Documentation SpecialistResponsibilities:Responsibility for the timely, accurate, and efficient management of documents including access and revision control.Manage “Live” Documentation updates from the Operations floorTurnaround and issue documentation as per Operations ScheduleManage and implement on the floor documentation control systemDrive the Documentation Life Cycle System to ensure documents are approved in as per Scheduling requirements.Work with various Subject Matter Experts to ensure technical documentation updates are approved.Creation and revision of Standard Operating Procedures (SOPs) Work Instructions (WI’s) as requiredWork closely with QA, Supply chain and Operations core functionsEnsure compliance with all regulatory GMP, Safety and Environmental requirements.

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RESPONSIBILITIES:*Consolidation and validation of Project Plans and deliverables.*Co-ordination of effective resourcing of projects and the management of individual performances to defined objectives.*Provision of clearly defined responsibilities and objectives for each project team member*Manage the day to day deliverables of the Project teams*Work with the project team members on a continuous basis to ensure objectives are met or exceeded*Consolidate and communicate project status updates as per stakeholder expectations*Manage communication and work commitments with teams’ external to the core team.*Coordinate project meetings, manage attendance, and ensure defined behavioral norms are sustained.*Facilitate issue resolution through strong and consistent leadership and the application of leadership tools such as the ACM.*Facilitate technical problem resolution through the application of best practice tools such as 8-D, DMAIC, etc.*Ensure that all changes and activities conform to local and corporate, statutory, legislative, and regulatory requirements for GMP, HSE, and Quality.*Provide continuous support and mentoring to the core team members.*Create and maintain an environment of innovative continuous improvement, focusing on quality, cost reduction, process development, and supply.

Documentation SpecialistResponsibilities:Responsibility for the timely, accurate, and efficient management of documents including access and revision control.Manage “Live” Documentation updates from the Operations floorTurnaround and issue documentation as per Operations ScheduleManage and implement on the floor documentation control systemDrive the Documentation Life Cycle System to ensure documents are approved in as per Scheduling requirements.Work with various Subject Matter Experts to ensure technical documentation updates are approved.Creation and revision of Standard Operating Procedures (SOPs) Work Instructions (WI’s) as requiredWork closely with QA, Supply chain and Operations core functionsEnsure compliance with all regulatory GMP, Safety and Environmental requirements.

Job Title Promotions Analyst Location Maidenhead UK Reporting to Regional Promotions Analyst Position Description Summary The Consumer EAME Centre of Excellence has responsibility for providing accounting services, business analytics and reporting for Finance and other functions in 25 countries across the Consumer EAME region. The company Consumer EAME has sales of over $4 bn. & sells approximately 100 different brands. This role is a key part of the EAME Commercial Accounting team, which is responsible for accurate accounting and reporting of sales and customer spend waterfall (gross sales to net trade sales) of the countries serviced by the COE. Key Responsibilities Process responsibilities: • Accurately input, monitor and reconcile promotion conditions for the local markets, according to the appropriate market conditions. • Accurately process claims through the SAP Rebate system. • Communicate and follow up on issues identified, working with stakeholders through to resolution. • Proactively support Finance colleagues in local markets on topics under his / her responsibility. • Suggest, lead and participate in process improvement projects within the commercial accounting team and other teams within the CoE. • Participate in team discussions regarding standardisation of processes across the region and take an active role in pursuing these goals. • Relationship building with local market finance and sales teams will be a key part of this role. • SOX/ Audit Ensure compliance with relevant internal controls and standard operating procedures in order Assist with the requirements of internal and external auditors Compliance Statement: • Ensure strong internal controls are in place, in order to achieve “adequate” internal and external audit ratings. • Accurate and timely month-end reporting. Meet all corporate and regional deadlines.

