Search Results: 296 vacancies
Within this role you will be responsible for managing and overseeing Document Control and Archives operations. This includes oversight of the following: document workflows, records issuance, paper and electronic records archives, inspection support, projects, and metrics....
Within this role you will be responsible for the commercial Manufacturing Documentation team. Facilitate and coordinate Manufacturing records review to meet batch disposition timelines, preparation and review of Cleaning Verification Packs, PRIMR data entry and management of...
...Summary: Provides support to the process for creating, reviewing, approving, distributing, controlling and maintaining documentation to ensure effective and efficient application of GMP.
Documentation within this process includes, but is not limited to, manufacturing and...
...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...
...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...
Job Title: Facilities Maintenance Specialist (CMMS Coordination)
Department: Facilities Maintenance
Summary: Responsible for the administration... ...change controls, creating and updating new and effective documentation to support BMRAM operations via workflows on qualified...
The CMC Regulatory Affairs Specialist is responsible for for a subset of programs at the IOPS facility. Evaluate proposed changes to IOPS documents and procedures to determine regulatory impact.
E ssential Duties and Responsibilities include, but are not limited to, the...
...Document Controller Quality
Kenny-Whelan are hiring a Document Controller Quality for one of its Global Life Sciences Companies in Limerick.
Contact :Carmel Synnott : ****@*****.*** or call on (***) ***-****
Profile of the Role:
Responsible for Electronic...
...Summary:
The Compliance Specialist, Technical Operations is a member of the Technical Operations Team (Automation, Engineering & Facilities... ..., authorship, review, submission, and follow-up/completion of documents such as Change Controls, risk assessments, impact statements...
...The Post Market Surveillance Specialist 1 assists in the implementation of regulatory strategies, performs activities associated with... ...where required, circulation of change requests
Organizing documentation notarization, legalization / apostille with notary, Department...
...Engineering, Automation & Facilities departments.
As a Compliance Specialist in Technical Operations a typical day might include, but is not... ...Reviewing Equipment Drawings, Schematics, Life Cycle Documents, and Automation programming
Reviewing SOPs, Work Instructions...
...involved in technical transfer of processes.
As a Process Specialist-Formulation a typical day might include, but is not limited to... ...reviewing, Standard Operating Procedures and other controlled documents as needed
Providing technical input to resolve process problems...
Summary: The Quality System Specialist participates in maintaining site compliance of operations inclusive of but not limited to Manufacturing... ...for QA review and approval of the following types of documents: Failure investigations / Corrective and preventative actions (...
...of manufacturing deviations and change controls.
As an Associate / Compliance Specialist a typical day might include, but is not limited to, the following:
Coordinating and documenting of manufacturing quality events including but not limited to deviations and change...
About Northern Trust: Northern Trust, a Fortune 500 company, is a globally recognized, award-winning financial institution that has been in continuous operation since 1889.
Northern Trust is proud to provide innovative financial services and guidance to the world’s ...
...this role you will be responsible for supporting the Environmental, Health and Safety for the Limerick IOPS location.
As an EHS Specialist a typical day might include, but is not limited to, the following:
Developing, implementing and monitoring environmental, health...
...standards policies and procedures
A typical day as a QA Validation Specialist, may include:
Generates, executes and/or reviews master and... ..., edits and approves change controls, SOPs, reports and other documentation
Coordinates with other departments or outside contractors/...
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...
...standards, policies and procedures.
As a Principal QA Validation Specialist, a typical day might include, but is not limited to, the... ...editing, and approving change controls, SOPs, reports and other documentation
Coordinating with other departments or outside contractors/...
€50k - €60k per annum
We are seeking a Quality Assurance Specialist to join a pharmaceutical company based in Limerick.
WHAT WE OFFER
* Salary between €50,000... ...advancement.
RESPONSIBILITIES
* Review and approve manufacturing documents, including batch records, standard operating procedures (SOPs),...