Coordinator, Quality Assurance

Hikma Pharmaceuticals

Sintra

Presencial

EUR 30 000 - 45 000

Tempo integral

14 dias+

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Vantagens oferecidas por esta oferta de emprego

Direct contract with Hikma
Health Insurance
Life Insurance
Annual Performance Bonus

Resumo da oferta

Hikma Pharmaceuticals in Portugal is seeking a Coordinator, Quality Assurance to join the on-site QA team. You will conduct or verify sample analyses, assist with in-process controls, and support aseptic practices and cleaning monitoring.

The role requires attention to detail, ability to work under pressure, and fluency in English. Responsibilities include training new QA analysts, approving maintenance requisitions, sampling finished products, and ensuring compliance with cGMP and regulatory

Qualificações

  • Academic background in science or related field.
  • Ability to multitask and meet tight deadlines.
  • Proactive, detail oriented and flexible.
  • Fluent in English and proficient computer skills.
  • Knowledge of regulatory expectations (cGMP, FDA) for injectables.

Responsabilidades

  • Conducting or verifying analysis of bulksample.
  • Verifying or conducting sampling and analysis during filling.
  • Conducting or verifying analysis after cleaning of machine parts.
  • Sample finished product for testing by Microbiology and QC.
  • Performs round checks in production areas and inspections as needed.
  • Start-up activities before or during production.
  • Perform aseptic practices and cleaning/disinfection monitoring.
  • Accept/verify procedures and defects in production phases.
  • Approve maintenance requisitions for release of production.
  • Train new QA analysts.
  • Verify prints from equipment related to production.

Conhecimentos

Multi-tasking
Attention to detail
English fluency
Strong computer skills

Formação académica

Science degree

Ferramentas

cGMP knowledge

Descrição da oferta de emprego

Coordinator, Quality Assurance

Data: 23/07/2026

Founded by Samih Darwazah over 40 years ago in Jordan, Hikma's purpose is to provide affordable, quality medicines to the people who are competent. Based on very solid foundations, we continue to innovate daily and find practical solutions to transform the lives of the millions of people we serve.

At the end of the 1980s, we extended ours beyond the Middle East and acquired land in Portugal for the construction of a sterile factory for injectable pharmaceutical products. This was an important turning point for the company, and our first step into a new region. Today, in Portugal, we have more than 900 employees and 3 factories for the production of injectable medicines.

Hikma, intends to recruit an Analyst, Quality Assurance(m/f) to integrateQuality AssuranceDepartment,on-site work.

Main Responsibilities:

  • Conducting or verifyinganalysis of bulksample;
  • Verifyingor conducting sampling and analysis of the in-process control during filling of thebatches;
  • Conducting or verifyinganalysis after cleaning of machine production parts to verify cleanconformity;
  • Sample finished product to be tested by the Microbiology and Quality ControlDepartments;
  • Performs round checks in production departments, bulk packaging andinfrastructures;
  • Performs inspections in the production areas whenevernecessary;
  • Carries out the start-up before the beginning or during production (whenever necessary);
  • PerformsAseptic Practices and Cleaning/DisinfectionMonitoring;
  • Samples and carries out acceptance procedures in all the different phases of the production, undertakes visual inspection by attributes fordefects;
  • Approves maintenance requisitions for the release ofproduction;
  • Trains new QAanalysts;
  • Verifiesprint-outsfrom equipment relatedwithproduction activities.

Profile:

  • Academic degree in Science;
  • Ability to handle a multi-task operation, to meet tight deadlines and to work under pressure;
  • Should be assertive, flexible, and attentive to detail;
  • Fluency in English and good computer skills are preferred;
  • Knowledge regarding the Injectables pharmaceutical industry, current Good Manufacturing Practices (cGMPs), Food and Drug Administration (FDA) and other regulatory authority requirements;
  • Availability to work 8-hour shifts;
  • Own vehicle required.

We offer:

  • Direct contract with Hikma;
  • Competitive salary aligned with the role;
  • Life insurance;
  • Health Insurance extended to student children (up to age 24);
  • Annual Performance Bonus;
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