GMP QA & Compliance Specialist

BSP Pharmaceuticals S.p.A.; Latina; Presencial; EUR 35.000 - 40.000; Jornada completa

Descripción de la vacante

BSP Pharmaceuticals S.p.A invites a skilled QA professional to join our CDMO operations in Italy. You will review batch records, support investigations, and help keep GMP documentation up to date across QA and manufacturing areas.

The role emphasizes compliance, change control, and safety, requiring a strong attention to detail and the ability to draft clear reports in English. Competitive salary and career growth offered in a multinational setting.

Formación

• MA degree in Chemistry or related field.
• English working knowledge.
• Great can-do attitude.

Responsabilidades

• Batch Record Review: ensure compliance and completeness of batch records and SOPs.
• Investigation Management: assist in deviations and complaints investigations and CAPA reports.
• Procedures: keep SOPs up to date and draft required documentation per GMP.
• Change Management: assist in change assessments and reports.
• Safety: adhere to EHS obligations per applicable regulations.

Conocimientos

English proficiency

Can-do attitude

Educación

MA degree in Chemistry or related field

Descripción del empleo

BSP Pharmaceuticals S.p.A invites a skilled QA professional to join our CDMO operations in Italy. You will review batch records, support investigations, and help keep GMP documentation up to date across QA and manufacturing areas.

The role emphasizes compliance, change control, and safety, requiring a strong attention to detail and the ability to draft clear reports in English. Competitive salary and career growth offered in a multinational setting.