Quality Assurance Coordinator - Pharma (On-Site)

Hikma Pharmaceuticals; Sintra; Presencial; EUR 30 000 - 45 000; Tempo integral

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

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