Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
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
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
Collaboration in data compilation of Product Reviews, oversight on investigations and monitoring of resulting actions are checked and approved.




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.
1+ years 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
~ Fluent English verbally and in writing

global recognition programs
flexible and hybrid working options, where possible
In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Read our brochure to learn more about our general total rewards offering:
Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. Skills Desired Collaboration, Data Integrity, Leadership, Operational Excellence

📌 Quality Manager QA/qc (Zaragoza)
🏢 Healthcare Businesswomen’s Association
📍 Zaragoza