Join Our Mission to Improve Lives Worldwide
Contribute to Stability and Validation activities by performing analytical and documentary tasks in accordance with SOPs, GMP, and regulatory requirements. This opportunity is for a temporary collaboration of 6 months.
The Impact You'll Make
Perform physical and chemical tests within Stability and Validation activities;
Operate and maintain Quality Control equipment and stability infrastructure;
Record and review data, reporting any out-of-specification or atypical results;
Support qualification and computerized system validation activities;
Prepare protocols, test reports, and technical documentation;
Contribute to investigations, CAPAs, and continuous improvement initiatives;
Ensure compliance with GMP, safety standards, and internal Quality procedures;
Collaborate with cross-functional teams as needed.
What You'll Bring:
Degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or Biochemistry or similar;
Good knowledge of analytical and instrumental techniques (eg. HPLC) and wet chemistry;
Knowledge of GMP and ICH stability guidelines;
Good communication and personal interaction skills;
Strong sense of responsibility, integrity and ethics;
Team player;
Strong computer and digital skills.
Create Your
"At Bial there is no such thing as "luck". There is commitment, dedication, and involvement with the Bial project and my team is part of this journey."
Nuno Costa (Senior Manager Qualifications & Projects, Portugal)
Nível de experiência
Júnior
Tipo de emprego
Temporário
Função
Controle de qualidade
Setores
Fabricação de produtos farmoquímicos e farmacêuticos