Lead Analytical Data Reviewer

2 meses atrás


Lisboa, Lisboa, Portugal Multipessoal Tempo inteiro
Job Title: Associate Analytical Data Reviewer

We are seeking a highly skilled Associate Analytical Data Reviewer to join our team at Multipessoal. As a key member of our QC laboratory, you will be responsible for ensuring the quality and accuracy of analytical data in the pharmaceutical industry.



Main Responsibilities


  • Manage, execute and support projects in accordance with GMP, quality operational standards, and legal regulations.
  • Propose new methodologies considering project demands and requirements.
  • Execute project-specific analytical tasks and act as a liaison with stakeholders.
  • Ensure all assigned analytical tasks are well managed and delivered on time.
  • Solve analytical problems by providing collaborative and timely support.
  • Ensure effective information flow between the Analytical team and stakeholders.
  • Review work generated by the team, ensuring all procedures are followed.
  • Create, investigate, and evaluate CAPAs, incidents, and deviations.
  • Perform equipment maintenance, internal calibrations, and internal qualifications on designated laboratory instruments.
  • Accurately use and maintain all laboratory information systems.
  • Maintain good hygiene and housekeeping within the laboratory.
  • Maintain all laboratory records to an acceptable GLP standard.
  • Fulfil and promote all applicable GMP requirements and HSE regulations.
  • Support the reporting of KPIs for the team.
  • Develop and accumulate strong analytical chemistry expertise.
  • Maintain high standards in the QC Laboratories.
  • Use analytical techniques and instrumentation, such as gas and high-performance liquid chromatography (HPLC).
  • Interpret data and analysis to ensure strict guidelines on documentation and recording data are met.
  • Work collaboratively in cross-functional teams.
  • Execute professional activities in compliance with GMP and HSE guidelines.
  • Carry out assigned tasks in a safe manner, in accordance with instructions.


Requirements


  • University or equivalent qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or similar field (mandatory).
  • Educational/training experience in a QC laboratory environment.
  • Hands-on experience in Analytical Chemistry and QC procedures.
  • Training and experience of GMP and ICH guidelines standards.
  • Knowledge on HPLC and GC, and familiarity with Empower Software.
  • Technical understanding of GMP practices, analytical theory, and techniques.
  • Documentation skills and attention to detail – Fluency in English is a requirement.
  • Computer literate with good working knowledge of the MS Office package.


Join our team and contribute to the success of Multipessoal



Contact Information



Please apply through our website or contact our HR department for more information.



Original Language: en



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