Astellas Pharma Posted November 13, 2026

Quality Assurance Compliance (IE)

IE Type not listed
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Astellas Pharma 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

About Astellas

Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need.  Learn more at Astellas.com .

Are you driven to make a real difference in the lives of patients? 

We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact.

Working Environment and Location

This position is 100% onsite in Tralee, Ireland.

Purpose and Scope

The role is part of the Quality Assurance function within the Astellas Ireland Co. Ltd. Tralee Plant Aseptic Manufacturing Facility.

Responsible for the on-going development, implementation and maintenance of GxP compliance. Responsible for the implementation, execution, and assessment of quality systems, procedures, and records to support compliant GxP operations.

This role will take a lead in supporting the Tralee Plant QMS development and overall maintenance. eQMS metrics development will be a key responsibility area, supporting ICHQ10, Tier 4 and overall QMS Metrics management.

Responsibilities include ensuring adherence to agency regulations (GxP) and guidances, industry best practices, local regulations, and internal policies and procedures.

This position works closely with Validation, Engineering, Manufacturing, Facilities, Document/Data Management, Quality Control (QC) and other GxP supporting functions to ensure compliance.

This is accomplished by direct collaboration and oversight, supporting Validation, Facilities/Engineering, Manufacturing Operations, QC activities and the review/audit of data and reports as specified by Standard Operating Procedures.

This role will support inspection/ audit readiness and coordination of GMP inspection/ audit support activity.

Role and Responsibilities

Quality Management Systems (QMS): Support and maintain the site QMS and eQMS in compliance with GxP requirements, including governance, metrics, risk management, and continuous improvement.

Quality Oversight & Compliance: Review and approve quality records, validation, change controls, and documentation (TrackWise/Vault), ensuring timely investigations and adherence to SOPs and regulatory standards.

Audits & Inspections: Coordinate self-inspections, regulatory, customer, and corporate audits, manage CAPAs, and support inspection readiness, responses, and close-out activities.

Supplier/ Vendor Qualification: Support supplier/ vendor qualification, audits and related eQMS processes.

Quality Programs & Continuous Improvement: Lead initiatives including Product Quality Reviews, Culture of Quality, complaint management, and risk register maintenance to drive operational excellence.

Stakeholder & Regulatory Engagement: Collaborate with cross-functional teams, suppliers, global quality teams, regulatory authorities, and industry groups to ensure effective quality communication and compliance.

Leadership & Team Development: Foster a strong quality culture, influence cross-functional teams, mentor colleagues, and support the development of QA staff and site-wide quality capability.

Essential Qualifications

Science-based degree with relevant experience in a cGMP compliance environment.

Experience within a QA function supporting an aseptic manufacturing plant is essential.

Experience supporting regulatory inspections, customer audits and cross-functional quality systems/ QMS development, management and maintenance is required.

Why Astellas

Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives worldwide.

Real-world patient impact: Contribute to transformative therapies that reach patients around the world, knowing your work makes a difference every day.

Relentless Innovation: Join a company at the forefront of scientific breakthroughs, where you'll have the opportunity to shape the future of healthcare.

A Culture of Growth: Chart your own course within a supportive environment that values your contributions, champions your development, and empowers you to pursue your passions.

Our Organizational Values and Behaviors

Values: Integrity, Innovation and Impact sit at the heart of what we do.

Behaviors: We come together as ‘One Astellas’ , working with courage and a sense of urgency . We are outcome focused and consistently take accountability for our personal contribution.

Our Organisational Values and Behaviours

Integrity

Innovation

Impact

One Astellas

Accountability

Courage

Sense of Urgency

Outcome Focus

Skills and Capabilities

Organizational Focus

Benefits

Careers | Astellas

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help.

#LI-Onsite

#LI-Tralee

#LI-LG1

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
IE
Employment type
Not listed

How this role compares

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

We currently track 1507 comparable Quality roles across 149 biopharma companies.

1507Comparable roles tracked
1371Currently active
149Companies hiring similar roles
53Countries represented

Salary context

263 of 1507 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 $125,500)

Where these roles are based

Top locations among the 1507 comparable roles

United States589
Ireland90
Germany74
China73
France70
India52

+ 47 more countries

Seniority mix

737 of 1507 peers have a known seniority level

Manager227
Senior189
Intern/Fellow/Postdoc99
Associate67
Director46
Associate Director43
Principal34
Senior Director25
Executive/VP7

Therapeutic area mix

3 of 1507 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.

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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.

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.