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Doc Controller with experience in change controls required for a Biopharmaceutical site based role in Cork. Updating of procedural documents The successful person will be an active member of the team, providing support, guidance and expertise to ensure the success of the department. Responsibilities; Preparation of change control documentation
3 month contract with a view to permanent opportunity for a Document Control Administrator based in East Cork - Your new company - You new company is a engineering supplier of green energy including wind power, providing power to over 300,000 homes across Ireland - Your new role
Experience of control document review and approval. Review and approve validation and control documents as part of the site Quality system. You will have a minimum of 3rd Level Diploma in EHS is required with a minimum of 3 years’ experience in EHSS and/or engineering related positions.
Manage document control, filing and records - Take Operational Controller calls from OEMs - Ireland - Job Description: Operations & Quality Assistant - Location: Cork Airport Business Park, Cork - The Company - Element Power Asset Management (“EPAM”) currently - Manages up to 300MW of Northern Europe wind generation assets from its Control Centre at Cork Ireland.
Contribute directly to the completion of projects through development and execution of validation change control documents, and development and review of protocols, reports and data tables generated by peers and contract personnel
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Our Cork based client currently have an open postion for a Senior Document Controller to join there team on a contract basis. * Administration and support of the relevant electronic document management systems (EDMS) Ø Tracks documents through these processes and gives support to relevant users accordingly.
Contribute directly to the completion of projects through the management of assigned personnel, development and execution of validation change control documents and development and review of protocols, reports and data tables generated by peers and contract personnel - Co-ordinate review of vendor supplied documents including FAT, SAT & IOQ protocols
Provide technical expertise and leadership to the QA group with regard quality systems, document control and lot release - Responsibilities - Recruit, develop and lead the QA team in areas of expertise and high performance team behaviours
Ensure the assigned fund accounting team operates within the clearly defined and documented control environment. The Fund Accounting Manager will be required to manage the overall NAV calculation process within the guidelines and procedures provided, under the supervision and guidance of a Fund Accounting Director and Managing Director.
Ensure the assigned fund accounting team operates within the clearly defined and documented control environment. Opportunity to hire and develop a team around you. Dublin/Cork/Luxembourg or Poland *Opportunity to grow a team around you and be part of a key growth phase for HedgeServ* Company Description - Job Description
Information Developer develops simple standalone documents, or portions of more complex documents. Understanding of document control and revision. Understanding of good documentation practice and effective document structure. Understand the operation of security and fire products and document their operation - Able to format and lay out standard documents
Manage the document control to ensure the all relevant logs are kept up to date at all times - Senior Electrical Engineer required to join one of Ireland's top M&E Contractors based in either Dublin or Cork. Excellent package on offer, scope for career progression and a great place to work. Senior Electrical Engineer
A proven knowledge of GMP procedures and the requirements of change controls, Standard Operating Procedures, document control, etc. Initial 12 month contract. Chemical Process engineers desired, excellent opportunity for a candidate with 1-2 years relevant expeirence. Overview
A proven knowledge of GMP procedures and the requirements of change controls, Standard Operating Procedures, document control, etc. Changeover Specialist required for a leading API facility in Cork. Initially an 11 month contract. The changeover of equipment trains from product to product is a key activity for the site.
Presents finalized procedures in defined formats for document control and diligently verifies files and records for historical purposes. Conducts incident investigations and documents outcomes - Facilities Engineer required for medical device manufacturing facility in Ringaskiddy, Cork. Will manage the facilities EHS and Compliance programs.
Supervision of the development, maintenance, and distribution of quality documents within the Quality Management System, 7 years+ work experience to include specialist experience in a QA or document control role and demonstrated supervisory or management experience. Our client is a highly respected and established medical devices company in the South East.
Processes system change control, documents configuration and writes test plans. Configures the Compliance Wire software to meet end-user needs. Regeneron offers a unique, world-class opportunity for interested candidates. Regeneron has been consistently ranked a "Top Employer" in Science Magazine's rankings for pharmaceutical and biotechnology companies.
Support, Maintain and Develop document control system through - Issuance of Document system reports - Ensuring effective resolution of Document system queries or requests - Internal Planning and Communication & document co-ordination - Management of regulatory documents e.g. requested certs of free sale, apostilled certs
Additionally, the individual processes system change controls, documents and maintains configurations to ensure that the MES remains in a validated state. * Processes system change control, documents configuration, and writes test plans to ensure that the MES remains in a validated state.
Initiates Change Control Documents as required. Summary: Lead is responsible for performing leadership-related activities with their direct reports and performs all tasks necessary within the Materials & Dispensing Technician role to support IOPS manufacturing operations. Regeneron offers a unique, world-class opportunity for interested candidates.
change control documents - corrective/preventative action documents Reviews procedures, policies and other instructional documents relating to quality systems to ensure compliance with company policy and local and international regulatory requirements.
Additionally, the individual processes system change controls, documents and maintains configurations to ensure that the MES remains in a validated state. Processes system change control, documents configuration, and writes test plans to ensure that the MES remains in a validated state.
Activities include the development, maintenance and review of Procedures, CAPA’s, SCAR’s, Change Control, Document Control, Deviations etc. The Quality Systems Engineer is responsible for ensuring the successful implementation and maintenance of Quality Management Systems (QMS) across the organisation.