Full-Time

Quality Assurance Manager

Posted on 9/10/2026

Deadline 9/25/26
Merck

Merck

10,001+ employees

Pharmaceutical company developing medicines and vaccines

Compensation Overview

$96.2k - $151.4k/yr

+ Annual bonus + Long-term incentive

No H1B Sponsorship

Irving, TX, USA

In Person

No relocation support is provided. Travel is required approximately 10%.

Bachelor's

Category
Manufacturing Quality & Test (1)
Required Skills
Power BI
ERP
SAP Products
Word/Pages/Docs
Quality Assurance (QA)
Excel/Numbers/Sheets
PowerPoint/Keynote/Slides

Get referred to Merck

See people who can refer or advise you

Requirements
  • A Bachelor of Science degree in Mechanical Engineering or Industrial Engineering is preferred; equivalent work experience may be considered.
  • At least five years of quality engineering experience in a manufacturing environment is preferred.
  • Strong written and verbal communication skills are required.
  • Strong supervisory and leadership skills, including experience leading a team, are required.
  • Experience with SAP Enterprise Resource Planning systems is required.
  • Ability to manage changing workloads and complete tasks independently is required.
  • Demonstrated analytical problem-solving and decision-making ability, including a logical approach and the ability to act despite obstacles or ambiguity, is required.
  • Ability to understand technical specifications and requirements is required.
  • High proficiency in Excel, Word, and PowerPoint is required; familiarity with Power BI and Access is an advantage.
  • Solid understanding of quality tools, including statistical process control, Pareto charts, 8D problem solving, Failure Mode and Effects Analysis, Gage Repeatability and Reproducibility, First Article Inspection, process capability index, and Production Part Approval Process, is required.
  • Ability to lead and facilitate training and continuous improvement initiatives is required.
  • Ability to work with all levels of business customers in a highly dynamic environment is required.
  • Ability to work closely across various teams, including functional and procurement leadership teams, is required.
  • Willingness and ability to work flexible hours is required.
Responsibilities
  • Support implementation of all quality processes and coordinate quality activities for the assigned manufacturing unit.
  • Analyze quality data and make recommendations for improvement focus areas.
  • Develop and implement improvements through Kaizen events.
  • Work closely with Engineering to influence technical design decisions, meet custom product requirements, and achieve business objectives.
  • Implement containment and corrective actions, follow up on quality issues, facilitate responses to findings, and handle quality case documentation.
  • Lead problem-solving activities to investigate nonconformities.
  • Serve as the Quality liaison with support groups and cross-functional teams.
  • Coordinate Quality training.
  • Serve as the primary liaison for supplier quality activities.
  • Write, review, and approve Standard Operating Procedures, Controlled Job Aids, Control Procedures, Quality Standards, and related quality documents.
  • Promote company strategic, departmental operational excellence, and manufacturing regulatory initiatives.
  • Act as the quality representative on capital projects.
  • Provide engineering and technical support for current products and new product launches.
  • Interface with customer quality representatives regarding quality problems and ensure effective corrective action is implemented.
  • Interpret customer specifications and requirements.
  • Maintain strong internal and external supplier quality levels.
  • Design and implement methods for process improvement, testing, and inspection.
  • Develop and analyze quality metrics and initiate change as needed.
Desired Qualifications
  • A Bachelor of Science degree in Mechanical Engineering or Industrial Engineering is preferred.
  • At least five years of quality engineering experience in a manufacturing environment is preferred.
  • Familiarity with Power BI and Access is preferred.

Merck is a global healthcare company that develops medicines, vaccines, and animal health products. It advances long-term health by conducting research and development to create new treatments for diseases such as cardiovascular disease, diabetes, and cancer, then brings these medicines to patients, healthcare professionals, and institutions worldwide. The company’s products work by undergoing scientific discovery, clinical testing, and regulatory approval before being manufactured and sold or distributed through patient assistance programs. What sets Merck apart is its large, diversified portfolio across human medicines, vaccines, and animal health, along with a strong emphasis on R&D, global reach, and support services like Merck Connect and Merck Manuals that provide professional resources. Merck’s goal is to tackle major health threats by applying science to discover and deliver therapies that improve patient outcomes and public health across the globe.

Company Size

10,001+

Company Stage

IPO

Headquarters

Kenilworth, Illinois

Founded

1891

Get referred to Merck

See people who can refer or advise you

Simplify Jobs

Simplify's Take

What believers are saying

  • August 2026 melanoma data validated Merck's next-generation cancer franchise beyond Keytruda.
  • July 2026 Lipfendra approval opens a new cardiovascular growth market before Keytruda erosion.
  • February 2026 oncology reorganization concentrates resources ahead of patent expiry and late-stage launches.

What critics are saying

  • Keytruda loses U.S. compound patent protection in December 2028, pressuring oncology revenue.
  • Summit and Akeso's ivonescimab beat Keytruda in China lung cancer data in 2026.
  • Merck's 2025 $3 billion cost-cutting plan includes 6,000 layoffs, signaling margin strain.

What makes Merck unique

  • Keytruda remains Merck's oncology engine; July 2026 approvals expanded perioperative bladder and kidney use.
  • August 2026 Moderna partnership produced first positive Phase 3 individualized mRNA cancer vaccine results.
  • Lipfendra's July 2026 FDA approval created Merck's first oral PCSK9 inhibitor.

Help us improve and share your feedback! Did you find this helpful?

Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

401(k) Company Match

Paid Vacation

Paid Sick Leave

Hybrid Work Options

Growth & Insights and Company News

Headcount

6 month growth

-20%

1 year growth

-20%

2 year growth

-20%
Yahoo Finance
Sep 8th, 2026
Merck cuts 54 jobs in New Jersey as part of $3B cost-reduction plan

Merck & Co. will lay off 54 workers at its Rahway, New Jersey facility in two phases on 11 December 2026 and 4 January 2027, according to a September filing with the state Department of Labor. The cuts are part of a company-wide initiative announced in 2025 to reduce costs by $3 billion by 2027. The pharmaceutical company said savings from the cost-cutting measures would support new products. This follows a previous notice filed in June covering 88 employees, with layoffs scheduled for 4 September. The company has not disclosed the total number of job cuts planned under the initiative.

World Today News
Sep 8th, 2026
Tempus AI raises $600M to scale AI-enhanced liquid biopsy platform for cancer recurrence detection

Tempus AI has raised $600 million in Series C funding to scale its machine learning platform for cancer recurrence detection through liquid biopsies. The investment was led by SoftBank Vision Fund 2, with participation from Roche and Merck. Phase II trial data showed the AI-enhanced liquid biopsy analysis reduced false-negative results by 37% compared to conventional methods. The platform uses deep learning algorithms trained on over 12,000 genomic profiles to identify circulating tumour DNA fragments shed by residual cancer cells. A 2025 Nature Medicine study reported the system achieved 92% specificity in detecting minimal residual disease across breast, lung, and colorectal cancers. According to SEC filings, 45% of funds will support FDA pre-market approval trials, whilst 30% will fund global expansion into EU and APAC markets.

Latest Nigerian News
Sep 5th, 2026
Merck, Cond Nast and Cargill all recently appointed female cfos.

Merck, Cond Nast and Cargill all recently appointed female cfos. Published by Forbes on Fri, 02 Apr 2021 March was a great month for women in finance. Last week, pharmaceutical giant Merck tapped Caroline Litchfield as its new CFO, while media company Cond Nast named Jackie Marks to lead its finance function. Earlier in the month, food corporation Cargill announced Jamie Miller as finance chief.

BioSpace
Sep 3rd, 2026
Summit, Akeso's ivonescimab bests Merck's Keytruda in China trial - again.

Summit, Akeso's ivonescimab bests Merck's Keytruda in China trial - again. September 3, 2026 | New Phase 3 data show that Summit Therapeutics and Akeso's PD-1/VEGF therapy improved overall survival in patients with a type of lung cancer as compared to Merck's Keytruda but the results will need to be replicated in non-Chinese patients. Summit Therapeutics and Akeso's upcoming PD-1/VEGF bispecific antibody has officially bested Merck's mega-blockbuster Keytruda on both overall survival and progression free survival in a type of non-small cell lung cancer. The latest results for the partners could establish a new paradigm in NSCLC treatment where ivonescimab becomes the regimen of choice among oncologists, analysts said. But the new data from the Phase 3 HARMONi-2 trial comes from Chinese clinical trials. Summit still has to verify the results in Western patients to get the FDA on board for a clean regulatory review. Akeso on Thursday announced interim results from the Phase 3 HARMONi-2 trial, which compared ivonescimab against Keytruda in patients with first-line NSCLC with tumors that express PD-L1. The drug is already approved in China for this type of cancer, as well as two others, but has yet to be cleared in the U.S. for any indication. Ivonescimab met the key secondary goal of improving overall survival (OS). The companies previously announced the achievement of the main progression-free survival (PFS) endpoint in May 2024, earning the antibody the nickname Keytruda killer. The therapy achieved PFS of 11.14 months as compared to Keytruda's 5.82 months. Summit Therapeutics planned an early interim progression-free survival readout for HARMONi-3 in the hope of enabling earlier regulatory engagement - but the early analysis delivered disappointment for the company and shareholders. May 4, 2026 "Akeso's HARMONi-2 study has now demonstrated both PFS and OS superiority versus Keytruda in China, raising the possibility that future NSCLC regimens may increasingly be judged against ivonescimab rather than Keytruda," Jefferies wrote in a Thursday morning note. "While investors can reasonably debate whether China data will fully translate globally," the analysts continued, "this latest OS readout strengthens the case for ivonescimab as a potential next-generation immunotherapy backbone in NSCLC." Summit's shares rose over 7% to $15.65 in early morning trading Thursday. Akeso did not reveal detailed data on the OS endpoint but promised to do so at a future medical meeting and in a peer-reviewed journal. In the meantime, Summit is working on confirming these achievements in trials conducted elsewhere. A key test will be the outcome of the global Phase 3 HARMONi-3 trial, which is testing ivonescimab with chemotherapy against Keytruda in patients with first-line metastatic NSCLC. After the drug was approved for this indication in China, the regulator there released additional data on the label that suggested a degradation of the PFS benefit. Analysts raised concerns that the HARMONi-3 trial may not show a sufficient benefit to warrant an accelerated approval from the FDA. Summit is expected to reveal data from HARMONi-3 sometime this half. In May, an early interim analysis of PFS from HARMONI-3 failed to reach statistical significance, postponing Summit's plans for a regulatory filing in this indication. Summit is, however, currently awaiting a November FDA decision for the therapy in NSCLC with mutations in the gene for epidermal growth factor receptor (EGFR). Analysts, investors and partner Summit Therapeutics had all been keenly awaiting the overall survival update, after previous data from Akeso's HARMONi-6 trial left them wanting. May 31, 2026

DIGITIMES
Sep 3rd, 2026
Electroninks, Merck, Qualipoly build advanced packaging ecosystem.

Electroninks, Merck, Qualipoly build advanced packaging ecosystem. Sep 4, 2026, 07:53 0 Credit: DIGITIMES Electroninks, a global provider of metal-composite conductive inks and advanced semiconductor packaging materials, has formed a strategic partnership with Merck and Taiwan-based Qualipoly Chemical to offer advanced packaging customers a more complete, faster,... Picks for you