If you are a current Jazz employee please apply via the Internal Career site.Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in nearly 75 countries. For more information, please visit www.jazzpharma.com and follow @JazzPharma on Twitter. Brief Description:To support and control the management of controlled documents at the KSP facility.To support complaints and supplier management within the QMS.Essential FunctionsKey Responsibilities / AccountabilitiesControl and issue of Issuing of Master DocumentsAllocation of Document numbers and maintenance of QA logs.QualDocs DCG User: creating DCCs, sending out controlled copies to internal/external file holdersCreation, checking and storage of executed batch documentsControlling the GMP Archive area at KSPDealing with DCG email requestsProject support when required.Supplier / Vendor Change ManagementCollating metrics and KPI dataOperates in accordance with the GW corporate values of being patient driven, passionate, innovative, collaborative, accountable, having integrity and achieving excellenceThe job holder is responsible for maintaining cGxP and H&S knowledge applicable to the job.The job holder must refer to the EHSS Policy (EHSS_P.01) to understand the current EHSS responsibilities for the role.Detailed responsibilities / AccountabilitiesControl and Issuing of Master Documents.Logging, issuing, scanning, filing of master documentsAllocation of Document numbers and maintenance of QA logs.Generating new numbers when required and ensuring data is entered accurately.Creation and storage of executed batch documentsCreation of batch documents to Production areas for executionChecking of variable data within batch documents and confirming in NAVArchive of released batches in a timely manner to ensure they are secureQualDocs DCG userCheck of documents (when required) within QualDocs and creating Document Change Control within the system to allow documents to be approved/obsoleted.Identifying any controlled copies to be sent out to external/internal file holdersCreation of execution copies.Maintenance of QualDocs system, ensuring documents are compliant and proceed through their lifecycles.Assisting users when required.Control and maintenance of the GMP Archive area at KSPRetrieving documents from the Document Archive ensuring the control and maintenance of the archive area and checking the contents of all boxes submitted for archiving have been listed accurately.Dealing with DCG email requestsEmails sent to the DCG mailbox are to be actioned accordingly in a timely manner.Project SupportSupporting projects when required.Supplier / Vendor Change ManagementFacilitates management of supplier / vendor change notifications throughout the business to ensure compliance of KSP processes is maintained.Collating metrics and KPI dataWeekly and monthly reporting of KPIs and metrics such as Off-site Archiving, DCC rejections, overdue documents.AdHocCan sign documents (pp) on behalf of another Document Control Senior Coordinator and Document Control Coordinator in times of absence, and where experience allows.To perform duties or projects as required by Line Manager.Carries out their work in a way that will not adversely affect their own, or others, health, safety and security or the environment and reports any shortcomings in GW arrangements.Operates in accordance with the GW corporate values of being patient driven, passionate, innovative, collaborative, accountable, having integrity and achieving excellenceActively looks for improvements in productivity and efficiency within own work areaWorks in accordance with the systems in place with regards to health 'safety, security and the environmentUndertakes other activities, indirectly related or unrelated to the above listed accountabilities, as assigned by line manager/GQLTRequired Knowledge, Skills, and Abilities Skills:Working knowledge of Microsoft Word and Excel.An organised approach to documentation with an eye for detail.Patience, ability to finish tasks and determination to see through tasks to the end.Education to secondary level or above. Ideally with a scientific backgroundGood communication and person management skills are necessary.Knowledge in either GMP or in Quality Systems.Experience of being in Audit situations.Attributes and Behaviors:Proven organisational and interpersonal skills, demonstrated through the following competencies:Customer Focus: Is dedicated to meeting the expectations and requirements of internal and external customers; gets first-hand customer information and uses it for improvements in products and services.Integrity and Trust: Is widely trusted; is seen as a direct, truthful individual; can present the unvarnished truth in an appropriate and helpful manner; doesnt misrepresent him/herself for personal gain.Peer Relationships: Can quickly find common ground and solve problems for the good of all; can solve problems with peers with the minimum of noise; is seen as a team player and is cooperative.Functional/Technical skills: Has the functional and technical knowledge and skills to do the job at a high level of accomplishment.Time Management: Uses his/her time effectively and efficiently: concentrates his/her efforts on the more important priorities: gets more done in less time than others; can attend to a broad range of activities.Action Orientation: Enjoys working hard; is action orientated and full of energy for things he/she sees as challenging; not fearful of acting with a minimum of planning; seizes more opportunities that others.Organising: Can marshal resources (people, funding, material, support) to get things done; can orchestrate multiple activities at once to accomplish a goal; uses resources effectively and efficiently, arranges information and files in a useful manner.Listening: Practices attentive and active listening; has the patience to hear people out; can accurately restate the opinions of others, even when he/she disagrees.Approachability: Is easy to approach and talk to; spends the extra effort to put others at ease: can be warm, pleasant and gracious; is sensitive to and patient with the interpersonal anxieties of others; build rapport well.Informing: Provides the information people need to know to do their jobs and to feel good about being a member of the team, unit, and/or organisation; provides individuals information so that they can make accurate decisions; is timely with information.Required / Preferred Education and LicensesEducation:N/AExperience:Completion of Secondary school education.Typically, minimum of 4+ years relevant work experience in Pharmaceutical, Biotechnology or a related industry Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html.
Job Title
Sr Document Control Coordinator (12 month FTC)