PE Global are currently recruiting for a QC Lims Administrator for our client site in West Dublin:Duties:*The QC gLIMS Administrator will be responsible for coordinating, facilitating, and undertaking activities pertaining to the Thermo Fisher Sample Manager LIMS system (gLIMS). The QC gLIMS Administrator will build, develop, and maintain LIMS templates and be involved in troubleshooting as required. This role will support The Quality Control team.Skills: *The building, testing, verifying, transferring, reviewing, and activation of all data required for Master Data Load in gLIMS. *Identify area end-user requirements and enhancements to assist with Master Data Load in gLIMS. *Ensure the system master data is updated in a timely manner as required by the area. *Assist in validation (IQ, OQ, PQ) as required *Author/review of validation protocols and reports to ensure compliance with current regulatory expectations.*Investigation of deviations and raising of change controls as required.

Responsible for supporting activities that initiate and maintain international product approvals for Wave 2b and 3 countries.• Partnering closely with other members of the Strategy Implementation Group, Dossier Excellence, Regional Portfolio Leads and Regulatory Operations teams.• Provides support for Wave 2b and 3 market registrations and license renewals.• Providing documentation to support international registration and tender requests.• Prepares responses to questions and requests from health authorities for product registrations.• Managing a significant amount of proprietary information in a confidential manner to prevent loss of intellectual property.• Ensures compliance with regulatory agency regulations and interpretations• Provides solutions to a variety of problems of moderate scope of complexity.• Maintains and archives all regulatory documentation.

RESPONSIBILITIES:*Consolidation and validation of Project Plans and deliverables.*Co-ordination of effective resourcing of projects and the management of individual performances to defined objectives.*Provision of clearly defined responsibilities and objectives for each project team member*Manage the day to day deliverables of the Project teams*Work with the project team members on a continuous basis to ensure objectives are met or exceeded*Consolidate and communicate project status updates as per stakeholder expectations*Manage communication and work commitments with teams’ external to the core team.*Coordinate project meetings, manage attendance, and ensure defined behavioral norms are sustained.*Facilitate issue resolution through strong and consistent leadership and the application of leadership tools such as the ACM.*Facilitate technical problem resolution through the application of best practice tools such as 8-D, DMAIC, etc.*Ensure that all changes and activities conform to local and corporate, statutory, legislative, and regulatory requirements for GMP, HSE, and Quality.*Provide continuous support and mentoring to the core team members.*Create and maintain an environment of innovative continuous improvement, focusing on quality, cost reduction, process development, and supply.

Job DescriptionWe have a fantastic opportunity for a Bio-analytical Method Development & Validation Manager to join our team in Dungarvan Co Waterford. Full time.The purpose of this job is in ensuring appropriate systems & controls are implemented to facilitate the growth of the section and the needs of the business. With the new extension of the Bio-analytical Department at the Dungarvan site this job is to continue to develop the work scope of the dept to facilitate the rapid growth. ResponsibilitiesTo effectively co-ordinate & manage the section so that the quality of the work & the service consistently meet the requirements of the organisation & the client. To effectively manage client project planning, set up & resources.To build & manage client relationships at an operational level. This will include communicating proposals, quotes, operational matters, change orders & delivery of final product. .To ensure equipment & systems calibration / qualification schedules are adhered to.To ensure investigations & technical issues are completed & resolved in a timely manner.For maintaining the MOS (management Operating System) & reporting performance as required.Take responsibility & a hands on approach to achieving the financial targets of the section. To track & control section budget & spending.To collaborate with the other functions / departments as required to ensure that the efficiency & quality of work meets with organisational & client needs.Hire, motivate, develop & retain excellent analysts, scientists & team leaders that fit within the Company culture.To motivate the team to perform to a consistently high standard through staff training & development & continuous feedback on performance. Instill a culture of continuous improvement.Define, agree & track goals & milestones with senior management for the the business unit.To assist in the planning of other resourcesLead according to the Leadership Charter & act as a role model for leadership

Duties-*Cutting and deboning: mutton, pork or beef - for butchers*Working on a slaughtering line: mutton, pork or beef - for slaughters