Find pharmaceutical quality control Jobs in dublin, d

QA Manager & Qualified Person (QP)
RxSource —Dublin, County Dublin
- Engineering
- Bachelor's degree
- No degree
Turnover Manager
Fohntech Group —DUBLIN 15, County Dublin
- Full-time
- No degree
- Construction
6d
Quality Engineering Manager
Embecta —Dún Laoghaire, County Dublin
- Full-time
- Engineering
- Communication skills
Quality Manager, Global Distribution Quality
Amgen —Dublin, County Dublin
- Doctoral degree
- Master's degree
- Bachelor's degree
Project Scheduler - CMC
Sia —Dublin, County Dublin
- Full-time
- Hybrid work
- Engineering
- Project management
- Bachelor's degree
Quick apply
Operations Technician
Charles River Laboratories —Dublin, County Dublin
- Full-time
- Sales
- Microsoft Office
- No degree
- Annual leave
8d
GMDP Quality Assurance Manager
WEP Clinical —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Director Regulatory Affairs Global CMC
Viatris —Northern Cross, County Dublin
- Full-time
- Project management
- Mentoring
- Manufacturing
Microbiologist - 12 Month FTC
Embecta —Dún Laoghaire, County Dublin
- Full-time
- Microsoft Office
- Analysis skills
- Manufacturing
Test Pack Manager
Fohntech Group —DUBLIN 15, County Dublin
- Full-time
- Bachelor's degree
Process Engineer ( 12 Months Agency Contract )
Viatris —Damastown, County Dublin
- Full-time
- Engineering
- Bachelor's degree
- Manufacturing
Geo-Environmental Consultant
AECOM —Dublin, County Dublin
- Full-time
- Hybrid work
- Engineering
- Bachelor's degree
- Communication skills
Senior Project Engineer (QC Lab Equipment) / West Dublin / Biopharma
PM Group —Dublin, County Dublin
- Engineering
- Project management
- Quality control
Sr. Manager, Medical Writing
Alfasigma Group —Dublin, County Dublin
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
14d
Basic Grade Pharmacist
Beaumont Hospital —Dublin, County Dublin
- €49,985–€78,433 a year
- Weekend availability
5d
Business Development and Pre-sales SME
Tata Consultancy Services —Dublin, County Dublin
- Call to connect
- Sales
- Business development
- Manufacturing
Territory Manager in Training -Life Science
Ecolab Inc. —Dublin, County Dublin
- Full-time
- Customer service
- English
- Microsoft Office
- Life insurance
8d
Warehouse Operator
Charles River Laboratories —Dublin, County Dublin
- Full-time
- Leaving certificate
- No degree
- Organisational skills
- Annual leave
- Employee discount
Global Lead Auditor
Uniphar PLC —DUBLIN 24, County Dublin
- Full-time
- Leadership
- Communication skills
Quick apply
CQV Engineer
IPS-Integrated Project Services —DUBLIN 12, County Dublin
- Full-time
- Engineering
- Bachelor's degree
4d

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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 quality control jobs in dublin, d

QA Manager & Qualified Person (QP)

Turnover Manager

Quality Engineering Manager

Quality Manager, Global Distribution Quality

Project Scheduler - CMC

Operations Technician

GMDP Quality Assurance Manager

Director Regulatory Affairs Global CMC

Microbiologist - 12 Month FTC

Test Pack Manager

Process Engineer ( 12 Months Agency Contract )

Geo-Environmental Consultant

Senior Project Engineer (QC Lab Equipment) / West Dublin / Biopharma

Sr. Manager, Medical Writing

Basic Grade Pharmacist

Business Development and Pre-sales SME

Territory Manager in Training -Life Science

Warehouse Operator

Global Lead Auditor

CQV Engineer

I want to receive the latest job alerts for pharmaceutical quality control in dublin, d

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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 quality control jobs in dublin, d

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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)

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.