Pharmaceutical Development Analyst — Growth Opportunities

Hikma Pharmaceuticals; Sintra; On-site; EUR 32,000 - 42,000; Full time

Benefits offered by this job

Life insurance

Health Insurance

Job summary

Hikma Pharmaceuticals Portugal seeks an Analyst, Pharmaceutical Development (m/f) to join the on-site Pharmaceutical Development team. You will stay up to date with regulatory and quality standards, perform method validation and stability studies, and support CoAs and documentation.

The role requires a bachelor’s degree in chemical engineering or chemistry, lab experience, and knowledge of cGMP and SOPs. Hikma offers a direct contract, competitive salary, life/health insurance, and growth

Qualifications

• Bachelor’s degree in chemical engineering, chemistry or similar.
• Knowledge of regulatory and quality standards (GXP) and ability to follow SOPs.
• Experience in analytical lab environments and ability to operate lab equipment and software.

Responsibilities

• Stay updated with regulatory and quality standards (GXP) globally.
• Perform method validation, verification, transfer and stability samples and generate reports/CoAs.
• Manage process validation batches and stability samples for filings; support document management and audits.
• Act as primary contact for sites to support product introductions.

Skills

Analytical skills

Teamwork

Problem solving

cGMP knowledge

Education

Bachelor’s degree in chemical engineering or chemistry

Tools

Analytical instruments

Laboratory software

Job description

Hikma Pharmaceuticals Portugal seeks an Analyst, Pharmaceutical Development (m/f) to join the on-site Pharmaceutical Development team. You will stay up to date with regulatory and quality standards, perform method validation and stability studies, and support CoAs and documentation.

The role requires a bachelor’s degree in chemical engineering or chemistry, lab experience, and knowledge of cGMP and SOPs. Hikma offers a direct contract, competitive salary, life/health insurance, and growth