Pharma Development Scientist - GMP, Tech Transfer & Growth

Galenicum; Comunidad de Madrid; Presencial; EUR 40 000 - 60 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health insurance coverage

Subsidized meals

Gym discounts

Buddy program

Training opportunities

Resumo da oferta

Galenicum is a growing pharmaceutical company seeking a Pharmaceutical Development Scientist in Madrid. You’ll lead development activities, coordinate with partners, and ensure GMP-compliant pilot batches meet deadlines for launches.

Ideal candidates have 2–3 years in pharma development, with English and Spanish proficiency and familiarity with EMEA, FDA, ISO guidelines, plus MS Office skills.

Qualificações

• 2–3 years of experience in pharmaceutical development, production or related dept.
• Experience reading scientific documentation.
• Knowledge of international guidelines EMEA, FDA, ICH and ISO.
• Experience MS Office.

Responsabilidades

• Conduct pharmaceutical development activities, pre-formulation, and pilot batches under GMP.
• Coordinate with clients, suppliers and partners for new drug product development.
• Collaborate with manufacturing and industrial development for scale-up transfer.
• Prepare and review development protocols, reports and manufacturing docs.
• Support regulatory strategy and dossier-related activities.
• Handle QA/TQA and respond to deficiency letters and audits.
• Communicate with stakeholders across the company.
• Travel may be required for manufacturing and transfer activities.

Conhecimentos

Pharmaceutical development

Reading scientific documentation

MS Office

English and Spanish

Formação académica

Degree in life sciences

Master’s degree in Galenical Development and/or Pharmaceutical Industry

Descrição da oferta de emprego

Galenicum is a growing pharmaceutical company seeking a Pharmaceutical Development Scientist in Madrid. You’ll lead development activities, coordinate with partners, and ensure GMP-compliant pilot batches meet deadlines for launches.

Ideal candidates have 2–3 years in pharma development, with English and Spanish proficiency and familiarity with EMEA, FDA, ISO guidelines, plus MS Office skills.