Quality Control Analyst

Barrington James; Milano; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A global pharmaceutical company is seeking a skilled Quality Control Specialist based in Milan, Lombardy. This role involves performing analytical method validation and operating lab instrumentation. Ideal candidates have over 3 years of experience and a Master’s degree in a related field. Opportunities for global project participation and career growth are offered. Strong communication skills in Italian and English are mandatory.

Servizi

Competitive compensation

Opportunities for global project participation

Supportive environment and professional growth

Competenze

• 3+ years experience in quality control or related fields.
• Strong understanding of core analytical equipment and routine lab operations.
• Experience integrating analytical data through APIs is required.

Mansioni

• Perform and document analytical method validation.
• Operate and troubleshoot HPLC, GC, and mass spectrometry systems.
• Collaborate with global teams on analytical validation projects.

Conoscenze

Analytical validation

HPLC operations

Mass spectrometry

Chromatographic systems

Teamwork

Bilingual Italian & English

Formazione

Master's degree in scientific discipline

Strumenti

HPLC

GC

Mass spectrometry systems

Descrizione del lavoro

We are seeking a highly skilled Quality Control Specialist with a strong background in analytical validation to support our expanding API Quality department. This role is ideal for a detail-oriented professional who thrives in an international environment and is motivated to grow into leadership and resource-management responsibilities.

Responsibilities

• Perform and document analytical method validation with an emphasis on API testing.
• Operate, maintain, and troubleshoot HPLC, GC, and mass spectrometry systems to ensure reliable and compliant data output.
• Execute routine and advanced analyses using core laboratory instrumentation to support product release and stability programs.
• Collaborate with global teams to contribute to large-scale analytical validation projects.
• Ensure all QC activities meet internal quality standards and regulatory expectations.

What you bring

• 3+ years experience in quality control or related fields - analytical validation using chromatographic and mass‑spectrometric systems is of preference.
• Strong understanding of core analytical equipment and routine lab operations
• Previous experience working with or integrating analytical data through APIs is required
• Eagerness to join a high-performing team involved in international validation projects, with the opportunity to develop into a leadership position.
• Master’s degree in a scientific discipline (chemistry, pharmaceutical sciences, or related field).
• Strong Italian & English communication skills, both spoken and written
• Dependability, clarity in communication, teamwork, and a transparent working style

What We Offer

• Competitive compensation aligned with experience.
• Opportunities to participate in global projects and develop into team-management or resource-oversight roles.
• A supportive environment built on collaboration, precision, and professional growth.

Seniority level

• Associate

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Pharmaceutical Manufacturing

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