Jobs Químico/a de Controlo de Qualidade - Loures
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Químico/a de Controlo de Qualidade - Loures

Clan

Oferta Full-time
Qualidade Loures €920 - €1 907/mês mercado Posted 6 days ago
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0
Applications
18/04/2026
Há 6 days ago

Description

Detalhes da oferta Descrição: Join a leading , recognized for its innovation, quality, and scientific excellence.

We are hiring Analyst.

If you’re looking to grow your career in an environment that values precision, continuous improvement, and teamwork, this is the perfect opportunity for you!

O que terás de fazer - To organize and define daily priorities within their assigned tasks in order to accurately and promptly perform the allocated sample analysis to meet the requirements of the periodic laboratory plan and area KPIs;

  • To adhere to the laboratory testing - To perform routine calibration and both corrective and preventative maintenance of designated laboratory instruments, requesting any instrument parts and consumables required by the area;
  • Comply with the high standards in the QC Laboratories;
  • To bring any discrepancies, deviations or non-conformance in testing or work practice to the attention of QC management in accordance internal procedures;
  • To issue events and support the investigation of OOS/OOT/atypical results, deviations and QC incidents generated in the QC Laboratories.
  • Ensure appropriate communication with other internal department in relation to QC work by using the appropriate company processes and their IT platforms;
  • Assist with audits as required, following the instruction of QC Management;
  • Undertake any additional tasks to support the laboratory activities as and when required;
  • Seek out additional information when one feels that the available information is not enough;
  • Follow all annual performance review requirements, including completion of the self-assessment;
  • Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health & safety rules/procedures, regulations and codes of practice;
  • Ensure facility activities are carried out in compliance with all GMP, legal and HSE regulations and applicable standards in the country of operation, complying with and enforcing all company processes and good practice.
  • Cumprir normas de segurança e práticas de qualidade em todas as atividades..

O que precisas de garantir - University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar Chemistry, Biochemistry or Health Sciences field (mandatory) - Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field (mandatory);

  • Relevant work experience;
  • Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (mandatory);
  • Experience of GMP practices and HSE standards (preferable);
  • Technical understanding of GMP practices, analytical theory and techniques - Clear and open communication skills (written and verbal);
  • Competent (written and verbal) English (preferable for sites where English is not the first language);
  • Ability and availability to work in shift patterns, as required by business needs;
  • Computer literate with knowledge of the MS Office package AK382;
  • Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down.

O que te proporcionamos - Salary compatible with function.

Responsabilidades

O que terás de fazer - To organize and define daily priorities within their assigned tasks in order to accurately and promptly perform the allocated sample analysis to meet the requirements of the periodic laboratory plan and area KPIs;

  • To adhere to the laboratory testing - To perform routine calibration and both corrective and preventative maintenance of designated laboratory instruments, requesting any instrument parts and consumables required by the area;
  • Comply with the high standards in the QC Laboratories;
  • To bring any discrepancies, deviations or non-conformance in testing or work practice to the attention of QC management in accordance internal procedures;
  • To issue events and support the investigation of OOS/OOT/atypical results, deviations and QC incidents generated in the QC Laboratories.
  • Ensure appropriate communication with other internal department in relation to QC work by using the appropriate company processes and their IT platforms;
  • Assist with audits as required, following the instruction of QC Management;
  • Undertake any additional tasks to support the laboratory activities as and when required;
  • Seek out additional information when one feels that the available information is not enough;
  • Follow all annual performance review requirements, including completion of the self-assessment;
  • Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health & safety rules/procedures, regulations and codes of practice;
  • Ensure facility activities are carried out in compliance with all GMP, legal and HSE regulations and applicable standards in the country of operation, complying with and enforcing all company processes and good practice.
  • Cumprir normas de segurança e práticas de qualidade em todas as atividades..

Requisitos

O que precisas de garantir - University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar Chemistry, Biochemistry or Health Sciences field (mandatory) - Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical-related or other science-related field (mandatory);

  • Relevant work experience;
  • Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (mandatory);
  • Experience of GMP practices and HSE standards (preferable);
  • Technical understanding of GMP practices, analytical theory and techniques - Clear and open communication skills (written and verbal);
  • Competent (written and verbal) English (preferable for sites where English is not the first language);
  • Ability and availability to work in shift patterns, as required by business needs;
  • Computer literate with knowledge of the MS Office package AK382;
  • Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down.

Condições O que te proporcionamos - Salary compatible with function.

Weather on start day

Friday, 24 de April — Partly cloudy · Max 23° · Min 13° · Rain 0% (0mm) · Wind 20 km/h

Previsão para os dias seguintes

  • Sat, 25 Apr
    Partly cloudy
    Max 24° · Min 14°
  • Sun, 26 Apr
    Partly cloudy
    Max 27° · Min 15°
  • Mon, 27 Apr
    Partly cloudy
    Max 28° · Min 18°
  • Tue, 28 Apr
    Partly cloudy
    Max 27° · Min 16°

Detalhes

Listing type
Job Offer
Schedule Type
Full-time
Category
Qualidade
Status
Location
Loures
Start
18/04/2026

Salário de Mercado

€920 - €1 907/mês