Pharmaceutical Development Analyst — Growth & Benefits

Hikma Pharmaceuticals; Sintra; Presencial; EUR 32 000 - 46 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Direct contract with Hikma

Competitive salary aligned with the Ro

Life insurance

Health Insurance extended to student/0

Resumo da oferta

Hikma Pharmaceuticals is seeking an Analyst, Pharmaceutical Development (m/f) to join the Pharmaceutical Development team on-site in Portugal. The role involves staying current with regulatory and quality standards, performing analytical method validation and transfers, and supporting documentation and audits.

You will collaborate across teams to ensure compliant development and filing for new products. The ideal candidate has a degree in chemical engineering or chemistry, strong analytical lab

Qualificações

• Bachelor’s degree in chemical engineering, chemistry or similar.
• Demonstrated knowledge of working in an analytical lab environment, of the cGMPs, and ability to follow SOPs and policies.
• Demonstrated ability to operate and troubleshoot analytical techniques and equipment/software.
• Capability of working with others and as part of a team; good problem-solving skills.

Responsabilidades

• Stays updated with regulatory and quality standards, GXP compliance and best practices worldwide.
• Performs method validation, verification, transfer and stability analysis and generates reports and CoAs.
• Manages process validation batches and stability samples for filings across geographies and presentations.
• Supports management of critical documents and CAPA; preparation of quality management and audit reviews.
• Acts as primary contact for sites to support the introduction of assigned products.

Conhecimentos

Analytical lab experience

cGMPs knowledge

SOP adherence

Teamwork

Formação académica

Bachelor’s degree in chemical engineering or chemistry

Ferramentas

Laboratory equipment operation

Descrição da oferta de emprego

Hikma Pharmaceuticals is seeking an Analyst, Pharmaceutical Development (m/f) to join the Pharmaceutical Development team on-site in Portugal. The role involves staying current with regulatory and quality standards, performing analytical method validation and transfers, and supporting documentation and audits.

You will collaborate across teams to ensure compliant development and filing for new products. The ideal candidate has a degree in chemical engineering or chemistry, strong analytical lab