Search Results: 439 vacancies
...The primary function of this role is to ensure regulatory adherence of Cook Medicals
document control process.
Reporting to: Manager, Quality Systems
~• Change Analyst within the Agile Product Lifecycle Management (PLM) system. • Processing and GMP / GDP review of...
QA Specialist
This role participates in maintaining site compliance of operations inclusive of but not limited to Manufacturing, Quality... ...Responsible for review and approval of the following types of documents: - Failure investigations - CAPA - SOP’s - GxP documents - Change...
...operational processes. With a footprint across North America and Europe, the company carefully automates and services R&D, production, packaging, and delivery processes—globally—with a sophisticated blend of products, technologies, and lifecycle services.
Catalyx is a...
...deliverables are being met.
Job Purpose:
The Specialist is a member of a team within Quality and is... ...Review and approve production and analytical documentation accompanying the release of drug substance, drug product and packaged finished goods to ensure conformance to...
...Document Controller
Kenny-Whelan are hiring a Document Controller for one of its Global Life Sciences Companies in Limerick.
Contact :Carmel Synnott : ****@*****.*** or call on (***) ***-****
Profile of the Role:
Responsible for Electronic Documentation...
...Our client is looking for a full time permanent Payroll Specialist to join their Limerick team. The successful candidate will also be... ...quarterly excess & obsolesce file
Completion of quarterly tax package.
Other Ad-hoc duties, projects or assignments as needed or directed...
...that means business
Who we are:
Sustainability software specialist, AMCS, is headquartered in Ireland, with offices in Europe,... ...procedures, along with experience of producing and maintaining SOP documentation.
~ A natural curiosity to challenge status quo and willing...
...company in the heart of Tipperary, is seeking a Quality Systems Specialist to join our ambitious team. We are committed to improving... ...Provide support to Non-Conformance, CAPA, Change Controls and Documentation Control activities as required.
Participate in cross-functional...
...timelines for our deliverables are being met.
Associate Quality Specialist supports day to day QA activities in the facility.... ...Laboratory Out of Specification (OOS) and process deviations are documented, assessed and associated CAPA identified.
· Provide support...
CLEANING VALIDATION SPECIALIST with rinse & swab experience required by CareerWise Recruitment for our multinational BioTech client in Limerick... ...protocols, experience on writing and approving Deviations/ GMP documents and Technical writing experience in writing site reports.
Role...
A Cleaning Validation Specialist is required by Careerwise recruitment to work with our Limerick based Biotechnology client.
Role of... ..., edits and approves change controls, SOPs, reports and other documentation.
JOB REQUIREMENTS
BS/BA in Engineering, Chemistry, or Life...
...8788240 for more information.
Environmental, Health & Safety Specialist
24/05/24 Tipperary Neg
Permanent full-time
We have an excellent... ...review of risk assessments.
~Ensure that all incidents are documented, investigated and recommended improvements implemented.
~Responsible...
Additional Locations: N/A
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling...
...Regulatory Strategy & Sustainability.
The Technical Regulatory Specialist supports both the Regulatory Change Oversight and Regulatory... ...review and challenge
Provides clear guidance and documentation to Asset Servicing stakeholders around initial applicability and...
...specific compliance and legal requirements related to interactions with Healthcare Professionals, and prepare and submit relevant documentation to the appropriate functions / departments in accordance with them.
Travel to events to provide on-site event support and execution...
A Compliance Specialist is required by Careerwise recruitment to work with our Limerick based biotech client…12-month contract position.... ...initiation, authorship, review, submission, and follow-up/completion of documents such as Change Controls, risk assessments, impact statements...
...opportunity to join the team as a Quality Assurance Specialist to help us perform a range of chemical, microbiological, sensory and packaging analysis, and ensure that every product... ..., packaging and sensory analysis as documented in the quality plans.
You'll be accountable...
...The primary responsibility of the Supply Chain Operations Specialist is to liaise with internal and external contacts to facilitate the timely supply of finished goods to the end customer. The role is also responsible for monitoring and analysing many areas of the supply chain...
...to clinical trial managers, CROs, and investigator sites.
~ Provides support in reviewing, tracking and/or archiving IP returns documentation.
~ Monitors IP expiry data and informs Clinical Supply team and Clinical Trial teams of pending IP expiry.
~ Facilitates ancillary...
...WestRock (NYSE :WRK) is a global leader in sustainable paper and packaging solutions. We are materials scientists, packaging designers,... ...quality team for auditing supply base
To raise quality documentation as appropriate to release to the supply base
To be proactive...