Quality Assurance Specialist

JR Italy; Reggio Emilia; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading HR services provider is seeking a Quality Assurance Specialist in Reggio Emilia. The role involves monitoring quality control, investigating complaints, and supporting audits in a biomedical company. A Master's degree in relevant fields is required, along with strong communication skills and experience in quality assurance.

Competenze

• 1-3 years experience in quality assurance.
• Knowledge of ISO 13485 and Medical Device Directive.

Mansioni

• Monitor quality control of chemical products.
• Investigate product complaints and implement corrective actions.
• Support periodic review of internal control procedures.

Conoscenze

Interpersonal Skills

Communication Skills

Collaboration

Formazione

Master's degree in Chemistry

Pharmacy

Pharmaceutical Technology

Strumenti

Office Equipment

Software Proficiency

Descrizione del lavoro

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Quality Assurance Specialist, reggio emilia

Client: Gi Group

Location: Reggio Emilia, Italy

Job Category: Other

EU work permit required: Yes

Job Reference: 47977728037407948833711

Job Views: 2

Posted: 12.05.2025

Expiry Date: 26.06.2025

Job Description:

Gi Group, Italy's leading employment agency with over 200 branches nationwide and more than 1800 HR professionals, is seeking a Quality Control Specialist for a biomedical company in Parma province.

Responsibilities include:

• Monitoring quality control of chemical products
• Investigating product complaints and implementing corrective actions
• Identifying improvement opportunities in the QA department
• Supporting periodic review of internal control procedures
• Collecting and analyzing quality data for reviews and management assessments
• Assisting in internal and external audits
• Developing corrective action plans based on audit findings
• Maintaining personnel training records in collaboration with HR

Requirements:

• Master's degree in Chemistry, Pharmacy, or Pharmaceutical Technology (CTF)
• Knowledge of ISO 13485, Medical Device Directive 93/42/EEC, and related standards
• Experience with disposable medical devices and auditing activities
• Proficiency with office equipment and software

Characteristics:

• Strong interpersonal and professional communication skills
• Experience of 1-3 years in the field
• Ability to work collaboratively in an office environment
• Flexibility and resilience in facing challenges
• Effective interaction with team members and external collaborators

Offer: Fixed-term contract with potential for permanent employment; competitive salary based on experience; location in Parma province, Fiorenzuola (PC).

Gi Group Holding is a leading multinational HR services provider operating in over 37 countries, committed to values like collaboration, innovation, and responsibility. Visit www.gigroupholding.it for more info.

Gi Group S.p.A. is authorized by the Italian Ministry of Labour and Social Policies. We promote equal opportunity employment in compliance with applicable laws. Candidates are encouraged to read our privacy policy at www.gigroup.it/privacy-candidati.