Merck KGaA Posted October 20, 2026

Material Handler 2

Rockville, Maryland, 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 EMD Serono.

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.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

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

Your Role:

The Material Handler 2 will execute receiving, inspection, storage, distribution and/or shipment of materials and/or samples in a GMP regulated environment.  This role executes core tasks with minimal supervision and guidance. The Material Handler 2 ensures materials and/or samples are received, stored, distributed and/or shipped to support Testing Operations within BioReliance and our clients.  Specific responsibilities include:

Receive materials, client samples and/or internal finished goods daily. Check and process received items in line with appropriate quality procedures (physical / quantity check and paperwork verification). ​

Ensure inventory is stored and distributed in line with agreed quality / regulatory compliance (e.g. GMP material control, temperature control) and provide traceability through maintenance of accurate system transactions (ERP or LIMS).  ​

Maintain stock accuracy at all times through timely system maintenance such as cycle counting and routine disposal. ​

Actively maintains a clean, audit ready and safe work environment including equipment monitoring/maintenance under the responsibility of the department ​.

Perform inter-site transfer of samples or materials between departments. May be completed via internal transportation or courier. ​

Operate material handling equipment as necessary (e.g. hand truck, pallet jack, dock lever, etc.) ​

Notifies relevant personnel immediately and escalate to Supervisor/Manager should a deviation or other unexpected observation occur. ​

Communicate and interact professionally with all levels of the organization. This includes timely communications and responses via business applications. ​

Perform tasks in accordance with SOPs and regulations (e.g. cGMP and GLP) and complies with company Quality and EHS regulations and procedures.   ​

Supports and/or leads small department continuous improvement or business projects as agreed by line management with a view to streamlining processes, making cost savings or reducing waste.

Supports deviation investigations and implementation of corrective actions and can open related Quality Management System records.

Maintains all records and archives as appropriate following the appropriate Standard Operating Procedures (SOPs).

Supports Internal/Client/Regulatory audit tours.

Mentors others in relevant Supply Chain processes

Pick, pack and ship (domestic/international) materials in line with client requirements and in accordance with relevant shipping SOP documentation and regulations.

Communicates with Customer & Client Support Managers, Labs, PM and other BioReliance sites regarding outgoing shipments.

Troubleshoots courier and/or delivery issues.

Who You Are

Minimum Qualifications:

HS Diploma or GED with 3+ years of experience in a logistics or warehouse role

OR ​

Associates degree in any discipline with 1+ years of experience in a logistics or warehouse role

Preferred Qualifications:

Domestic and international shipping experience.

Prior experience in a Life Science or Biotechnology role.

Working knowledge of basic computer systems (MS Word, Excel, Outlook) and databases such as Oracle ERP or LIMS.

Excellent oral and written communication skills.

Comfortable working in PPE as required (lab coat, safety glasses, gloves, safety shoes, etc.)

Dangerous Goods shipping certification or ability to pass certification process.

Pay Range for this position: $21-$33/hour

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
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Rockville, Maryland, 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 3720 comparable Manufacturing & CMC roles across 172 biopharma companies.

3720Comparable roles tracked
3319Currently active
172Companies hiring similar roles
64Countries represented

Salary context

905 of 3720 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 $21/hr – $33/hr (≈ $43,680–$68,640/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $0 – $381,150 (median $127,600)

Where these roles are based

Top locations among the 3720 comparable roles

United States1723
Germany246
India162
France148
Ireland133
China121

+ 58 more countries

Seniority mix

1647 of 3720 peers have a known seniority level

Senior429
Manager374
Intern/Fellow/Postdoc251
Associate165
Principal134
Director118
Associate Director114
Senior Director53
Executive/VP9

Therapeutic area mix

24 of 3720 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease15
Rare Disease3
Oncology3
Respiratory1
Dermatology & Aesthetics1
Immunology1

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
AstraZeneca New Haven, Connecticut, United States of America
Same function Same country
40%similar
40%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Intern/Fellow/Postdoc
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Director
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.

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.

40%
Development Scientist III, Analytical Development and Clinical Quality Control
AstraZeneca · New Haven, Connecticut, United States of America · Seniority not listed
Function Therapeutic area Seniority Country
40%
Director - Analytical Chemistry
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Director, Global Regulatory Affairs - Chemistry, Manufacturing and Controls (CMC), Platform Innovation - Small Molecules
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Principal Scientist/Engineer, Drug/Device Combination Products - Device Characterization
Merck · Rahway, New Jersey, United States of America · Principal
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.