Search Results: 358 vacancies
...this role is to ensure regulatory adherence of Cook Medicals
document control process.
Reporting to: Manager, Quality Systems
~•... ...Product Lifecycle Management (PLM) system. • Processing and GMP / GDP review of Change Orders (CO’s). • Ensure Change Orders are implemented...
...Analytical Technologies, IPC lifecycle, Data Analytics, Manufacturing Support, Process Validation and Process Solutions.
As a Temp Data Review Associate you will establish, organize and maintain effective process data co-ordination and data evaluation services.
A typical...
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...
...investigations, etc
Participating in training of other new employees and prioritizes workloads on a daily basis
Performing peer review of data
Performing laboratory investigation reports
Performing microbial identification procedures
Maintaining laboratory supplies...
£ 35 - 60 per hour
...to market.
Responsibilities
Design, prototyping, test design, reviews, evaluations, V&V and protocols
Preparation & presentation of designs... ....
Please click to find out more about our Key Information Documents. Please note that the documents provided contain generic information...
Limerick
3 days ago
...service.
Role:
The Auditor is responsible for conducting and documenting routine audit examinations throughout Northern Trust Corporation... ...in developing testing approach and applies analytical skills to review information and determine potential control weaknesses...
...tasks necessary for the creation and maintenance of quality GMP documentation in support of the Technical Operations Engineering and... ...document control procedures, and good documentation best practices. Review internal
GMP documents to ensure they are compliant with these...
...used in Revenue when generating functional test scenarios.
· Review design specifications and generate test scenarios for either... ...existing test suites.
· Raise defects (Bugs) to development.
· Documenting testing process and results.
· Support Development and Test...
...requirements and regulations.
~Responsible for approving appropriate quality-related documents. An approval signature confirms that the company, GMP and relevant regulatory requirements have been met
~Review and approve change controls, deviations, failure investigations, suspect...
...communications relating to incoming VIG guests via phone & email.
Reviewing the guest history (if available) from previous visits and... ...guests.
Upon departure, you will keep an up-to-date archive of documents, and preferences to enhance the guest's future visits.
Our...
...their specialized field.
Key Responsibilities:
Review functional design specifications.
Write detailed acceptance... ...testing (BPT).
Adher e to Revenue ’ s Test ing processes and documentation standards.
Document testing processes.
Coaching and...
...Analyst within the Biochemistry Lab, a typical day might include, but is not limited to, the following:
Gathers data and documents test results
Reviews test results to ensure compliance with standards; reports any quality anomalies
Complies with all pertinent...
...reducing client operational efficiencies
Lead client service reviews
Administration of client accounts
Maintenance and... ...management of restructure and transition activity
Identify, document, and manage client-related risk issues ensuring adherence to corporate...
Within this role you will support the organization by eliciting and documenting requirements, understanding complex business processes, and... ...a technology to be implemented
Collaborates in the creation, review and approval of validation documents
Recommends business process...
...include, but is not limited to, the following:
Coordination and documentation of QC quality records including but not limited to, Change... ...Control/CAPA events and align team on approach forward
Reviewing, editing, and revising controlled documents ( logbooks, SOPs,...
€56k - €80k per annum
...with the tendering of maintenance contracts as necessary.
~Reviewing reports on regulatory compliance of plant and insurance inspections... ...attending design development meetings, reviewing specification documents and vendor submissions, snagging of services installations,...
...process equipment and manufacturing
Assisting in the design review, site acceptance and installation of equipment
Preparing piping... ...Supporting QA Validation department by preparation of design documents and assisting in protocol execution
Assisting in investigations...
...solutions or recommendations for changes and/or improvements.
Reviews, edits, and approves deviation notifications, deviation... ..., edits, and approves change controls, SOPs, reports and other documentation.
Coordinates with other departments or outside contractors/vendors...
