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Search Results for Biopharmaceutical
Job Title. Location Salary Actions

IPC Analyst

We’re currently recruiting for an exciting opportunity with an award-winning biopharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties • Achieves competency in laboratory methods and procedures. • Trains other QC analysts in laboratory methods and procedureswhen required. • Performs analytical testing activities in relation to methodvalidation and technical transfer activities to ens...

Location: Cork,
IPC Analyst
Cork Not Disclosed

Sr Associate QC Bioassay

We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties •Experience in a wide variety of analytical techniques including but not limited to cell based- Bioassays, Immunoassays, Cell Culture (use of cells to execute bioassays) and Aseptic Technique. Experience with liquid-handling robots is also preferable. • Plan and perform multiple, c...

Location: Dublin,
Sr Associate QC Bioassay
Dublin Not Disclosed

Quality Compliance Specialist

A Quality Compliance Specialist QRM is required to join a leading global biopharmaceutical organisation in Limerick. This role supports the work of our client’s Industrial Operations and Product Supply (IOPS) site through the use of quality risk management (QRM) principles and techniques. The scope may also include collaboration with other IOPS Sites, partners, CMOs and their respective programs. The Role Ensuring compliance with all aspects of the QRM program Provide advice on all QRM matters within the IOPS organization Facilitate risk assessments Res...

Location: Limerick,
Quality Compliance Specialist
Limerick Not Disclosed

Associate Director Quality Risk Management System

Associate Director Quality Risk Management System Our client, a leading biotech organisation are currently recruiting for an Associate Director Quality Risk Management System. As Associate Director Quality Risk Management System you will be global process owner of the end to end Global Quality Risk Management System across global functions at sites, including combination product development, Drug substance and drug product clinical and commercial production. You will be responsible for ensuring adoption of Risk Management principals is applied across disciplines and lifecycle throu...

Location: Limerick,
Associate Director Quality Risk Management System
Limerick Not Disclosed

Technical Writer Senior Associate

A Senior Associate Technical writer – Supply Chain is required to join a leading global Biopharmaceutical business in Dublin. The role will be responsible for leading, coordinating, contributing to and undertaking activities pertaining to Supply Chain Deviations, Corrective/Preventive Actions and Change Controls. The role will provide technical expertise with a focus on Compliance and Continuous Improvement while implementing a Lean Culture and Right First Time (RFT). The role also represents the Supply Chain unit by liaising with internal and external customers. Prim...

Location: Dublin,
Technical Writer Senior Associate
Dublin Not Disclosed

QA Director, Europe

The QA Director, Europe will be responsible for ensuring the company’s GMP and GDP processes and systems are in place to meet or exceed the European Regulatory Authorities’ requirements. Responsibilities: Act as the Responsible / Qualified Person for the local business, ensuring the required cGMP and cGDP licenses are secured and maintained. Lead the local QA team, providing direction and development. Ensure that Health Authority Inspections are appropriately led and managed, as well as other needs and interactions with the relevant bodies. Implem...

Location: Dublin,
QA Director, Europe
Dublin Not Disclosed

Senior GMP Auditor

Consistently ranked as a “Top Employer” in Science Magazine’s rankings for pharmaceutical and biotechnology companies, our client offers a unique, world-class opportunity for interested candidates. An outstanding Senior GMP Auditor is required who is excited by a start-up environment and recognizes the opportunities that this offers and wants to be challenged Summary:Responsible for planning and conducting quality audits in manufacturing (GMP) within designated Quality Auditing area. Responsibilities Schedules, prepares, an...

Location: Limerick,
Senior GMP Auditor
Limerick Not Disclosed

Lab Technician

We’re currently recruiting for an exciting opportunity with an award-winning medical device organization based in Galway. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties You will be part of a high performing Complaint Handling and Medical Device Regulatory reporting department, which provides value throughout the Product Life cycle through world class execution in Medical Device Reporting and Vigilance compliance. Responsibilities may include the follow...

Location: Galway,
Lab Technician
Galway Not Disclosed

Technical Writer

We’re currently recruiting for an exciting opportunity with an award-winning medical device organization based in Limerick . This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties Position Description and Responsibilities Perform technical writing, research, and related editing functions to prepare documents, test plans, user cases, project manuals, business proposals, reports, briefings, presentations, guidelines, and other written materials. Technical Pr...

Location: Limerick,
Technical Writer
Limerick Not Disclosed

Technical Writer Senior

We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties Develop, review and update engineering, manufacturing, & inspection Standard Operating Procedures. Liaise with Manufacturing/Inspection/Engineering regarding documentation changes in an effective and timely manner. Develop protocols for execution...

Location: Dublin,
Technical Writer Senior
Dublin Not Disclosed

QA Specialist - Packaging

We’re currently recruiting for an exciting opportunity with an award winning pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties • Performs a wide variety of activities to ensure compliance with applicable regulatory requirements through support of Packaging and Engineering functions. • Works directly with Packaging and Engineering functions to ensure that inspections, statistical process control analyses and ...

