Qualifications: Bachelor's degree in chemical engineering or similar field
Responsibilities:
Coordinate and manage qualification and validation programs.
Supervise the implementation of new lines and changes in legislation and regulation (FDA and corporate).
Act as a liaison with other managers in areas of quality, development, critical systems and human resources.
Ensure compliance with FDA, NOM-059, ICH, and European manufacturing practices and regulations.
Required Skills:
5 years of experience in medical industry
Experience in handling audits and systems regulated by the FDA for exports to the USA
Experience with FDA regulations (NOM-059, ISH, European and US manufacturing practices).
Knowledge in GMP´s, GLP, PDA, ICH, FDA
Advanced English language skills (at least B2 Level)
Our offer to you:
Life Insurance
Dental insurance
Food vouchers
Major medical insurance
Floating days
Savings fund
Recuerda que ningún reclutador puede pedirte dinero a cambio de una entrevista o un puesto. Asimismo, evita realizar pagos o compartir información financiera con las empresas.