Genzyme Ireland Limited Posted August 24, 2026

Investigation Lead

Waterford, Ireland Full time

Genzyme Ireland Limited 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

Job title: Investigation Lead

Location: Waterford, Ireland

Job type: Onsite, Days

Contract: 23 month Fixed Term Sanofi contract

About the job

Are you passionate about driving a culture of quality, safety, and continuous improvement? Sanofi is seeking an Investigation Lead to join our PFS (Pre-Filled Syringe) Operations team. In this pivotal role, you will act as a role model for our Quality & Safety culture, leading technical and product quality investigations to identify true root causes and implement effective, sustainable corrective actions.

As the responsible person for investigations within your area, you will bring technical expertise, a "right first time" mindset, and a proactive approach to error prevention, all while representing the shift team in engagements with internal and external stakeholders on product quality and safety matters.

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities:

Lead technical and product quality investigations to identify true root causes and implement preventative and corrective actions that ensure zero repeat occurrences

Complete investigations to quality standards within required timeframes, meeting business needs

Facilitate cross-functional investigations on shift using Gemba tools and act as SME for the Investigation System and associated tools

Conduct proactive data collation, trending and analysis to identify process and system improvement opportunities, ensuring adherence to end-to-end lead times

Drive timely closure of deviations, commitments and CAPAs; trend customer complaints to identify effective corrective actions

Act as shift team coach and role model in collaboration with the Compliance Excellence Lead to drive a culture of compliance and continuous improvement

Ensure resolution of and/or appropriate escalation of significant issues; participate in key decision-making in consultation with relevant stakeholders

Provide subject matter expertise and support for systems, technologies and products

Understand shift team supply commitments to ensure on-time completion of investigations

Work closely with shift and process teams to ensure effective, right-first-time document design

Support quality systems operations within assigned area, including conducting and supporting audits (internal, corporate, supplier, customer, regulatory)

Monitor documentation right-first-time performance trends and implement effective CAPAs to prevent reoccurrence

About you

Knowledge of cGMP in a regulated environment

Working knowledge of quality systems in a regulated environment

Sterile manufacturing experience would be very beneficial

System investigation experience

Experience in connection to the remediation process

Excellent accuracy and attention to detail

Excellent interpersonal skills

Problem solving skills

Why choose us?

Make your work count by supporting a company that brings life-changing treatments to millions, and is committed to doing right by patients, communities, and the planet

Advance your career through stretch roles, cross-functional moves, and development opportunities designed to match your ambition

Thrive in inclusive, high-performing teams where every role matters and every voice helps shape what’s next

Pursue Progress . Discover Extraordinary .

Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

#LI-EUR

Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

The salary range for this position is :€31 200,00 - €41 600 Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefit programs.

Job details

Seniority
Not listed
Function
Not listed
Therapeutic area
Not listed
Location
Waterford, Ireland
Employment type
Full time

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