Location: Cork,
QA Specialist - Packaging
Cork Not Disclosed

Application Support Specialist (Chromatography)

Our client is a well-respected & established Irish organisation based in Dublin. They are recruiting for a Chromatography Application Support Specialist to support & deliver solutions to customer applications. This is a collaborative role working within the Sales & Service areas, with the key objective of supporting ongoing development and growth of Chromatography and Mass Spec Solutions. This role will be based in the Munster or Leinster area with a requirement to travel nationwide. Role/Responsibilities: • Support Sales/Service Team in the con...

Location: Dublin,
Application Support Specialist (Chromatography)
Dublin Not Disclosed

QA Validation Manager

QA Validation Manager Our client, a large biopharmaceutical organisation are currently recruiting for a QA Validation Manager to join their team on a permanent basis. As QA Validation Manager you will be responsible for implementing policies and procedures to validate/qualify equipment, systems, and processes in accordance with regulatory requirements and the organisations manufacturing standards, and will manager a team of Validation Specialists. Responsibilities • Manage, develop and build a team of subject matter experts in the areas of cleaning validation and...

Location: Limerick,
QA Validation Manager
Limerick Not Disclosed

Senior GMP Auditor

Consistently ranked as a “Top Employer” in Science Magazine’s rankings for pharmaceutical and biotechnology companies, our client offers a unique, world-class opportunity for interested candidates. An outstanding Senior GMP Auditor is required who is excited by a start-up environment and recognizes the opportunities that this offers and wants to be challenged Summary:Responsible for planning and conducting quality audits in manufacturing (GMP) within designated Quality Auditing area. Responsibilities Schedules, prepares, an...

Location: Limerick,
Senior GMP Auditor
Limerick Not Disclosed

QA Specialist

We’re currently recruiting for an exciting opportunity with an award winning Biopharmaceutical organization based in Cork. This is an excellent opportunit

Location: Cork,
QA Specialist
Cork Not Disclosed

QA Specialist

We’re currently recruiting for an exciting opportunity with an award winning Biopharmaceutical organization based in Cork. This is an excellent opportunit

Location: Cork,
QA Specialist
Cork Not Disclosed

QA Specialist

We’re currently recruiting for an exciting opportunity with an award winning Biopharmaceutical organization based in Dublin. This is an excellent opportun

Location: Dublin,
QA Specialist
Dublin Not Disclosed

Quality Assurance and Regulatory Affairs Manager

Quality Assurance and Regulatory Affairs Manager Our client, one of the largest biomedical innovator based in Dublin is looking to recruit QA/RA Manager wh

Location: Dublin North,
Quality Assurance and Regulatory Affairs Manager
Dublin North Not Disclosed

Consultant

Life Science Recruitment is a specialist recruitment agency with a focus on the recruitment and selection of professionals for the pharmaceutical, biotechnology

Location: Cork,
Consultant
Cork Not Disclosed

QC Lab Analyst

QC Lab Analyst Our Client, One of the Global pharmaceutical companies based in Sligo is currently sourcing for QC Lab Analyst . Thesuccessful candidate willensure that all raw material, in-process and finished product testing and method transfer testing is carried out per schedule and records are maintained to appropriate requirements. Working, in thequality control labs, the successful candidate will be equipped with the latest design technology for chemical and microbiological analytical testing to meet customers’ needs. The R...

Location: Sligo,
QC Lab Analyst
Sligo Not Disclosed

Mechanical Design Engineer

Mechanical Design Engineer required to focus on the development of cutting edge medical devices in the Cardiac and Vascular space. Engineers are directly involved in the development of innovative products for use in medical procedures. Principal R&D Engineers are directly involved in all stages of the product development process from concept generation through to commercialization of cutting edge devices such as structural heart devices. Responsibilities: Support basic clinical need through opportunity assessment and device concept to prototype. You will participate in...

Location: Galway,
Mechanical Design Engineer
Galway Not Disclosed

QA Specialist (QC)

This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities at Janssen Biologics as required by Good Manufacturing Practice (GMP). These activities include Incoming material release, Batch release, Change control, Event management, Supplier qualification, Annual product review and Validation compliance activities.Provide support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met. GENERAL SCOPE OF RESPONSIBILIT...

Location: Cork,
QA Specialist (QC)
Cork Not Disclosed

Senior R&D QA Executive

Senior R&D QA Executive Our client, one of the largest multinational companies based in Galway is recruiting for Senior R&D QA Executive. The suitable candidate must have prior experience working in Aseptic sterile pharmaceutical manufacturing environment with QA/QC with good knowledge of product development. The Position • This position is responsible for carrying out tasks and projects related to managing compliance activities during qualification and validation based on Good Manufacturing Practice (GMP). • These activities include re...

Location: Galway,
Senior R&D QA Executive
Galway Not Disclosed