Quality Control Specialist

Há 1 mês

Lisboa, Lisboa, Portugal Multipessoal Tempo inteiro
Job Summary

We are seeking a highly skilled Quality Control Associate to join our team at Multipessoal. As a Quality Control Associate, you will be responsible for ensuring the quality of our products and processes, working closely with cross-functional teams to identify and resolve analytical problems, and maintaining accurate laboratory records.

Key Responsibilities
  • Apply and develop knowledge of Quality Control principles and procedures.
  • Manage, execute, and support all assigned projects in accordance with GMP, quality operational standards/procedures, and legal regulations.
  • Propose new methodologies considering project demands and requirements.
  • Execute project-specific analytical tasks and act as a stakeholder liaison.
  • Support the induction of new colleagues within the area.
  • Ensure that all assigned analytical tasks are well managed and delivered on time, safely, efficiently, reliably, and in a cost-effective manner.
  • Solve analytical problems relating to assigned projects by providing collaborative and timely support to all areas and departments.
  • Ensure effective and proactive flow of information between the Analytical team and internal and external stakeholders.
  • Review work generated by the team as required, 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, project and general logbooks, and notebooks to an acceptable GLP standard and in accordance with internal procedures.
  • Fulfill and promote all applicable GMP requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities.
  • Advocate for safe operating and high-quality performance, alerting ascending colleagues to any potential risks, discrepancies, deviations, or non-conformance in accordance with internal procedures.
  • Assist with audits/investigations as required, following the instruction of QC Management.
  • Support the reporting of KPIs for the team, if required.
  • 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), among others.
  • Interpret data and analysis to ensure meeting strict guidelines on documentation and recording data.
  • Work collaboratively in cross-functional teams and understand each department's function and role in the delivery of tests and products.
  • Execute professional activities in compliance with GMP and HSE guidelines, internal and external requirements, and promote the implementation and maintenance of systems and procedures (COPs, HBR, SOPs, and others).
  • Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and comply with environmental, health & safety rules/procedures, regulations, and codes of practice.
Requirements
  • University or equivalent qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a similar Chemistry, Biochemistry, or Health Sciences field (mandatory).
  • Requires educational/training experience in a QC laboratory environment.
  • Hands-on experience in Analytical Chemistry and QC procedures (desirable).
  • Training and experience of GMP and ICH guidelines standards (desirable).
  • Knowledge of HPLC and GC, and familiarity with Empower Software (desirable).
  • 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.

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