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€30,200.00 - €56,000.00
Job Description Summary
LI-Onsite
Location: La Almunia de Doña Godina, Spain
This role is La Almunia de Doña Godina, Spain. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Job Description
Major Accountabilities
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- 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
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- 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
- 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
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- Education: Scientific degree in Pharmacy, Chemistry or Biology
- 1+ years of experience in a Quality departmen