Gilead Sciences Ireland UC Posted November 12, 2026

Sr Manager, Quality Control

Cork, Ireland Full time
Quality Manager
Notify me about similar jobs

Gilead Sciences Ireland UC 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

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfill their aspirations. Join Gilead and help create possible, together.

Job Description

The Sr Manager of QC will report to the Head of QC and will be a key member of the QC leadership team.

QC Operations: Set direction and coordinate QC priorities for the testing and release of raw materials, primary and secondary packaging components, and finished product. Align team delivery with business needs and ensure work is performed in accordance with approved methods, specifications and applicable requirements.

Quality and Compliance: Champion quality and compliance across the team. Establish clear expectations and oversight to ensure laboratory activities and documentation meet cGMP, data integrity, regulatory and applicable pharmacopoeial requirements.

Investigations and CAPA: Lead the team’s response to out-of-specification (OOS) and out-of-trend (OOT) results, deviations, atypical results and laboratory investigations. Provide technical oversight and direction for root-cause analysis, impact assessment and corrective and preventive action (CAPA) support.

Technical Leadership: Provide technical direction and guide sound decision-making in analytical data review, troubleshooting and laboratory problem-solving. Ensure appropriate oversight of analytical methods, instrumentation and controlled laboratory systems.

People Leadership: Lead, coach and develop QC personnel, translating priorities into clear expectations and shared accountability. Build team capability through regular feedback and development support. Empower team members to take ownership and foster open, respectful dialogue and effective collaboration.

Cross-functional Leadership: Represent QC and build alignment with internal and external groups on method transfers, new technologies and equipment. Influence cross-functional decisions by communicating QC priorities and technical information clearly to senior management and external stakeholders, as applicable.

External and Supplier Support: Provide QC leadership in partnerships with external suppliers or quality representatives. Build alignment on the resolution of quality-related issues.

Inspection Readiness: Lead a proactive, inspection-ready laboratory culture with a strong focus on data integrity. Direct the identification of compliance risks, trends and systemic issues through inspection-readiness walkabouts and establish accountability for tracking and addressing appropriate actions.

Continuous Improvement: Champion continuous improvement and operational excellence. Lead the team in identifying and implementing improvements to laboratory processes, efficiency and ways of working while maintaining compliance.

Knowledge:

Excellent communication and strong interpersonal skills are required.

Must be able to participate in highly effective teams.

Must think critically and creatively and be able to work independently, determine appropriate resources for resolution of problems, and have strong organizational and planning skills.

In depth working knowledge of GMPs, pharmacopoeia, and regulatory requirements for testing and validation pertaining to the pharmaceutical industry is required.

Proven leadership ability and problem-solving skills.

In depth knowledge of current industry trends and conventions is required.

Must have excellent analytical and computer skills.

Specific Education & Experience Requirements:

Extensive experience and a BS/MS.

Knowledge and experience in quality control in a highly regulated manufacturing environment is a plus.

Prior people management experience is preferred.

Biopharmaceutical or Pharmaceutical experience is a plus.

Specific Job Responsibilities:

Manages the Quality Control Chemistry laboratory operation, ensuring laboratory processes provide high quality analytical support for manufacturing, maintenance, engineering and validation operations while ensuring compliance of protocols, GMPs, and safety regulations.

Provides broad-based QC Chemistry expertise and counsel to and on behalf of the organization.

Provides leadership, management, and training and career coaching for QC staff.

Responsible for the management, guidance and training of QC Team Leaders, Chemists, Microbiologists and Technicians.

Regularly interacts with senior management or executive levels on matters concerning several functional areas, divisions, and/or customers.

Participates in regulatory audits as required.

Equal Employment Opportunity (EEO)

It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company.  Except if otherwise provided by applicable law, all  employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws).  Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Cork, 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 336 comparable Manager Quality roles across 83 biopharma companies.

336Comparable roles tracked
301Currently active
83Companies hiring similar roles
39Countries represented

Salary context

59 of 336 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 · Advisor, Design Validation & Learning, Biotherapeutics · Lilly $168,000/yr – $268,400/yr
Peer group range $69,550 – $218,200 (median $163,450)

Where these roles are based

Top locations among the 336 comparable roles

United States141
India24
China23
Ireland23
Germany13
United Kingdom11

+ 33 more countries

Seniority mix

336 of 336 peers have a known seniority level

Manager226
Associate67
Associate Director43

Therapeutic area mix

1 of 336 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.

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.

60%
Senior Manager, Global Device Quality
McDermott Laboratories Limited · Northern Cross, Ireland · Manager
Function Therapeutic area Seniority Country
60%
Senior Manager GCP Quality
Regeneron Ireland · Dublin, Ireland · Manager
Function Therapeutic area Seniority Country
60%
Quality Manager (Laboratory)
Abbott · Clonmel, Tipperary, Ireland · Manager
Function Therapeutic area Seniority Country
60%
Manager Quality Assurance
Abbott · Clonmel, Tipperary, 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.