Search Results: 52 vacancies
...final reports to cGMP standards.
* Generation of validation investigations and implementation of corrective actions.
* Creation, review and approval of various quality documents and test data.
* Management of validation exception events and change control processes....
£ 43 - 56 per hour
...Specifications.
* Selecting Vendors and completing Vendor evaluation matrix.
* Writing RCE's, placing orders, Project Management & Design review meetings.
* Working to the ASME BPE 2019 Standard and relevant ISPE Guidelines etc.
* Coordination of processing equipment...
...hardware problems as required.
* Execute routine system administration and maintenance activities as required (Including system audit trail review, system patching, back-up and restore and system recertification)
* Record all incidents, support issues and changes using the SNOW...
£ 43 - 56 per hour
...Working as part of a large CAPEX Projects team within a start-up GMP facility (greenfield / brownfield).
· Involvement in design, Vendor review, FAT, SAT, I/O/PQ
· Work with project stakeholder team to ensure all process equipment and systems are managed appropriately for the...
...month contract.
The successful individual will conduct quality-related activities such as preparing compliant documents & records; review & approval of quality records, product labels and product specification documents; and will help to support implementation of projects...
...identifying risks, and developing and executing contingency plans.
Ensure compliance with relevant SOPs.
Ensure successful amendment, review and implementation of SOPs changes.
Represent Automation at regulatory and customer inspections and audits.
Qualifications...
...quality system with other personnel where required.
Support Change Management Process including Product and Quality System document review and updates.
Generate and Providing metrics for inclusion in the management review, monthly reports and overall Quality Performance...
...objectives.
Responsible for manufacturing compliance with all safety, environmental and quality related SOPs.
Ensure successfully review, amendment and implementation of changes to SOPs and managing CAPAs.
Promote a culture of perfect performance and Enhanced Right...
...needs and to meet clearly stated objectives.
Responsible for systems compliance with quality related SOP’s.
Ensure successfully review, amendment and implementation of changes to SOP’s.
Need to front audits by HPRA/FDA or Customers on Control Systems.
Qualifications...
...complies with GMP and Regulatory standards. Responsibilities include validating facility, equipment, and utilities, as well as reviewing and approving validation documentation . This individual contributor role requires a self-starter with expertise in QA and validation...
....
Dedicated team and access to a knowledgeable Multidisciplinary team.
The above job description is intended to be neither definitive nor restrictive and the duties and responsibilities and purpose of the post may change and may be subject to periodic review....
...reports.
Project engineering submissions and value engineering.
Project procurement and materials management.
Project build review and interaction with co-contractors.
Designing in 3D using AutoCAD 3D software.
Evaluating final product's overall performance,...
...Professional / Clinical
The Clinical Nurse Manager 1 will:
• Be responsible for the co-ordination, assessment, planning, implementation and review of care for service users according to service standards.
• Provide safe, comprehensive nursing care to service users within the...
...Laboratory
~ Data Integrity.
~Ensuring all lab equipment is calibrated and maintained, adhering to calibration
~ schedules.
~Review of documentation, pre and post approvals.
~ Liaising and working with external vendors.
~ Management of the Maximo system, ensuring...
€45k - €50k per annum
...salary and benefits package
Excellent opportunities for career progression and advancement.
Key Responsibilities include:
Quality review of process validation plan, protocols, and reports.
Co-ordinate and contribute to the generation and maintenance of compliant...
...and final reports to cGMP standards.
Generation of validation investigations and implementation of corrective actions.
Creation, review and approval of various quality documents and test data.
Management of validation exception events and change control processes....
€50k - €60k per annum
...technical expertise on QA and compliance topics.
Manage assigned areas of the Quality Management System (QMS) for GMP compliance.
Review and approve validation documentation related to facility, equipment, and utilities.
Contribute to technology transfers and new...
...experience in Engineering.
~ Project planning and execution.
~ Testing and investigation of product issues.
~ Technical input and review of complaints.
~ Good mental ability to logically follow a line of though for problem solving.
For a confidential discussion...
...Project scheduling, progress reporting and resource deployment.
Project procurement and materials management.
Project build review and interaction with co-contractors.
Project commercial management, cost control and cost recovery for contract and variation works...
...across internal departments.
Continually coaching team to ensure that product knowledge, company policies and our brand values are reviewed and reconsidered at all times.
People management activities, working in liaison with HR & senior management.
Completing regular...