QA Officer

Novartis; Zaragoza; Presencial; EUR 30.000 - 40.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in Zaragoza is seeking a QA Officer to ensure quality oversight in GMP activities. Responsibilities include supervising hygiene, maintaining quality systems, and managing documentation. The ideal candidate holds a scientific degree and has at least one year of experience in a Quality department. Fluent English is required. This role offers a full-time position with a focus on quality assurance.

Formación

• 1 year of experience in a Quality department.
• Strong affinity with and awareness of Quality issues.
• Solid knowledge of quality system (GMP) and basic knowledge of regulatory requirements.

Responsabilidades

• Supervise the hygiene conditions of the premises.
• Ensure validation/qualification status of production site equipment.
• Responsible for the provisional release for the shipment of batches.

Conocimientos

Quality oversight

Organizational skills

Attention to details

Fluency in English

Educación

Scientific degree in Pharmacy, Chemistry, or Biology

Descripción del empleo

Job Description Summary

The QA Officer guarantees the quality oversight over the entire working time of the facility for all the GMP activities on going.

Job Description

Major accountabilities :

• Supervise the general conditions of hygiene of the premises subject to its management
• Contribute in assuring the validation / qualification status of the production site equipment training of personnel and management of quality documentation
• Responsible for the provisional release for the shipment of batches
• Work in shift with other QA officers to oversight the production and quality control activities.
• Archiving and support in managing the site GMP documentation review of batch records and assure the timely closure of the manufactured batches.
• Contribute in maintaining the local quality system as per GMPs and corporate guidelines and in assuring the respect of the GMPs and Health Authorities requirements at local level
• Support the QP in the preparation of batches release documents
• Collaborate in redaction of site GMP documentation and preparation and printing of batch documentation
• Support during the external audits by the authorities and corporate audits
• Collaboration in data compilation of Product Reviews oversight on investigations and monitoring of resulting actions are checked and approved.
• Participate to the self-inspections as per approved annual plan and to the external audits
• Be responsible for the appropriate level of quality oversight during the GMP activities of the facility verifying they are executed according to the applicable standards in manufacturing quality control distribution and quality processes.

Minimum Requirements :

• Education: Scientific degree in Pharmacy Chemistry or Biology
• 1 year of experience in a Quality department.
• Strong affinity with and awareness of Quality issues
• Good organizational skills including attention to details
• Solid knowledge of quality system (GMP) and basic knowledge of regulatory requirements
• Fluent English verbally and in writing

Employment Type

Full-Time

Vacancy

1