We are looking for a QC – Analytical Manager for a newly established pharmaceutical company in Spain: Job Description: As the manager, you will be responsible for creating the QC Analytical department, team, and procedures from scratch. As the Quality Control Manager, you will lead quality control to ensure the integrity and compliance of our products. You will oversee testing, validations, and regulatory activities, managing a dedicated team and collaborating with cross-functional teams to continuously improve quality processes. Key Responsibilities: - Supervise quality control testing of raw materials, intermediates, and finished products. - Develop and implement testing procedures and methods. - Coordinate sampling, testing, and product release. - Lead the validation and qualification of analytical methods. - Collaborate with Quality Assurance to investigate and resolve deviations. QC – ANALYTICAL MANAGER Solo Talento | (10) ofertas activas Empresa que ofrece el puesto: Pharmaceutical company Valencia 11 Jun. - - Descripción We are looking for a QC – Analytical Manager for a newly established pharmaceutical company in Spain: Job Description: As the manager, you will be responsible for creating the QC Analytical department, team, and procedures from scratch. As the Quality Control Manager, you will lead quality control to ensure the integrity and compliance of our products. You will oversee testing, validations, and regulatory activities, managing a dedicated team and collaborating with cross-functional teams to continuously improve quality processes. Key Responsibilities: - Supervise quality control testing of raw materials, intermediates, and finished products. - Develop and implement testing procedures and methods. - Coordinate sampling, testing, and product release. - Lead the validation and qualification of analytical methods. - Collaborate with Quality Assurance to investigate and resolve deviations. Número de vacantes: 1 Modalidad de trabajo: Presencial Tipo de contrato: Indefinido " Requisitos - Bachelor's or Master's degree in Chemistry, Biochemistry, Microbiology, Pharmaceutical Sciences, or related fields. - 8-10 years of experience in quality control within the biopharmaceutical or vaccine industry. - Experience in directly leading teams. - Knowledge of cGMP, FDA, EMA, and ICH regulations. - Experience in method validation and analytical testing. - Fluent in English. - Leadership, communication, and problem-solving skills. en Ciencias Artísticas Estudios mínimos Licenciado Especialidad: Química, Bioquímica, Microbiología, Farmacia Idiomas Inglés nivel Alto. Experiencia mínima de 5 a 10 años Disponibilidad para viajar Ninguna #J-18808-Ljbffr
