Merck KGaA Posted October 13, 2026

Sr. Validation Engineer

Indianapolis, Indiana, United States 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!  Start your next chapter and join MilliporeSigma.

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.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

Validation is the backbone of pharmaceutical manufacturing quality, and in this role, you will own it.​ As a Sr. Validation Engineer, you will lead and execute validation activities across a complex aseptic manufacturing site, with a primary focus on the cleaning validation program. You will research, author, coordinate, and execute validation protocols covering process, equipment, facility, utilities, computerized systems, and cleaning. Working with considerable autonomy, you will review and summarize data for management approval, perform revalidations, assess the impact of change control requests, and create and update standard operating procedures. You will also serve as validation lead on cross-functional projects, develop validation master plans, and support media fills. Your technical depth and independent judgment will directly protect product quality and regulatory compliance.

Who You Are

Minimum Qualifications:

B.S. in science or engineering related field and 7 years validation experience or equivalent combination of two-year degree and a minimum of 9 years validation experience in an aseptic pharmaceutical setting focused on equipment cleaning (automated and manual).

Experience with aseptic bulk process formulation, aseptic filling, process and packaging equipment, computer systems, process control systems, equipment cleaning and sterility assurance required.

 

Preferred Qualifications:

Experience with various types of validation test equipment, such as: Kaye Validator, Val Probe, PLC, Temperature/Pressure standards.

Prior experience (required) in the qualification of various types of sterile filling facility equipment, such as:

o Sterilization Technology (Steam, Dry Heat, VHP, etc.)

o Temperature Mapping (Various chambers)

o Aseptic Equipment (Washers, Tunnels, Cappers, RABS, Isolators etc.)

o Pharmaceutical Grade Utilities

o Process Validation

o Cleaning Validation

Hands-on skills are necessary.

Expertise with Windows based Personal Computers.

Above average PC skills with spreadsheets, word processing and databases.

Employee must be self-motivated, highly organized, and conscientious.

Must be able to work and make decisions independently as well as with a team.

Must be able to work in technically and mentally demanding situations.

Strong verbal and written communications skills are required.

This role requires regular access to process areas by climbing stairs and ladders and performing work in those areas.

Employee must be available to work various shifts and weekends to support the Validation Schedule.

Proficiency with statistical analysis tools and the ability to interpret and present complex data sets.

Pay Range for this position: $111,200 - $166,800

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here .

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
Senior
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Indianapolis, Indiana, United States
Employment type
FULL_TIME

How this role compares

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

We currently track 676 comparable Senior Manufacturing & CMC roles across 84 biopharma companies.

676Comparable roles tracked
611Currently active
84Companies hiring similar roles
36Countries represented

Salary context

262 of 676 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 $111,200/yr – $166,800/yr
Lowest disclosed · Senior Technician Calibration - Maintenance · Mylan Technologies, Inc. $37,000/yr – $80,000/yr
Highest disclosed · Principal Scientist, Oral Formulation Sciences · Merck $173,200/yr – $272,600/yr
Peer group range $58,500 – $222,900 (median $151,700)

Where these roles are based

Top locations among the 676 comparable roles

United States450
India35
Ireland28
Netherlands24
United Kingdom15
Switzerland11

+ 30 more countries

Seniority mix

676 of 676 peers have a known seniority level

Senior428
Principal134
Associate Director114

Therapeutic area mix

6 of 676 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease3
Oncology2
Dermatology & Aesthetics1

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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.

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60%similar
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Same function Same seniority 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.

Or follow a whole field: get every new Manufacturing & CMC job in the United States, 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.

60%
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Function Therapeutic area Seniority Country
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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.