QUALITY ASSURANCE SPECIALIST - GMP (M/F/D)
Descrição da oferta de emprego
Your new role This professional will be responsible for the strategic development of an effective global risk-based, and for lead of GMP/ISO audits according to the requirements specified in the respective company procedures as well as applicable regulations and standards including applicable ISO norms.
This professional also provide technical guidance, mentoring, and training on audit, supplier qualification and supplier quality management activities.
What you'll need to succeed We are looking for professionals with experience in Pharmaceutical or Medical Device Industry, and at least 4 years auditing experience.
Knowledge of international authority regulations (FDA, PICs, ICH), including applicable ISO norms.
Strong interpersonal skills, including diplomacy, communication, negotiation and persuasion, speak and write fluent English are required.
There will be a requirement for international travel of 40% of the time.
What you'll get in return This is an excellent opportunity to join a multinational pharmaceutical company where the human resources are valued.
What you need to know If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
#LI-DNI # - Joana Ganhao
Detalhes da oferta
- Hays
- Em todo Portugal
- Indeterminado - Indeterminado
- Indeterminado
- 16/05/2024
- 14/08/2024
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