Find Science shift team Jobs in Dublin, D

Sr Biopharmaceutical Rep-Repatha-Nanning
Amgen —Dún Laoghaire, County Dublin
- €69,614.15–€94,183.85 a year
- Analysis skills
- Supervising experience
- Project management
14d
Manufacturing Technologist
Ipsen Manufacturing Ireland Ltd —Dublin, County Dublin
- Full-time
- Bachelor's degree
3d
Senior Manager, Operations Supply Planner
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- ERP systems
- Analysis skills
Senior Expert (Rapid Prototyping)
Novartis —Dublin, County Dublin
- €63,490–€117,910 a year
- Full-time
- Hybrid work
- AI
- Python
Social Care Leader
Ann's Childrens Care —Dublin, County Dublin
- Up to €45,000 a year
- Full-time
- Childcare
- Experience working with children
- No degree
Quick apply
2d
Senior Principal Developer
Novartis —Dublin, County Dublin
- €63,490–€117,910 a year
- Full-time
- Hybrid work
- English
- Master's degree
- Software development
Manager, Engineering (Backend Development)
Sonatus —Dublin, County Dublin
- Computer Science
- Engineering
- Java
- Annual leave
- Life insurance
Quick apply
Systems Architect – Connected Medical Devices (Interface Architect)
ResMed —Dublin, County Dublin
- Full-time
- Engineering
- Software development
- Agile
- Referral programme
Manager, Digital Optimization - Campaign Tagging Lead
Novartis —Dublin, County Dublin
- €57,120–€106,080 a year
- Full-time
- Team management
- Leadership
- Communication skills
PM2 Manufacturing Manager (Days)
Amgen —Dún Laoghaire, County Dublin
- €78,613.10–€106,358.90 a year
- Engineering
- English
- Bachelor's degree
3d
Defect equipment Systems Engineer
Intel —Leixlip, County Kildare
- €59,200–€111,300 a year
- Full-time
- Software troubleshooting
- Engineering
- Data analysis skills
7d
Clinical Development Medical Director - Neuromuscular
Novartis —Dublin, County Dublin
- €90,300–€167,700 a year
- Full-time
- Hybrid work
- Research
- Leadership
- Communication skills
Senior Project Manager, GSC Business Performance & Transformation
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- Master's degree
- Project management
- Annual leave
6d
Global Head of Talent Acquisition
Mercury Engineering —Dublin, County Dublin
- Master's degree
- Bachelor's degree
- Business
TFSM IR EHS Safety and Industrial Hygiene Engineer
Intel —Leixlip, County Kildare
- €59,200–€111,300 a year
- Full-time
- Microsoft Excel
- Engineering
- Analysis skills
Director, Software Engineering
Mastercard —Dublin, County Dublin
- Full-time
- Computer Science
- Bachelor's degree
- No degree
Global Labelling Director, Content
Novartis —Dublin, County Dublin
- €90,300–€167,700 a year
- Full-time
- Hybrid work
- Leadership
Senior Manager, Supplier Compliance & Third Party Risk Management (TPRM) – Global Procurement
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- Master's degree
- Analysis skills
- Annual leave
Senior Manager, Serialization Data Operations
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- ERP systems
- Bachelor's degree
10d
Sr. Director & Head of Architecture
G-P —Dublin, County Dublin
- €160,800–€201,000 a year
- Full-time
- Remote
- Computer Science
- Master's degree
- AWS
Quick apply

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Sr Biopharmaceutical Rep-Repatha-Nanning

Amgen -
Dún Laoghaire, County Dublin

Apply Now

Job details

Specified-purpose
€69,614.15–€94,183.85 a year
14 days ago

Qualifications

Analysis skills
Supervising experience
Project management
Bachelor's degree
Quality control
Technical writing
Manufacturing
Communication skills
Negotiation

Full job description

Ireland - Dun Laoghaire

JOB ID: R-244960 LOCATION: Ireland - Dun Laoghaire WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Jul. 15, 2026 CATEGORY: Quality SALARY RANGE: 69,614.15 EUR - 94,183.85 EUR

QC Manager Micro (12 Months)(Specified Purpose Contract)

Amgen, Dun Laoghaire - Dublin

This job operates on a 16/5 cycle shift pattern. This job specification outlines the general responsibilities associated with the role of Manager QC Microbiology on the Amgen Manufacturing site. This role will be responsible for managing the QC Microbiology team and owning, facilitating, and undertaking activities pertaining to Microbiology within QC and Manufacturing. The successful candidate will focus on compliance, continuous improvement and implementing a lean culture and Right First Time (RFT) for QC Microbiology duties and testing, including release of commercial and global release testing. The role also represents the QC unit by liaising with internal and external stake holders.

