Find Process science shift team lead Jobs in Ireland

Quality Assurance Associate Specialist
MSD —Carlow, County Carlow
- Full-time
- Hybrid work
- Engineering
- Quality control
- Manufacturing
4d
Quality Supervisor
C&D Foods & Affiliates —Edgeworthstown, County Longford
- Full-time
- Oracle
- ERP systems
- Supervising experience
Quick apply
4d
Associate Director, Commercial Launch & Project Management
Regeneron —Dublin, County Dublin
- €101,500–€165,200 a year
- Microsoft Office
- Master's degree
- Project management
- Annual leave
Quality Assurance Technician
Kepak Group —Cavan, County Cavan
- Full-time
- English
- Microsoft Office
- No degree
- Employee discount
- Referral programme
Quick apply
Shift Manager
Kinisla —Charleville, County Cork
- 12 hour shift
- Microsoft Office
- IT
- Communication skills
- Annual leave
Quick apply
Senior Manager Logistics Process Integration
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- Master's degree
- Analysis skills
- Annual leave
- Work from home
Operations Leader (OSD Manufacturing)
AbbVie —Sligo, County Sligo
- Overtime
- Engineering
- Supervising experience
- No degree
Team Leader
Jabil Circuit —Bray, County Wicklow
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
2h
Operations Quality Shift Lead
Abbott Laboratories —Kilkenny, County Kilkenny
- Full-time
- Engineering
- No degree
- Manufacturing
5d
Major Incident Manager ,Assistant Vice President
State Street —Kilkenny, County Kilkenny
- Weekend availability
- Computer Science
- Windows
- Master's degree
QC In Process People Team Leader
GE HEALTHCARE —Cork, County Cork
- No degree
- Leadership
- Communication skills
- Annual leave
Operations Manager
Catalyx —Cork, County Cork
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
Quick apply
Head of Phenomics
Novartis —Dublin, County Dublin
- €102,200–€189,800 a year
- Full-time
- Hybrid work
- Doctoral degree
- Computer Science
- Master's degree
Senior Engineer, Integration & Control
West Pharmaceutical Services —Waterford, County Waterford
- €65,900–€83,800 a year
- Day shift
- AutoCAD
- Computer Science
- CAD
Field Excellence Manager
Novartis —Dublin, County Dublin
- €60,830–€112,970 a year
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
EHS Manager
BD —Limerick, County Limerick
- €75,900–€115,725 a year
- Continuous improvement
- Leadership
- Communication skills
Senior Expert Data Science, Scientific Innovation
Novartis —Dublin, County Dublin
- €63,490–€117,910 a year
- Full-time
- Hybrid work
- Research
- No degree
- AI
Senior Expert Data Science, AI Methods
Novartis —Dublin, County Dublin
- €63,490–€117,910 a year
- Full-time
- Hybrid work
- Computer Science
- Master's degree
- Bachelor's degree
Manager, Digital Optimization - Campaign Tagging Lead
Novartis —Dublin, County Dublin
- €57,120–€106,080 a year
- Full-time
- Team management
- Leadership
- Communication skills
Clinical Document Management Learning Manager
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- Research
- Bachelor's degree
- No degree
13d

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Quality Assurance Associate Specialist

MSD -
Carlow, County Carlow

Apply Now

Job details

Full-time
4 days ago

Qualifications

Engineering
Quality assurance
Quality control
Technical writing
Manufacturing
Leadership

Full job description

Job Description

Our facility in Carlow site broke ground in 2008 and is a filling site for the launch and commercial supply of vaccines, biologics and small molecule drug product. Since its initial launch, the site has attracted significant internal investment and is now home to several state-of-the-art production facilities, laboratories and temperature-controlled warehousing units. The Carlow site is a significant employer in the Southeast region and attracts high performing talent through close collaborations with universities and colleges in the region.
Our Carlow site has another great opportunity for a Quality Assurance Associate Specialist within IPT. Reporting to the Quality Manager, you will provide essential QA oversight and support across the site.

