QA Analyst: Injectables Quality Assurance & Growth

Hikma Pharmaceuticals; Sintra; Presencial; EUR 28 000 - 36 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Competitive salary

Growth opportunities

Resumo da oferta

Hikma Pharmaceuticals in Portugal is seeking an Analyst, Quality Assurance to join the Quality Assurance Department on-site. Responsibilities include analyzing bulk samples, in-process control during filling, cleaning verification, data entry in daily logs, and verifying production equipment and processes.

The candidate should have a science degree (or equivalent), strong multitasking and attention to detail, English fluency, and solid computer skills, with knowledge of cGMP/FDA regulations.

Qualificações

• Bachelor-like or higher in science; strong analytical mindset.
• Fluent English and good computer skills required.
• Knowledge of cGMP and FDA regulations preferred.

Responsabilidades

• Conducting or verifying analysis of bulk samples.
• Verifying in-process control during batch filling.
• Conducting or verifying cleaning verification for production parts.
• Entering data in daily forms/logs and ensuring accuracy.
• Ensuring equipment and solutions are maintained under validity.
• Sampling finished products for QA testing.
• Performing rounds in production and packaging areas.
• Carrying out inspections in production areas as needed.
• Assisting start-up before/during production.
• Performing aseptic practices and monitoring cleaning/disinfection.
• Approving maintenance requisitions for production releases.
• Training new QA analysts.
• Verifying prints from production equipment.

Conhecimentos

English fluency

Multitasking

Attention to detail

Computer skills

cGMP knowledge

FDA regulations

Formação académica

High School Diploma or Science degree

Ferramentas

LIMS

Microsoft Office

Descrição da oferta de emprego

Hikma Pharmaceuticals in Portugal is seeking an Analyst, Quality Assurance to join the Quality Assurance Department on-site. Responsibilities include analyzing bulk samples, in-process control during filling, cleaning verification, data entry in daily logs, and verifying production equipment and processes.

The candidate should have a science degree (or equivalent), strong multitasking and attention to detail, English fluency, and solid computer skills, with knowledge of cGMP/FDA regulations.