The site is focused on continuous improvement of all work processes and practices and all colleagues are required to be flexible in this regard. This means that they may be asked to carry out additional work functions that are not described in this specification but are associated with their role. This role will be responsible for oversight of some analytical in-process methods and may require shift work depending on company needs.

Key Responsibilities:

Supervision/Management of QC Microbiology team.
Ensure the QC Microbiology area is operated in a safe manner.
Overall responsibility for QC In process, Environmental Monitoring, Release and Stability testing and the associated test and laboratory documentation.
Develop and maintain quality systems within the QC laboratories to ensure ongoing compliance to cGLP Compliance with Standard Operating Procedures and Registered specifications.
Provide an effective and efficient QC service to operations by supervising, developing and coaching the QC team.
Ensure timely completion of Laboratory Investigation Reports and deviations through the Deviation procedures.
Issue trend reports on investigations, non-conformances and Environmental Monitoring and identify laboratory practices and procedures for further development/improvement.
Keeps abreast of current Corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
Approval of SOP’s, trend data, investigations, non-conformances, validation protocols, reports, method validation/verifications and equipment qualifications.
Participate in regulatory agency inspections as required.
Plan and implement procedures and systems to maximise operating efficiency.
Manage and contribute to the achievements of department productivity and quality goals.

Primary knowledge, skills, competencies and relevant experience Knowledge:

Broad technical knowledge within Microbiology and expanding knowledge of related disciplinary areas Recognizes and understands the cross-dependencies of the role and understands the impacts on the organization Enhances own knowledge through understanding business trends and objectives Knowledge of industry and business principles Understands the core business process and purpose of the functional area in Amgen's commercialization process Developing own project management techniques

Problem Solving:

Applies analytical skills to evaluate and interpret complex situations/ problems using multiple sources of information Creates new procedures and processes to drive desired results Handles diverse scope of issues that require evaluation of a variety of factors including current business trends

Autonomy:

Managerial/Supervisory experience with a proven record in a Supervisor/ Team Lead role Experience leading cross-functional teams is desirable Work is guided by operational and project objectives Manages multiple assignments and processes Independently determines approach to project May be responsible for specific programs and/or projects Independently develops solutions that are thorough, practical, and consistent with functional objectives

Contribution:

Contributes to work group/team by ensuring quality of tasks/services provided by self and others with a strong focus on RFT and Lean Provides training and guidance to others Extends capabilities by working closely with senior staff/experts within and outside the internal organization

Skills:

Lead with initiatives to identify and drive improvements Communication skills (verbal and written) at all levels Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls) Presentation skills Escalate issues professionally and in a timely basis and know when to escalate Decision Making skills – will be require to make decisions independently Teamwork, Coaching and motivating others Negotiation and Influence skills, Planning and organisation skills Investigation skills Demonstrated ability to interact with regulatory agencies Experience working with interdepartmental and cross functional teams and influencing decisions

Relevant experience:

Bachelor’s degree in a Science related field is required. 6+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry, with 2 – 3 years of specific Microbiology management experience desirable. Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products. Some analytical experience for oversight of analytical in-process methods would be an advantage. Possess key competencies to include planning/organisation, problem solving, communication, teamwork, flexibility, coaching and motivating. Proven experience of leading teams.

Apply Now

Refine Your Search

science shift team jobs in dublin, d

Sr Biopharmaceutical Rep-Repatha-Nanning

Manufacturing Technologist

Senior Manager, Operations Supply Planner

Senior Expert (Rapid Prototyping)

Social Care Leader

Senior Principal Developer

Manager, Engineering (Backend Development)

Systems Architect – Connected Medical Devices (Interface Architect)

Manager, Digital Optimization - Campaign Tagging Lead

PM2 Manufacturing Manager (Days)

Defect equipment Systems Engineer

Clinical Development Medical Director - Neuromuscular

Senior Project Manager, GSC Business Performance & Transformation

Global Head of Talent Acquisition

TFSM IR EHS Safety and Industrial Hygiene Engineer

Director, Software Engineering

Global Labelling Director, Content

Senior Manager, Supplier Compliance & Third Party Risk Management (TPRM) – Global Procurement

Senior Manager, Serialization Data Operations

Sr. Director & Head of Architecture

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