Find Pharmaceutical learning development Jobs in Dublin County Dublin

QA Manager & Qualified Person (QP)
RxSource —Dublin, County Dublin
- Engineering
- Bachelor's degree
- No degree
Tech Transfer Lead, Drug Substance
PSC Biotech —Dublin, County Dublin
- Full-time
- Doctoral degree
- Master's degree
- Project management
5d
Manager GD Training Systems
Regeneron —Dublin, County Dublin
- €74,000–€120,700 a year
- Bachelor's degree
- Annual leave
Senior Specialist MS&T
PSC Biotech —Dublin, County Dublin
- Data analysis skills
- Master's degree
- Bachelor's degree
4d
Senior Critical Environment Technician - Day Shift
Microsoft —Dublin, County Dublin
- €24.71–€35.43 an hour
- Weekend availability
- Azure
- Assembly
- No degree
Specialist Medical Scientist, Chemistry / Electrophoresis
ICON Plc —Dublin, County Dublin
- Overtime
- Master's degree
- Bachelor's degree
- No degree
1d
Programme Director MSc in Procurement and Supply Chain Management
Griffith College —DUBLIN 8, County Dublin
- Full-time
- Management
- Doctoral degree
- Master's degree
- Free parking
- Work from home
Quick apply
11d
UKI Business Consulting - Life Sciences, SC/AM
EY —DUBLIN 2, County Dublin
- Full-time
- Hybrid work
- Master's degree
- Business
- Gym membership
- Referral programme
Support Pharmacist
Boots —Dublin, County Dublin
- Full-time
- Employee discount
NeoDyne Engineering Graduate Programme Dublin 2026
NeoDyne —Dublin, County Dublin
- Overtime
- AutoCAD
- Customer service
- Engineering
Quick apply
Sales Specialist
IQVIA —Dublin, County Dublin
- Full-time
- Business
- Communication skills
- Annual leave
12d
Project Management Officer - Lead
Eurofins —Dublin, County Dublin
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Quick apply
Contracts Manager - Ireland/European/UK Projects
Crown Global —Dublin, County Dublin
- Full-time
- Microsoft Office
- Bachelor's degree
- Organisational skills
- Annual leave
Quick apply
UKI Business Consulting - Life Sciences, Commercial Strategy, Market Access, R&D Medical, SM
EY —DUBLIN 2, County Dublin
- Full-time
- Hybrid work
- English
- Master's degree
- No degree
- Gym membership
- Referral programme
Lead Tech, Operations
MSD —Dunboyne, County Meath
- Full-time
- Hybrid work
- Bachelor's degree
- Manufacturing
- Leadership
2h
Electrical Apprentice
Amgen —Dún Laoghaire, County Dublin
- Maintenance
- English
- Leaving certificate
14d
Director Regulatory Compliance (Process Excellence)
Viatris —Northern Cross, County Dublin
- Full-time
Project Engineer
Embecta —Dún Laoghaire, County Dublin
- Full-time
- Engineering
- Bachelor's degree
- Communication skills
4h
Key Account Manager
IQVIA —Dublin, County Dublin
- Full-time
- Analysis skills
Validation Engineer
CAI —Dublin, County Dublin
- Full-time
- Engineering
- Bachelor's degree
- Communication skills
Quick apply

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QA Manager & Qualified Person (QP)

RxSource
Dublin, County Dublin

Apply Now

Job details

Qualifications

Engineering
Bachelor's degree
Packaging
Quality systems
Manufacturing

Full job description

At RxSource, our culture of appreciation and hard work fuels our success in improving patient's lives.
Join us and be recognized for your contributions to our purpose-driven movement.

Why Work for RxSource?

Our Culture

We have a supportive and welcoming culture that believes in giving back. We offer a paid days leave for volunteering to improve the lives of patients.

Fun-Filled Workplace

With team-building events and your birthday day off, we aim to provide a dynamic and enjoyable work experience for all employees. Join us and discover a fresh perspective on work.

Own-it

With our "Own It" mentality, we encourage responsibility, continuous learning, and growth. And to help you on your journey, we offer reimbursement for courses and training for professional development.

QA Manager & Qualified Person (QP)
Dublin, Ireland

Description

Position Summary:

The QA Manager & Qualified Person (QP) is the senior Quality representative at the Dubin, Ireland facility and is responsible for the effective implementation, maintenance, and continuous improvement of the site Pharmaceutical Quality System (PQS) locally. This role provides quality oversight of GMP/GDP operations supporting packaging, labeling, QP certification, and distribution of investigational medicinal products (IMPs) in support of clinical trials.

In addition, this role performs Qualified Person (QP) duties in accordance with EU GMP, Annex 13, Annex 16, the Manufacturing/Importation Authorization (MIA), and applicable EU and national legislation, certifying IMP batches for release for clinical trial use.

The role serves as the primary site Quality lead, supporting inspections, audits, supplier qualification, quality events management, and training, while partnering cross?functionally to embed a strong culture of quality and compliance. On?site Quality personnel will report to the QA Manager & Qualified Person (QP).

