Top 62 Eisai Jobs | SimplyHired

Mgr., Product Complaints (Hybrid)
Eisai —Raleigh, NC
- $104,900 - $137,700 a year
- Full-time
- Hybrid work
- 5 years
- Engineering
- Neurology
Associate Director, Government Contracts
Eisai —Nutley, NJ
- $161,500 - $212,000 a year
- Full-time
- Hybrid work
- Office
- Master's degree
- 8 years
QA Specialist (Hybrid)
Eisai —Raleigh, NC
- $66,200 - $86,800 a year
- Full-time
- Hybrid work
- Mid-level
- Bachelor's degree
- Continuous improvement
Manager, Product Training - Oncology
Eisai —Nutley, NJ
- $119,100 - $156,300 a year
- Full-time
- 5 years
- Mid-level
- Master's degree
Sr. Manager HRIS - WorkDay
Eisai —Nutley, NJ
- $137,100 - $180,000 a year
- Full-time
- Hybrid work
- Writing skills
- Bachelor's degree
- Continuous improvement
Senior Manager, Data Management
Eisai —Nutley, NJ
- $134,800 - $176,900 a year
- Full-time
- Hybrid work
- 7 years
- Office
- Bachelor's degree
Leader, Field and Sales Training, Alzheimer’s Disease
Eisai —Nutley, NJ
- $201,800 - $264,800 a year
- Full-time
- Sales
- Master's degree
- Supervising experience
Director, Translational Science (Neurology)
Eisai —Nutley, NJ
- $204,300 - $268,200 a year
- Full-time
- Hybrid work
- Medicine
- 8 years
- Doctor of Philosophy
Manager, Medical Information, Oncology
Eisai —Nutley, NJ
- $121,800 - $159,800 a year
- Full-time
- Hybrid work
- Office
- 3 years
- Travel
Administrative Coordinator, Exton Facilities (Onsite)
Eisai —Exton, PA
- $30 - $39 an hour
- Full-time
- Microsoft Outlook
- Word processing
- Mid-level
Associate Director or Director, Medical Science Liaison, Oncology - Central region / Field-based
Eisai —Nashville, TN
- $206,600 - $294,735 a year
- Full-time
- Medicine
- HIPAA
- 8 years
Associate Director, Translational Science (Neurology)
Eisai —Nutley, NJ
- $168,200 - $220,700 a year
- Full-time
- Hybrid work
- 5 years
- Doctor of Philosophy
- Neurology
Global Medical Director, Sleep Disorders - Neurology Global Medical Affairs
Eisai —Nutley, NJ
- $217,000 - $284,800 a year
- Full-time
- Remote
- 5 years
- Bachelor's degree
- Doctor of Philosophy
Senior Manager, Business Excellence & Asset Management
Eisai —Nutley, NJ
- $118,100 - $155,000 a year
- Full-time
- Hybrid work
- Office
- 8 years
- Neurology
Director, Organization Development & Learning
Eisai —Nutley, NJ
- $196,200 - $257,500 a year
- Full-time
- Hybrid work
- Office
- Master's degree
- Psychology
- Work from home
Senior Manager, Medical Information, Oncology
Eisai —Nutley, NJ
- $133,400 - $175,100 a year
- Full-time
- Hybrid work
- Management
- Office
- 8 years
Medical Science Liaison (MSL or Sr. MSL), Neurology (Alzheimer's Disease) - Field Based, Central Midwest (KS, NE, IA & MO)
Eisai —Nutley, NJ
- $144,300 - $216,900 a year
- Weekends as needed
- Clean driving record
- Medicine
- Word processing
Medical Science Liaison (MSL) / Senior Medical Science Liaison (Sr. MSL), Oncology - Texas; Field-based
Eisai —Nutley, NJ
- $144,300 - $216,900 a year
- Weekends as needed
- Medicine
- Word processing
- Office
Medical Science Liaison, (MSL or Sr. MSL) Neurology (Alzheimer's Disease) - Field Based IL and St. Louis, MO
Eisai —Nutley, NJ
- $144,300 - $216,900 a year
- Weekends as needed
- Clean driving record
- Medicine
- Word processing
Associate Director, Discovery IT Portfolio Lead
Eisai —Cambridge, MA
- $166,800 - $218,900 a year
- Full-time
- Hybrid work
- Writing skills
- Engineering
- 8 years

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Mgr., Product Complaints (Hybrid)

Eisai -
Raleigh, NC

Apply Now

Job Details

Full-time
$104,900 - $137,700 a year

Qualifications

Content creation for technical audiences
Technical documentation
Technical writing experience within manufacturing
Quality risk management
Design usability
Biomedical regulatory compliance
Cross-functional collaboration
ISO 13485
Cross-functional communication
FDA regulations

Full Job Description

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.

