Find Senior associate project Jobs in Cork, C

Sr. Associate Quality Systems Specialist
McKesson —Cork, County Cork
- €40,100–€66,900 a year
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Associate Project Manager
Tetra Tech —Cork, County Cork
- Hybrid work
- Project management
- Contracts
- Leadership
10d
Associate Project Director
Mace —Cork, County Cork
- Full-time
- Hybrid work
- Continuous improvement
- Construction experience
- Leadership
CSA Senior Cost Manager
KPMG —Cork, County Cork
- Weekend availability
- Hybrid work
- Master's degree
- Bachelor's degree
- Mentoring
- Relocation assistance
- Annual leave
Associate Transport Planner
Tetra Tech —Ballincollig, County Cork
- Writing skills
- Master's degree
- Business development
Mask Layout Designer, Staff - Cork, Ireland
Qualcomm —Cork, County Cork
- Computer Science
- Data analysis skills
- Master's degree
- Employee stock purchase plan
14d
Professional Services Engineer - Spanish Speaker
NetApp —Cork, County Cork
- Hybrid work
- Spanish
- Azure
- Doctoral degree
Senior Associate Electrical Engineer
Tetra Tech —Cork, County Cork
- Call to connect
- Project management
- Mentoring
- Manufacturing
Technical Director - Lead MEICA
Tetra Tech —Cork, County Cork
- Engineering
- English
- Mentoring
1d
Quantity Surveyor
AECOM —Cork, County Cork
- Full-time
- Hybrid work
- Master's degree
- Bachelor's degree
- Organisational skills
PWB Designer, Senior - Cork, Ireland
Qualcomm —Cork, County Cork
- Computer Science
- Assembly
- Analysis skills
- Employee stock purchase plan
Professional Services Engineer - German Speaker
NetApp —Cork, County Cork
- Hybrid work
- Azure
- Doctoral degree
- English
Professional Services Engineer - French Speaker
NetApp —Cork, County Cork
- Hybrid work
- Azure
- Doctoral degree
- English
Corporate Counsel
SolarWinds —Cork, County Cork
- Sales
- AI
Quick apply
Associate Director - Mechanical
EDC Engineering Design Consultants LTD. —Cork, County Cork
- Overtime
- Hybrid work
- Master's degree
- Team management
- Leadership
- Annual leave
- Work from home
Quick apply
Associate Director Development Engineering (Civil)
AECOM —Cork, County Cork
- Full-time
- Hybrid work
- Leadership
Associate Engineer - Building Structures
Tetra Tech —Cork, County Cork
- Hybrid work
- Continuous improvement
- Civil Engineering
Associate Electrical Engineer
EDC Engineering Design Consultants LTD. —Cork, County Cork
- Overtime
- Hybrid work
- Engineering
- Microsoft Office
- Master's degree
- Annual leave
- Work from home
Quick apply

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Senior Associate Project Manager
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Sr. Associate Quality Systems Specialist

McKesson -
Cork, County Cork

Apply Now

Job details

€40,100–€66,900 a year

Qualifications

Jira
Microsoft Powerpoint
Microsoft Word
Mandarin
Statistical software
Microsoft Excel
JD Edwards
Engineering
Quality management
Microsoft Office
Minitab
Quality assurance
Bachelor's degree
Sailpoint
Technical writing
Quality systems
AI
Communication skills
ISO 13485

Full job description

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve – we care.

What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you.

About the Role

McKesson Medical-Surgical is seeking a Senior Quality Systems Specialist to support our Quality Management System (QMS) and ensure compliance with medical device regulations and international quality standards. This role is responsible for processing customer complaints, maintaining quality records, supporting audits, administering document control activities, and contributing to continuous improvement initiatives.

The ideal candidate will bring experience in quality assurance within the medical device, pharmaceutical, or regulated healthcare industry and possess a strong understanding of ISO 13485, FDA regulations, CAPA processes, and quality system documentation.

What You'll Do

Quality Systems & Compliance

Maintain and process quality records within the electronic Quality Management System (eQMS), including complaints, CAPAs, deviations, nonconformances, and change controls.
Ensure records are complete, accurate, and properly routed for review and approval.
Support the maintenance and continuous improvement of the Quality Management System (QMS).
Assist in preparing for internal, customer, and regulatory audits.

Customer Complaint Management

Receive, assess, and process product complaints from global customers.
Gather and document relevant information to support complaint investigation activities.
Escalate complaints with potential regulatory impact in accordance with established procedures.
Support timely complaint reporting and documentation compliance.

Document Control & Training

Administer document control activities including issuance, revision, distribution, archival, and obsolescence processes.
Support employee training assignments and training record reconciliation activities.
Monitor and follow up on overdue training requirements.

Investigation & CAPA Support

Compile evidence, timelines, and supporting documentation for investigations.
Contribute to root cause analysis and CAPA activities.
Assist with effectiveness checks and documentation of results.
Support implementation of corrective and preventive actions.

Reporting & Supplier Quality Support

Maintain quality metrics, dashboards, and performance trackers.
Analyze data accuracy and identify discrepancies for correction.
Assist with supplier quality documentation review, SCAR tracking, and audit readiness activities.
Prepare routine reports and quality data summaries for stakeholders.

Basic Requirements

Bachelor's degree in Science, Engineering, Life Sciences, Quality, or a related field or equivalent combination of education and experience.
2+ years of experience in Quality Assurance, Quality Systems, Regulatory Affairs, or a related quality function within a regulated industry.
Experience working in the medical device, pharmaceutical, biotechnology, or healthcare manufacturing industry.
Knowledge of Quality Management Systems (QMS) and electronic quality systems (eQMS).
Experience supporting customer complaints, CAPA, document control, quality records, or audit activities.
Strong written and verbal communication skills.
Proficiency with Microsoft Office applications, including Excel, Word, and PowerPoint.

Preferred Skills & Experience

Experience with ISO 13485:2016 and FDA quality system regulations.
Familiarity with 21 CFR Parts 803, 806, 820, 210, and 211.
Exposure to ISO 14971 and ISO 10993.
Experience with MasterControl, Jira, JDE, OneTrac, SailPoint, Adobe, or similar systems.
Experience supporting supplier quality programs, SCARs, or quality agreements.
Knowledge of cosmetics or dietary supplement regulations.
Experience with AI-enabled productivity tools and statistical software such as Microsoft Copilot, Gemini, or Minitab.
Technical writing experience.
Mandarin language proficiency.
Demonstrated analytical, problem-solving, and project coordination skills.

Travel, Work Environment & Physical Requirements

General office environment.
Candidate must reside in or near Cork, Ireland.
Limited travel may be required.
Flexibility to support U.S.-based business hours when needed.

At McKesson, we care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to supportphysical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse employee population and ensure they are the healthiest versions of themselves.

As part of Total Rewards, we are proud to offer a competitive compensation package at McKesson. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. The pay range shown below is aligned with McKesson's pay philosophy, and pay will always be compliant with any applicable regulations.In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

Our Base Pay Range for this position

€40,100 - €66,900

McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:

McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.

McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.

McKesson job postings are posted on our career site: careers.mckesson.com.

Apply Now

Refine Your Search

senior associate project jobs in cork, c

Sr. Associate Quality Systems Specialist

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