Responsibilities:

QA Manager Responsibilities:

Ensure ongoing compliance with EU GMP, GDP, HPRA expectations, and internal SOPs.
Maintain and continuously improve the site Pharmaceutical Quality System (PQS).
Act as Quality lead for the Dubin facility, providing daily QA oversight of operations.
Review and approve controlled documents such as SOPs and work instructions.
Provide QA oversight for clinical trial related services, including receipt, storage, label printing, secondary packaging and labeling, and distribution of products used in clinical trials.
Review and approve clinical packaging and labeling batch documentation.
Provide QA oversight of activities such as temperature monitoring, sanitation, environmental controls, calibration, and preventive maintenance.
Ensure GMP/GDP facilities, systems, and equipment maintain a qualified/validated state.
Review, approve, and manage deviations, CAPAs, change controls, risk assessments, complaints, and investigations within the EQMS ensuring data integrity and timely closure.
Lead or support root cause investigations and ensure timely, effective corrective and preventive actions.
Support and execute product recalls in accordance with SOPs and legal/regulatory guidance when required.
Host and support customer audits, regulatory inspections, and internal self?inspections.
Ensure inspection readiness and timely, compliant responses to audit observations.
Serve as a Quality point of contact for customers and regulatory authorities as needed.
Qualify, assess, and monitor suppliers and service providers using a risk-based approach.
Review and maintain Quality Agreements / Technical Agreements with suppliers and customers.
Develop, deliver, and oversee GMP/GDP and SOP training programs and assess training effectiveness.
Assess training effectiveness and identify ongoing training needs.
Assist in recruiting, onboarding, coaching, and mentoring Quality team members.
Promote a proactive quality culture across all functions and levels.
Drive continuous improvement initiatives to enhance compliance, efficiency, and quality performance.
Track, trend, and report quality metrics to senior management and support management review activities.
Stay current with changes in US and global pharmaceutical regulations, guidance, and industry best practices.

Qualified Person Responsibilities:

Act as a named Qualified Person on the site MIA and perform QP duties as defined in site SOPs and Quality Agreements.
Certify and release IMP batches in accordance with EU GMP, Annex 13, Annex 16, CTA/IMPD requirements, and national legislation.
Ensure that all manufacturing, testing, packaging, and supply chain activities comply with EU GMP and the approved clinical trial authorization.
Verify that manufacturing and testing sites are appropriately authorized and GMP compliant.
Confirm completeness and compliance of batch documentation, investigations, validations, and QC data prior to certification.
Ensure appropriate qualification of starting materials, packaging materials, and suppliers.
Maintain appropriate oversight of any delegated QP?related activities, retaining full accountability for certification decisions.
Maintain up?to?date QP training and ensure ongoing regulatory and product knowledge.

Qualifications:

Required:
Bachelor’s degree in Pharmacy, Life Sciences Engineering, or a related discipline.
Educational qualifications meeting EU QP eligibility requirements as defined in Directives 2001/83/EC and applicable national legislation.
5+ years of Quality experience in pharmaceutical manufacturing, clinical trial packaging and labeling, pharmaceutical distribution within a GxP environment.
Strong working knowledge of EU GMP, Annex 13, Annex 16, GDP, and HPRA expectations.
Experience managing quality systems, audits, deviations, CAPAs, and change control.
Proven ability to work cross?functionally and manage multiple priorities.

Preferred:

Prior experience in a clinical trial supply services organization.
Experience serving as a named QP on an MIA IMP.
Experience leading or developing other Quality professionals.

Apply Now

Refine Your Search

pharmaceutical learning development jobs in dublin county dublin

QA Manager & Qualified Person (QP)

Tech Transfer Lead, Drug Substance

Manager GD Training Systems

Senior Specialist MS&T

Senior Critical Environment Technician - Day Shift

Specialist Medical Scientist, Chemistry / Electrophoresis

Programme Director MSc in Procurement and Supply Chain Management

UKI Business Consulting - Life Sciences, SC/AM

Support Pharmacist

NeoDyne Engineering Graduate Programme Dublin 2026

Sales Specialist

Project Management Officer - Lead

Contracts Manager - Ireland/European/UK Projects

UKI Business Consulting - Life Sciences, Commercial Strategy, Market Access, R&D Medical, SM

Lead Tech, Operations

Electrical Apprentice

Director Regulatory Compliance (Process Excellence)

Project Engineer

Key Account Manager

Validation Engineer

I want to receive the latest job alerts for pharmaceutical learning development in dublin county dublin

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Explore jobs in more locations

At RxSource, our culture of appreciation and hard work fuels our success in improving patient's lives.
Join us and be recognized for your contributions to our purpose-driven movement.

Why Work for RxSource?

Our Culture

Fun-Filled Workplace

Own-it

QA Manager & Qualified Person (QP)
Dublin, Ireland

QA Manager & Qualified Person (QP)

Description

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pharmaceutical learning development jobs in dublin county dublin

I want to receive the latest job alerts for pharmaceutical learning development in dublin county dublin

Related Searches

Explore jobs in more locations

At RxSource, our culture of appreciation and hard work fuels our success in improving patient's lives. Join us and be recognized for your contributions to our purpose-driven movement.

Why Work for RxSource?

Our Culture

Fun-Filled Workplace

Own-it

QA Manager & Qualified Person (QP)

Description

At RxSource, our culture of appreciation and hard work fuels our success in improving patient's lives.
Join us and be recognized for your contributions to our purpose-driven movement.