The Manager, Product Complaints is responsible for the oversight, governance, and continuous improvement of Eisai’s medical device complaint handling process. This role ensures that medical device complaints are consistently captured, appropriately triaged, thoroughly reviewed, and closed in compliance with FDA QMSR (21 CFR Part 820), ISO 13485, EU MDR, and Eisai quality system requirements.
The role serves as the single point of entry for all Raleigh site commercial product complaints to ensure data quality and consistency; however, the position only triages and fully manages medical device complaints. This role is accountable for reviewing, challenging, accepting, and approving investigations from the device manufacturer on behalf of Eisai.
This role partners closely with medical information by providing high-quality medical device complaint data, accepted investigation outcomes, and trend analyses to support vigilance and signal management activities as part of the Post-Market Surveillance program (PMS).

Essential Functions:

Serve as the single point of entry for all Raleigh site product complaints, ensuring timely, accurate, and complete complaint documentation while following established Eisai procedures for routing all complaints.
Triage and classify medical device complaints, including confirmation of device involvement, user error considerations, and potential quality or safety impact.
Own and oversee the end-to-end lifecycle of medical device complaints, including intake, triage, investigation oversight, escalation, documentation, and closure. Apply human factors and usability engineering principles to assess whether events are attributable to user error, use related risk, foreseeable misuse, or product quality/design issues.
Manage complaint sample handling (shipping, tracking) to external sites for investigation.
Review investigation strategies, failure analysis methodologies, root cause determinations, and supporting evidence to ensure investigation adequacy, scientific rigor, and regulatory compliance.
Escalate inadequate, delayed, or non‑compliant investigations through Quality governance and supplier oversight mechanisms.
Establish and monitor medical device complaint metrics, dashboards, and trend analyses (e.g., failure mode, component, lot/batch, time to event).
Ensure complaint data effectively informs CAPA, risk management, and product improvement initiatives.
Author, own, and maintain SOPs related to Complaint Handling and Oversight
Drive continuous improvement initiatives related to complaint handling effectiveness, investigation quality, and compliance.

Requirements:

Bachelor’s or Master’s degree in Engineering, Life Sciences, Quality, Regulatory Affairs, Pharmacy, or a related technical field.
5+ years of experience in medical device complaint handling, post market quality, or related quality system roles, required.
Medical Device (auto-injector) and combination product experience required.
Experience providing oversight of externally performed medical device investigations (e.g., CMOs or device manufacturers) preferred.
Hands‑on experience with complaint systems compliant with 21 CFR Part 820 (QMSR), ISO 13485, and EU MDR.
Prior involvement in medical device recalls or field actions preferred.
Strong knowledge of:
- FDA Medical Device Reporting (21 CFR Part 803)
- EU MDR vigilance and complaint handling requirements
- ISO 14971 risk management principles
- IEC 62366‑1 usability engineering

Strong cross functional collaboration and stakeholder influence skills.
Excellent organizational, time management, and technical writing capabilities.
Values aligned with Eisai’s mission and patient first culture, including integrity, professionalism, quality, and teamwork.
Ability to work a hybrid schedule (a minimum of 3 designated days - T, W, TH - onsite)

Eisai Salary Transparency Language:

The annual base salary range for the Mgr., Product Complaints (Hybrid) is from :$104,900-$137,700

Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan.

Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.

Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.

Certain other benefits may be available for this position, please discuss any questions with your recruiter.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:

Right To Work

E-Verify Participation

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Refine Your Search

eisai jobs

Mgr., Product Complaints (Hybrid)

Associate Director, Government Contracts

QA Specialist (Hybrid)

Manager, Product Training - Oncology

Sr. Manager HRIS - WorkDay

Senior Manager, Data Management

Leader, Field and Sales Training, Alzheimer’s Disease

Director, Translational Science (Neurology)

Manager, Medical Information, Oncology

Administrative Coordinator, Exton Facilities (Onsite)

Associate Director or Director, Medical Science Liaison, Oncology - Central region / Field-based

Associate Director, Translational Science (Neurology)

Global Medical Director, Sleep Disorders - Neurology Global Medical Affairs

Senior Manager, Business Excellence & Asset Management

Director, Organization Development & Learning

Senior Manager, Medical Information, Oncology

Medical Science Liaison (MSL or Sr. MSL), Neurology (Alzheimer's Disease) - Field Based, Central Midwest (KS, NE, IA & MO)

Medical Science Liaison (MSL) / Senior Medical Science Liaison (Sr. MSL), Oncology - Texas; Field-based

Medical Science Liaison, (MSL or Sr. MSL) Neurology (Alzheimer's Disease) - Field Based IL and St. Louis, MO

Associate Director, Discovery IT Portfolio Lead

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