Genzyme Ireland Limited Posted November 6, 2026

Quality Graduate

Waterford, Ireland Full time
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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

Location: Waterford, Ireland

Start Date: 1 September 2027

Duration: 23 months | Two 8-month rotations, and 7-month

Working Model: on-site

Working Hours: Full-time

Salary:  €41,600 gross per annum

Assessment Centre: January 2027 | In person, Waterford

Your opportunity at Sanofi

Ready to turn your academic knowledge into real-world experience?

Join Sanofi, a global biopharmaceutical company, through our 23-month Graduate Programme in Waterford. Explore three different functions, gain hands-on industry experience and develop the skills to shape your future career.

Quality Systems & Compliance is at the heart of delivering safe, effective, and compliant healthcare products to patients worldwide. This programme offers graduates the chance to build expertise in quality management, problem-solving, and regulatory excellence while making a tangible impact on product quality and operational performance.

One programme. Three rotations. A world of experience.

Why explore just one area when you could experience three?

Our structured Graduate Programme takes you through two 8-month rotations, and 7-month , providing exposure to different functions, meaningful projects and opportunities to learn from experienced professionals.

Your rotation journey

Rotation 1: Quality Systems & Data Integrity | Months 1–8

Start your journey in Quality Systems, where you'll gain an understanding of GMP compliance, data integrity principles, and quality documentation processes that help ensure the safe and reliable manufacture of healthcare products.

Support the Data Integrity Quality Improvement Programme (QIP) through quality systems, documentation, and compliance activities.

Conduct routine GMP and data integrity checks, helping to identify and address quality issues while ensuring proper documentation practices are followed.

Assist with technical writing, document management, CAPA follow-up activities, and initiatives that strengthen inspection readiness and continuous improvement across the site.

Rotation 2: Compliance | Months 9–16

Build your expertise in Compliance, working closely with teams responsible for maintaining inspection readiness and ensuring adherence to GMP and regulatory requirements.

Participate in internal audits and compliance assessments, helping identify opportunities for process improvements.

Support inspection readiness activities by reviewing documentation, tracking actions, and coordinating with operational teams.

Monitor SOP compliance and contribute to initiatives that strengthen quality culture and regulatory adherence across the site.

Rotation 3: Advanced QMS & Compliance Projects | Months 17–23

In your final rotation, you'll take on more ownership through strategic quality and compliance projects, applying the knowledge and skills developed throughout the programme.

Lead or support complex CAPA investigations, identifying root causes and implementing sustainable corrective actions.

Coordinate audit activities, working with stakeholders to prepare documentation, track commitments, and support successful outcomes.

Contribute to cross-site quality initiatives, such as QMS harmonization projects, process improvements, or compliance enhancement programmes with regional or global impact.

Your development focus

Throughout the programme, you'll develop knowledge and practical skills to support your future career in Quality Systems and Compliance, building the expertise required to ensure products, processes, and quality systems meet the highest regulatory and operational standards.

Develop a strong understanding of quality management principles, regulatory requirements, GMP compliance, and Quality Management Systems (QMS) within a highly regulated industry.

Strengthen cross-functional collaboration, communication, project management, and stakeholder engagement skills through exposure to diverse teams and business processes.

Build expertise in risk assessment, problem-solving, root cause analysis, CAPA management, auditing, and continuous improvement methodologies to support effective decision-making and operational excellence.

Your growth, our commitment

Your development is at the heart of our programme. Here's what you can look forward to:

Three diverse rotations: Explore different functions and build a broader understanding of the business.

Dedicated cross-functional mentor: Receive guidance from an assigned mentor, with monthly check-ins throughout the programme.

A buddy in every rotation: Get practical, day-to-day support as you settle into each new team.

Hands-on training: Learn directly from experienced colleagues and develop skills through practical experience and training opportunities.

Who we're looking for

We're looking for curious, motivated graduates who are eager to learn, collaborate and explore new opportunities.