What you will do:
Bring energy, knowledge, innovation, and leadership to carry out the following:

Review and approval of all manufacturing batch documentation including electronic batch records, real time reports, master data using the site systems.
Review and approval of SOPs, cleaning verification/validation data and other documents as necessary for the IPT department.
Drive effective writing/revising/ rolling out of accurate operational procedures, training materials and maintenance procedures for various Quality related systems; ensure all work is subsequently carried out in line with same.
Support the development and implementation of improved quality reporting measures.
Liaise with the Quality Specialists/QP/QA Lead to resolve queries relating to batch manufacturing process.
Actively participate in Plant/Quality committees and works with other site functional

groups, such as the Microbiology Laboratory, Production, Utilities, Site Services, and
Maintenance to help set direction for plant wide GMP initiatives.

Provide effective real time on the floor support for day-to-day manufacturing operations for example area clearances, batch record reviews, aseptic operations.
Provide quality support across the site, including training and guidance on company guidelines, policies, and regulatory interpretation.
Partner with colleagues cross functionally to provide support and advice on day-to-day basis and on a project, basis including communications, training, project work,

audit/inspection duties, investigations, batch work, customer queries etc.; thereby ensuring IPT is audit/inspection ready.

Initiate and maintain quality related metrics, ensuring effective communication and

follow up of same, including Monitoring of quality systems, the self-inspection program, verification of the effective implementation of key GMP programs, effectiveness of Preventative Actions.

Leadership activities including selection, development, coaching, and day to day management. Ensure that the team receives appropriate resources and programs to develop technical and other skills, to complete their jobs whilst stimulating personal growth and development in line with role. Develop and maintain training programs.
Work collaboratively to drive a safe and compliant culture in Carlow.
Work shift patterns in line with manufacturing operations to ensure Quality oversight as required.
The above list of duties is not an exhaustive list

In order to excel in this role, you will more than likely have:

Degree in Science, Engineering or in a relevant disciplineORequivalent experience with operational excellence in GMP environment
A minimum of 3 years’ experience in Quality Control, Quality Assurance or Pharmaceutical or manufacturing
Working knowledge of regulatory and code requirements pertaining to Irish, European, and International Codes, Standards, and Practices.
Knowledge of cGMP and GDP is essential.
Proficiency in report writing, standards development, and policy writing.

Please dont hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.
Please feel free to speak to us about what flexibility means to you during your application.

So, if you are ready to:
Invent solutions to meet unmet healthcare needs,please apply today.

Required Skills:
Analytical Problem Solving, Aseptic Filling, cGMP Compliance, Complaint Management, Compliance Programs, Continuous Process Improvement, Decision Making, Deviation Management, Documentation Review, GMP Compliance, Good Manufacturing Practices (GMP), Operational Efficiency, Production Operations, Quality Auditing, Quality Management, Quality Management Standards, Quality Management System Auditing, Quality Management System Improvement, Quality Management Systems (QMS), Quality Standards, Quality Support, Regulatory Requirements, Root Cause Analysis (RCA), Technical Writing, Training and Development

Preferred Skills:
Current Employees applyHERE

Current Contingent Workers applyHERE

Search Firm Representatives Please Read Carefully
Merck Co., Inc., Rahway, NJ, USA, also known as Merck Sharp Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:
Regular

Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not Applicable

Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
07/20/2026*A job posting is effective until 11:59:59PM on the dayBEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFORE the job posting end date.
Requisition ID: R398536

Apply Now

Refine Your Search

process science shift team lead jobs in ireland

Quality Assurance Associate Specialist

Quality Supervisor

Associate Director, Commercial Launch & Project Management

Quality Assurance Technician

Shift Manager

Senior Manager Logistics Process Integration

Operations Leader (OSD Manufacturing)

Team Leader

Operations Quality Shift Lead

Major Incident Manager ,Assistant Vice President

QC In Process People Team Leader

Operations Manager

Head of Phenomics

Senior Engineer, Integration & Control

Field Excellence Manager

EHS Manager

Senior Expert Data Science, Scientific Innovation

Senior Expert Data Science, AI Methods

Manager, Digital Optimization - Campaign Tagging Lead

Clinical Document Management Learning Manager

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