Were currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Waterford.
This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do Main responsibilities: Provide analytical chemistry services and support to Site Effective interaction with other departments on matters related to raw materials, intermediates and finished batch releases.
In particular, close contact maintained with Quality Assurance Production, Engineering and Planners Maintain, update and issue chemical methods, specifications and SOPs in compliance to pharmacopoeial and regulatory requirements Assist with training of the analysts in areas of expertise and knowledge and in new methods, SOPs and updates Trend such results, record on COAs where required and complete OOSs investigations on a timely basis Update the QC Team Leader on potential problems and highlight improvements where possible by use of the normal communication means Audit and review chemistry test results on a daily basis and ensure compliance with cGLP; checking/auditing laboratory notebooks and analytical reports Experience: Relevant laboratory experience obtained in a manufacturing environment Technical and Soft skills: Operational experience of quality laboratories in a fast-moving manufacturing environment Knowledge of quality management systems, pharmaceutical manufacturing operations, requirements for cGLP, pharmacopoeial methods and stability Knowledge of any of the following methodologies: HPLC, ICIEF, CE-SDS Understand relevant quality/compliance regulations, and KPIs for the site Can manage projects to plan/budget Good communication and an effective facilitator Shows flexibility, drive, innovation, can collaborate effectively with others Education: Degree in Science (Chemistry or Biochemistry preferred) If interested in this posting, please feel free to contact Jack Caffrey at or for further information.
Skills: Batch Release Chemistry QC Sterile GMP HPLC