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Merck

Merck

Pharma · Pharma

HQ
Rahway, US
Founded
1891
Size
70,000+
Website
merck.com

Currently tracking 14 active AI roles, up 295% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $129k–$203k (avg $166k).

Hiring
14 / 18
Momentum (4w)
↑+567 +295%
759 opens last 4w · 192 prior 4w
Salary range · avg $166k
$129k–$203k
USD · disclosed roles only
Tracked since
6w ago
last role yesterday
Hiring velocityscroll left for older weeks
1 new role
Aug 18
2 new roles
Dec 1
1 new role
8
1 new role
15
1 new role
Jan 5
1 new role
19
2 new roles
26
1 new role
Feb 9
1 new role
16
2 new roles
23
7 new roles
Mar 2
8 new roles
9
9 new roles
16
17 new roles
23
55 new roles
30
45 new roles
Apr 6
75 new roles
13
98 new roles
20
249 new roles
27
319 new roles
May 4
93 new roles
11

Jobs (4)

14 AI · 575 total active
FilteredFunctionEngineering×CountryJapan×Clear all
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Active onlyAI only (≥ 7)
Stage
AllData · 3Pretrain · 1Post-train · 5Agent · 11Eval Gate · 2Ship · 9
Function
AllEngineering · 300Product · 190Research · 85
Country
AllUnited States · 186Netherlands · 43France · 41Czech Republic · 40India · 37China · 29Singapore · 28Germany · 23Japan · 20Ireland · 14United Kingdom · 11United Arab Emirates · 8Vietnam · 8Colombia · 7New Zealand · 7Austria · 6Taiwan · 6Malaysia · 5Mexico · 5Philippines · 4Australia · 3Brazil · 3Canada · 3Costa Rica · 3Latvia · 3Romania · 3Switzerland · 3Argentina · 2Estonia · 2Finland · 2Italy · 2Norway · 2Poland · 2Saudi Arabia · 2Spain · 2Sweden · 2Denmark · 1Hungary · 1Indonesia · 1Israel · 1Lithuania · 1Peru · 1South Africa · 1South Korea · 1Ukraine · 1
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R&D Clinical Quality Assurance Senior Specialist
This role is a Senior Specialist in R&D Clinical Quality Assurance at Merck, focusing on ensuring data integrity and compliance with global regulatory requirements in clinical trials across the APAC region. The primary responsibilities include conducting GCP audits, preparing audit reports, collaborating with various teams to resolve observations, and supporting the overall quality assurance processes within clinical development.
—EngineeringTokyo, Japan6w ago0
R&D Study Operation General & Specialty Medicine/IDs Vaccines Clinical Research Manager
This role is for a Clinical Research Manager at Merck, focusing on leading clinical trial operations in Japan. Responsibilities include managing trial planning, execution, and closure, leading a team, managing costs and risks, and ensuring quality and compliance. The role requires strong English and Japanese language skills, and experience in clinical research management or as a Project Leader at a CRO.
—EngineeringTokyo, Japan6w ago0
R&D Study Operation General & Specialty Medicine/IDs & Vaccines CRM
This role is for an Associate Clinical Research Manager (aCRM) in the General and Specialty Medicine/Infectious Diseases & Vaccines CRM domain at Merck, with a career path towards becoming a Clinical Research Manager (CRM). The aCRM will gain skills and knowledge in clinical trial operations under the guidance of a CRM, potentially also performing CRA duties. The CRM role involves leading clinical trial operations in Japan, collaborating with US counterparts, managing trial teams, vendors, costs, milestones, risks, and supporting site-level issue resolution.
—
Engineering
Tokyo, Japan
6w ago
0
Manufacturing Division Quality Control Associate Director
Associate Director in Quality Control for Merck's Manufacturing Division, responsible for leading a team of quality control laboratory analysts and managing quality testing for raw materials, components, and finished drug products in a pharmaceutical manufacturing setting. Ensures compliance with cGMP, safety, and environmental regulations, manages quality systems, investigations, and corrective actions. Oversees method transfers, safety measures, budget forecasting, and continuous improvement initiatives. Requires a Bachelor's degree in a science/life science field, at least 8 years of experience in pharmaceutical quality operations/control with 3 years of people management, and strong understanding of analytical methodology and regulatory standards.
—EngineeringSaitama, JapanJan 90