To be eligible, you'll need to:

Have graduated within the past two years or be due to graduate before 1 September 2027.

Hold a minimum 2.1 primary degree or a Master's degree in a relevant discipline such as Quality Assurance, Pharmaceutical Sciences, Biological Sciences, Chemistry, Biotechnology, Microbiology, Engineering, or a related Life Sciences field.

Have full, unrestricted right to work in Ireland.

Essential skills:

Strong analytical and problem-solving skills with the ability to assess risks and identify effective solutions.

Excellent communication and collaboration skills, with the confidence to work across diverse teams and stakeholders.

Strong organisational and project management skills, with the ability to manage multiple priorities in a fast-paced environment.

High attention to detail and a commitment to quality, compliance, and continuous improvement.

Desirable qualifications:

Previous internship, placement, research, or work experience within a regulated industry such as pharmaceuticals, biotechnology, medical devices, or healthcare.

Knowledge of Quality Management Systems (QMS), GMP requirements, or regulatory compliance principles.

Experience participating in quality improvement, auditing, process improvement, or compliance-related projects.

Demonstrated leadership experience through academic, extracurricular, or professional activities.

Previous experience through internships, placements or relevant work is an advantage, but not essential.

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.

What we offer

Alongside structured professional development, you'll receive:

Annual salary: €41,600 gross per annum

Bonus: Performance related bonus 8% (STI)

Benefits: Access to an attractive benefits package.

Your recruitment journey

We want you to know what to expect at every step:

Apply & complete a short survey: After applying, you'll receive a mandatory screening survey.

On-demand video interview: Selected candidates can record their responses at a convenient time within the given deadline.

Short connect call: An informal conversation with our recruitment team to discuss your application and confirm a few details.

In-person assessment centre: Final assessments are planned for January 2027 at our Waterford site.

Candidates will be assessed at each stage, with progression to the next step depending on the outcome. Further details will be shared with those progressing.

Ready to start your journey?

You don't need to have your whole career figured out. If you're curious, eager to learn and excited to explore what the pharmaceutical industry has to offer, we'd love to hear from you.

Three rotations. Two years. Your future starts here.

Apply now and start your journey with Sanofi!

#LI-EUR

#LI-Onsite

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 !

Job details

Seniority
Not listed
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 1502 comparable Quality roles across 147 biopharma companies.

1502Comparable roles tracked
1357Currently active
147Companies hiring similar roles
54Countries represented

Salary context

261 of 1502 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · QC Lab Technician (Lilly Contractor - Fixed Term) · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $43,753 – $350,000 (median $123,250)

Where these roles are based

Top locations among the 1502 comparable roles

United States589
Ireland87
Germany72
China72
France67
India57

+ 48 more countries

Seniority mix

731 of 1502 peers have a known seniority level

Manager223
Senior189
Intern/Fellow/Postdoc98
Associate65
Director46
Associate Director45
Principal33
Senior Director25
Executive/VP7

Therapeutic area mix

3 of 1502 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease2
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.

40%similar
McDermott Laboratories Limited Northern Cross, Ireland Manager
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Manager
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Senior
Same function Same country
40%similar
Regeneron Ireland Limerick, Ireland Senior
Same function Same country
40%similar
Regeneron Ireland Limerick, Ireland
Same function 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.

Or follow a whole field: get every new Quality job in Ireland, and choose locations and companies.

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.

40%
Senior Manager, Global Device Quality
McDermott Laboratories Limited · Northern Cross, Ireland · Manager
Function Therapeutic area Seniority Country
40%
Senior Microbiology Team Lead
Mylan Teoranta · Inverin, Ireland · Senior
Function Therapeutic area Seniority Country
40%
Senior QA Validation Specialist
Regeneron Ireland · Limerick, Ireland · Senior
Function Therapeutic area Seniority Country
40%
Supervisor Quality Control (Microbiology)
Regeneron Ireland · Limerick, Ireland · Seniority not listed
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.