Genzyme Ireland Limited Posted November 3, 2026

Quality Control Support Manager

Waterford, Ireland Full time
Quality Manager
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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: Quality Control Support Manager

Location: Waterford, Ireland

Job Type: 12-Month FTC, Full-Time

Working Arrangements: On-site

About the job

Quality Control (QC) is responsible for sample receipt, testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations. Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation. The Quality Control Operations group supports Laboratory Investigations, Deviation Investigations, CAPA support, Training, and Change Controls. Quality Control Validation Support consists of the Method Validation Group and the Equipment Qualification Group. Quality Control is also responsible for assisting in site wide studies and projects.

Ready to get started?

Join a global network that powers how Sanofi delivers, seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.

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

Overseeing all quality processes and digital solutions related to quality control management in compliance with the Sanofi global processes and quality control tools

Providing QC support for all routine activities

Leading the quality control schedule and capacity planning to support the timely release of products and the adherence of the test’s execution to the committed standard times

Defining and maintaining the maintenance, qualification, and calibration plans to ensure valid status of the lab equipment

Handling sample management flows from sampling to receiving and dispatching to the appropriate labs (including stability and EM sample management per plan)

Managing reference standards and reagents for the labs

Training management of quality control samplers or warehouse/manufacturing samplers when delegated

Ensuring coordination of external/cross site testings, including samples flows and results reports

Owning stability studies managed by the site in compliance with approved protocols: testing executed in a timely manner and stability result trending performed on time, including reports issuance

Providing the appropriate quality control documentation defined in accordance with the Sanofi global processes

Implementing and maintaining QC digital solution (core model and local) (including data management and end-user management)

Managing and training QC support team

Leading initiatives for continuous improvement in QC support processes in coordination with QC Excellence team

Ensuring a quality control process supported by appropriate procedures is implemented in line with global quality and maintained locally in compliance with regulatory requirements

Ensuring the consolidated follow-up and progress tracking of events (e.g., deviation, lab investigations), change control, CAPAs, related to QC, coordinating with respective QC areas and other involved functions, to ensure they are managed and closed as committed

Overseeing the Business Owners for QC processes by having QC representatives of the site in the CoPs led by global, and if requested participating in the CoEs, and ensuring local communication

About you

Bachelor's degree in Electrical Engineering, Mechanical Engineering, Industrial Engineering, or a related discipline.

Significant relevant experience in manufacturing quality, including demonstrated experience in a managerial or leadership role.

Good knowledge of Equipment, systems and quality improvement methodologies.

Strong leadership, analytical, problem-solving, and communication skills.

Six Sigma, or equivalent quality certification is an advantage.

Why choose us?

Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.

Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.

Help deliver 30+ new product launches by 2030, ensuring patients get treatments faster than ever.

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 :€73 200,00 - €97 600 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
Manager
Function
Quality
Therapeutic area
Not listed
Location
Waterford, Ireland
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 332 comparable Manager Quality roles across 83 biopharma companies.

332Comparable roles tracked
292Currently active
83Companies hiring similar roles
40Countries represented

Salary context

56 of 332 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate I, Quality Control, Raw Materials · ModernaTX, Inc. $53,500/yr – $85,600/yr
Highest disclosed · Assoc Director, Quality Assurance · Gilead Sciences, Inc. $182,070/yr – $235,620/yr
Peer group range $69,550 – $208,845 (median $166,200)

Where these roles are based

Top locations among the 332 comparable roles

United States135
India28
China23
Ireland23
Germany13
Japan11

+ 34 more countries

Seniority mix

332 of 332 peers have a known seniority level

Manager222
Associate65
Associate Director45

Therapeutic area mix

1 of 332 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
McDermott Laboratories Limited Northern Cross, Ireland Manager
Same function Same seniority Same country
60%similar
Mylan Teoranta Inverin, Ireland Manager
Same function Same seniority Same country
60%similar
AbbVie Sligo, SO Manager
Same function Same seniority Same country
60%similar
Regeneron Ireland Dublin, Ireland Manager
Same function Same seniority Same country
60%similar
Regeneron Ireland Remote, Ireland Manager
Same function Same seniority Same country
60%similar
AbbVie Dublin, County Dublin Manager
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Senior Manager, Global Device Quality
McDermott Laboratories Limited · Northern Cross, Ireland · Manager
Function Therapeutic area Seniority Country
60%
QA Operations Manager
AbbVie · Sligo, SO · Manager
Function Therapeutic area Seniority Country
60%
Quality Assurance Compliance Manager
AbbVie · Dublin, County Dublin · Manager
Function Therapeutic area Seniority Country
60%
TPM Quality Manager
Abbott · Ireland · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.