BIOCHEMICAL QC SUPERVISOR

JR Italy; Siena; In loco; EUR 40.000 - 80.000; Tempo pieno

Descrizione del lavoro

An established industry player in the biotech sector is on the lookout for a Biochemical Quality Control Supervisor. This role involves managing laboratory functions, ensuring compliance with quality standards, and driving continuous improvement within the QC team. The ideal candidate will possess a strong scientific background and extensive knowledge of GMP, along with expertise in chromatographic techniques and method validation. Join a dynamic working environment where your contributions will help shape innovative anti-tumor therapies and enhance quality control operations.

Servizi

Dynamic Working Environment

Permanent Contract

Competenze

• Strong scientific background and comprehensive knowledge of GMP.
• Experience with chromatographic techniques and method validation.

Mansioni

• Manage biochemical laboratory functions and documentation.
• Oversee quality control of materials and products.

Conoscenze

Scientific Background

Knowledge of GMP

Chromatographic Techniques

Chemical-Physical Analytical Determinations

Method Validation and Transfer

Proficiency in English

Descrizione del lavoro

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Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is seeking a highly motivated and qualified Biochemical Quality Control Supervisor, who will report directly to the Quality Control Manager.

Responsibilities include:

• Managing biochemical laboratory functions and documentation to support product disposition.
• Overseeing quality control of incoming materials, in-process samples, and finished products.
• Setting up, validating, transferring analytical methods, and writing reports.
• Ensuring laboratory procedures comply with Philogen Quality standards and GMP regulations.
• Supporting daily scheduling activities in collaboration with the QC manager.
• Driving continuous improvement in QC operations and systems, and supporting plant goals. Coaching and developing QC team members to achieve high performance.
• Supporting laboratory colleagues to complete tests and investigations timely, maintaining updated knowledge in technical, operational, and regulatory fields.
• Promoting technological innovation and scientific understanding to design an integrated analytical development strategy within the QC team.

Ideal candidate should have:

• A strong scientific background.
• Comprehensive knowledge of GMP.
• Knowledge of chromatographic techniques such as Size Exclusion Chromatography and Cation Exchange by HPLC, as well as common biological tests (e.g., Bioactivity, ELISA).
• Experience with chemical-physical analytical determinations.
• Knowledge of method validation and transfer, compliant with EP/USP standards.
• Proficiency in English.

We offer:

• A dynamic working environment.
• A permanent contract with a salary based on experience.

Job location:

Interested candidates are invited to submit their applications, expressly authorizing the processing of personal data in accordance with Legislative Decree 196/2003. Our recruitment process adheres to Legislative Decree 198/2006, and we welcome applications from candidates of any gender, orientation, age, ethnicity, or religious belief.