, applying the four-eyes principle, managing escalations, and resolving issues with pace and clarity. You will establish and continuously improve software development processes, quality workflows, templates, and key quality indicators. By influencing engineering teams and strengthening their quality mindset, you will help turn complex challenges into practical actions that support faster go-to-market delivery. You will ensure that product engineering artifacts, traceability, testing evidence, and operational controls are inspection-ready and aligned with customer expectations and applicable regulations. Your expertise will help advance risk-based quality management, software test automation, DevOps, and continuous integration and delivery practices.

You hold a bachelor’s or higher degree in Computer Science, an Engineering discipline, Information or Operational Technology, Digital and Data Management, Information Science or Management, Biomedical Science, Life Sciences, or a related field.

You bring at least 10 years of combined experience in software development or engineering, digital transformation, software quality assurance or control, and software quality management, ideally in a life-science or pharmaceutical environment.

You have experience managing or supervising teams and building quality engineering capabilities through coaching, mentoring, and competency development.

You have a strong command of the software product lifecycle, change management, Agile product development, DevOps, Lean, Plan-Do-Check-Act, software test automation, cloud platforms, and risk-based quality management systems; experience with Computer Software Assurance is an advantage.

You understand GAMP 5 supplier-focused principles and relevant software-related ISO standards, as well as quality expectations in regulated environments, including GMP, GCP, GLP, and 21 CFR Part 11 compliance.

You have a proven track record in software operational controls, including change and incident management, audit support, supplier quality, periodic reviews, deviations, and corrective and preventive actions.

You are experienced in design reviews, verification activities, reviewing software engineering artifacts and testing evidence, managing defects, maintaining product traceability, and supporting audits or inspections.

You communicate clearly in writing and verbally, are confident using tools such as Word, Excel, PowerPoint, SharePoint, and project-planning applications, and are willing to travel globally when required.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Darmstadt, Hessen, Germany
Employment type
FULL_TIME

How this role compares

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

We currently track 1008 comparable Quality roles across 131 biopharma companies.

1008Comparable roles tracked
957Currently active
131Companies hiring similar roles
48Countries represented

Salary context

193 of 1008 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 · Quality Control Stability Technician · Regeneron Pharmaceuticals, Inc (USA) $19/hr – $30/hr (≈ $39,395–$61,610/yr)
Highest disclosed · Quality Assurance Specialist · Merck KGaA $65,100/yr – $976,000/yr
Peer group range $50,502 – $520,550 (median $136,700)

Where these roles are based

Top locations among the 1008 comparable roles

United States350
Germany53
Ireland53
China53
Switzerland39
France38

+ 42 more countries

Seniority mix

498 of 1008 peers have a known seniority level

Manager160
Senior116
Intern/Fellow/Postdoc60
Associate Director40
Associate39
Director32
Principal23
Senior Director20
Executive/VP8

Therapeutic area mix

2 of 1008 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1
Respiratory1

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
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40%similar
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Same function Same country
40%similar
Boehringer Ingelheim Ingelheim, Germany Intern/Fellow/Postdoc
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40%similar
Boehringer Ingelheim Ingelheim, Germany Intern/Fellow/Postdoc
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40%similar
Bayer Weimar, Germany Intern/Fellow/Postdoc
Same function Same country

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%
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Sanofi-Aventis Deutschland GmbH · Frankfurt am Main, Germany · Intern/Fellow/Postdoc
Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
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Bayer · Berlin, Germany · Intern/Fellow/Postdoc
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Pharmaziepraktikant*in im Bereich Quality Control
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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.