Find Pharmaceutical quality assurance Jobs in Dublin County Dublin

Senior QA Specialist, Pharmaceutical Development Quality Assurance (Maternity Leave Cover - Remote / Home Based)
Jazz Pharmaceuticals —Dublin, County Dublin
- Bachelor's degree
- Manufacturing
- Communication skills
- Annual leave
QA Manufacturing Analyst
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
Microbiology and Sterility Assurance Lead
Baxter —Dublin, County Dublin
- Management
- Clinic
- Continuous improvement
- Annual leave
2d
GMDP Quality Assurance Manager
WEP Clinical —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Quality Manager / Responsible Person (RP) - Full time
Althera —Dublin, County Dublin
- Full-time
- Doctoral degree
- English
- Bachelor's degree
- Sick pay
Quick apply
4d
Electrical Quality Assurance Inspector (QA)
MSR-FSR —Leixlip, County Kildare
- €60,000–€65,000 a year
- Quality control
- Electrical Engineering
Quick apply
12d
Senior Manager, Quality Assurance - GxP
PTC Therapeutics International Limited —DUBLIN 2, County Dublin
- Full-time
- Microsoft Office
- Bachelor's degree
- Mentoring
Quick apply
2d
QA Team Lead - Shop Floor & Environmental Monitoring (EM)
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- English
- Mentoring
- Manufacturing
Quality Manager
Crown Roofing & Cladding Ltd —Blanchardstown, County Dublin
- Full-time
- Organisational skills
- Construction experience
- Communication skills
- Wellness program
- Employee assistance program
Quick apply
11d
Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based
IQVIA —Dublin, County Dublin
- Doctoral degree
- English
- Research
Release & QP Team Lead
Perrigo —DUBLIN 2, County Dublin
- Writing skills
- Bachelor's degree
- Manufacturing
GMP Team Cleaning Lead (12 Hour Shift)
BidvestNoonan —Dunboyne, County Meath
- 12 hour shift
- English
- Microsoft Office
- Leaving certificate
- Employee discount
Quick apply
Principal, Change Management (Life Sciences) - London or Dublin
Gate One —Dublin, County Dublin
- Hybrid work
- Business development
- Mentoring
- Communication skills
Principal Consultant - Regulatory Affairs
NNIT A/S —Dublin, County Dublin
- Spanish
- Sales
- English
BDS Manufacturing Operations Lead
Alexion Pharmaceuticals,Inc. —Dublin, County Dublin
- Doctoral degree
- Engineering
- Master's degree
Validation Engineer
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Doctoral degree
5d
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Dublin, County Dublin
- Doctoral degree
- Research
- Master's degree
Senior Consultant
NNIT A/S —Dublin, County Dublin
- Spanish
- English
- Master's degree
Associate Director Inspection Management (GCP)
Regeneron —Dublin, County Dublin
- €101,500–€165,200 a year
- Management
- Supervising experience
- Presentation skills
- Annual leave
BDS Operational Resilience & Capacity Lead
Alexion Pharmaceuticals,Inc. —Dublin, County Dublin
- Doctoral degree
- Master's degree
- Bachelor's degree

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Senior QA Specialist, Pharmaceutical Development Quality Assurance (Maternity Leave Cover - Remote / Home Based)

Jazz Pharmaceuticals -
Dublin, County Dublin

Apply Now

Job details

Benefits

Annual leave

Qualifications

Biology
Bachelor's degree
Chemistry
Quality systems
Manufacturing
Communication skills

Full job description

Job Details

Req ID:

R011259

Locations:

Dublin, IE; Belfast, Antrim and Newtownabbey, UK; London, London, City of, UK - [Remote/Home-Based]

Category:

Technical Operations

If you are a current Jazz employee please apply via the Internal Career site.

Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.

Job Description:

This position is part of the PDQA group with the Drug Discovery and Pharmaceutical Development Quality team at Jazz Pharmaceuticals. The position supports the Pharmaceutical Development and Manufacturing Sciences Team (PDMS) in contract manufacturing operations and development of Investigational Medicinal Products (IMPs) and ensures that suitable IMP is provided to the Clinical Trials Supply Management (CTSM) Team for use in clinical trials.

Responsibilities:

The individual is responsible for but not limited to:

Represent PDQA on CMC matrix teams for Jazz development Projects
Monitor the operations at the Contract Manufacturer of IMPs, perform batch review, review product complaints, deviations, change controls and product related investigations (OOS investigations, deviations and CAPAs).
Act as lead auditor in third party vendor audits for IMPs, to include: GMP contract manufacturing, analytical testing and storage facilities when required to ensure compliance with Jazz requirements and country specific regulations.
Managing the product stability programme for IMPs
Develop and write SOPs & controlled documents as required.
Generate and maintain Product Specification Files (PSFs)
Review and approval of product labelling
Build authentic relationships and participate in meetings, as required, with suppliers and contract manufacturers and maintain all product-related, Quality Technical Agreements (QTA’s), QP Agreements and QP Declarations.
Operating supplier management process to include qualification, re-qualification and discontinuation of contractors.
Participate in continuous improvement projects utilising Operational Excellence programs.
Developing and maintaining Quality Systems and ensuring that all operations are fully in compliance with current international standards for cGMP.
Support validation activities.
Supporting CTSM with on time Quality review and approvals to ensure timely supply of clinical material to trial sites.

Other Responsibilities:

Work directly with other key Jazz Pharmaceutical departments to ensure compliance and productive working relationships.
Work closely with other members of Technical Operations organization to ensure delivery of key project objectives and timelines
Contribute to management of the supplier approval program through audit participation and GxP compliance oversight
Assist with troubleshooting quality issues at Partner’s or vendor’s site or associated with technology transfer, when required.
Maintain appropriate Quality Technical Agreements with all GxP vendors
Supporting regulatory submissions

Personal Competencies:

Bachelor's degree in chemistry, biology or a related discipline
Experience working in finished product pharmaceutical/ biologics, including analytical chemistry, quality assurance, quality control, development, and /or manufacturing areas
Experience with third party vendor auditing, complaint handling and change control
Thorough understanding of quality systems and GMP/GDP
Very good oral and written communication skills
Interpersonal skills and professional skills to interact at all levels including senior executives, contractors, and colleagues
Experience working with contract manufacturing
Experience interfacing with regulatory bodies or supporting regulatory submissions

Jazz Pharmaceuticals is an equal opportunity/affirmative action 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 characteristic protected by law.

The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings : https://careers.jazzpharma.com/benefits.html.

Apply Now

Refine Your Search

pharmaceutical quality assurance jobs in dublin county dublin

Senior QA Specialist, Pharmaceutical Development Quality Assurance (Maternity Leave Cover - Remote / Home Based)

QA Manufacturing Analyst

Microbiology and Sterility Assurance Lead

GMDP Quality Assurance Manager

Quality Manager / Responsible Person (RP) - Full time

Electrical Quality Assurance Inspector (QA)

Senior Manager, Quality Assurance - GxP

QA Team Lead - Shop Floor & Environmental Monitoring (EM)

Quality Manager

Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based

Release & QP Team Lead

GMP Team Cleaning Lead (12 Hour Shift)

Principal, Change Management (Life Sciences) - London or Dublin

Principal Consultant - Regulatory Affairs

BDS Manufacturing Operations Lead

Validation Engineer

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Senior Consultant

Associate Director Inspection Management (GCP)

BDS Operational Resilience & Capacity Lead

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