Jazz Pharmaceuticals
Jazz Pharmaceuticals is a global biopharma 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, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.

Job Description
Brief Description
To analyse and report on QC test samples (e.g. packaging items, raw materials, intermediates, finished products and stability samples) in accordance with cGMP.

Essential Functions/Responsibilities

• Perform analytical testing using HPLC, GC, TLC, FTIR, UV and other required techniques in accordance with written procedures
• Provide clear and accurate records of all work performed
• Record data into appropriate records and notify management of any OOS, OOT, OOE or questionable results
• Ensures that all results are reported and approved in a timely manner
• Identifies any non-compliances or deviations and notifies management
• Carries out checking of analytical documentation (where experience and training allows)
• Ensures that all equipment is fully calibrated and serviced prior to testing
• Applies appropriate SOPs and test methods to all testing to ensure compliance and quality of resulting data
• Authoring, reviewing and approving SOPs, protocols, reports and other related documents
• Leading and documenting investigations, identifying the root causes of problems and introducing effective corrective and preventative actions
• Completion of deviations, change controls, CAPA and other QMS documents
• Carries out training of other staff when required/appropriate
• Maintains a clean and tidy work environment, including carrying out housekeeping tasks as assigned
• Maintains stocks of consumables, chemicals, solvents, etc through regular stock checks and re-ordering when required
• Assists with sampling of raw material samples as required
• Actively looks for and implements improvements in productivity and efficiency within own work area
• Works in accordance with the systems in place with regards to health & safety, security and the environment
• Undertakes other activities, indirectly related or unrelated to the above listed accountabilities, as assigned by line manager
• Can sign documents (“pp”) on behalf of other QC personnel (scientists and below) in time of absence, and where experience allows
• Operates in accordance with the company corporate values of being patient driven, passionate, innovative, collaborative, accountable, having integrity and achieving excellence

Required Knowledge, Skills, and Abilities

• Typically >3 years relevant post degree work experience, ideally in the Pharmaceutical, Biotechnology or a related industry
• Knowledge and understanding of cGMP regulations, in particular those relating to laboratory instruments, equipment, and computerised systems
• Experience of using routine analytical instruments (e.g. HPLC, GC, TLC, FTIR, UV etc.) and of routine analytical techniques (titration, pipetting, etc)
• Practical knowledge of the use, maintenance, and troubleshooting of analytical instruments (including HPLC and GC)
• Experience of Pharmacopoeial testing and/or the use of Pharmacopoeias
• Knowledge and experience of LIMS systems (e.g. SampleManager)
• Knowledge and experience of chromatography data systems (e.g. Empower)
• Working knowledge of office IT packages
• Good level of written and verbal communication skills
• Interpersonal skills and professional skills to interact at all levels including managers, contractors, and colleagues
• Excellent attention to detail and ‘concern for quality’

Required/Preferred Education and Licenses

• Bachelor’s degree in science or related discipline
• Post-graduate qualifications (Master’s, PhD) highly regarded

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