QA Officer

FCRS = IT058; Ivrea; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company in Ivrea, Italy is seeking a QA Officer to ensure quality oversight for ongoing GMP activities. The ideal candidate will have a scientific degree and prior experience in a sterile environment, with the ability to work shifts. Proficiency in Italian and good English knowledge are essential. This full-time role involves reviewing documentation and supporting batch releases, ensuring compliance with GMP guidelines.

Competenze

• Previous experience in a similar role within a sterile pharmaceutical or biotech environment.
• Available to work in shifts including night shifts and weekends regularly.
• Fluent in Italian and good knowledge of English.

Mansioni

• Guarantee quality oversight for ongoing GMP activities.
• Contribute to maintaining local quality system as per GMPs.
• Review batch records and assure timely closure of batches.
• Support QP in preparing batches release documents.

Conoscenze

Continued Learning

Dealing With Ambiguity

Gmp Procedures

Qa (Quality Assurance)

Quality Control (Qc)

Testing

Quality Standards

Self-Awareness

Technological Expertise

Technological Intelligence

Formazione

Scientific degree

Descrizione del lavoro

Job Description Summary

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

Major Accountabilities

• Contribute to 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 to 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.
• Involvement in investigation of deviation OOS complaints CAPA change control implementation and redaction.
• Collaborate and support during the external audits by the authorities and corporate audits.
• Contribute to redaction and review of SOPs records protocols and reports according to GMPs National / Corporate Guidelines and health authorities requirements.

Essential requirements

Scientific degree.

Previous experience in a similar role within a sterile pharmaceutical or biotech environment.

Available to work in shifts including night shifts and weekends (on a regular basis)

Fluent in Italian. Good knowledge of English.

Skills Desired

• Continued Learning
• Dealing With Ambiguity
• Gmp Procedures
• Qa (Quality Assurance)
• Quality Control (Qc)
• Testing
• Quality Standards
• Self-Awareness
• Technological Expertise
• Technological Intelligence

Required Experience

Unclear Seniority

Key Skills

Graphic Designing,Information Technology Sales,IT Services,Accounts,Auto Parts,Import & Export

Employment Type

Full-Time

Experience

years

Vacancy

1