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Audit Specialist Supplier Quality Department

Alfasigma

Alanno

In loco

EUR 40.000 - 80.000

Tempo pieno

30+ giorni fa

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Descrizione del lavoro

Join a forward-thinking global pharmaceutical company as an Audit Specialist in the Supplier Quality Department. In this vital role, you will lead GMP audits and evaluate supplier performance, ensuring compliance and quality across our supply chain. Your expertise will directly impact patient safety and product excellence. With a focus on continuous improvement, you will work collaboratively with cross-functional teams and support the implementation of robust quality systems. This is an exciting opportunity to make a significant difference in a company dedicated to improving health and quality of life worldwide.

Competenze

  • 2-3 years of experience in pharmaceutical auditing.
  • Solid background in quality system management (QMS).

Mansioni

  • Lead GMP audits and evaluate supplier performance.
  • Support Quality Agreements and maintain Quality Policies.
  • Assist during audits from Regulatory Agencies and Customers.

Conoscenze

Proactive attitude
Teamwork skills
Project management
Continuous improvement mindset
Documentation skills
Regulatory guidance interpretation
Pharmaceutical regulations knowledge
Communication skills in English

Formazione

Degree in science or engineering

Strumenti

Veeva
Trackwise

Descrizione del lavoro

Audit Specialist - Supplier Quality Department

Are you passionate about quality and compliance? Step into a critical role where your expertise ensures the integrity of our global supply chain.

As an Audit Specialist in our Supplier Quality Department, you'll lead GMP audits, evaluate supplier performance, and drive continuous improvement across our sourcing operations. Make a real impact on patient safety and product excellence by joining our team!

Key responsibilities:
  • Perform audits of Third Party Manufacturing, Secondary Packaging, API and Excipient Manufacturing, Analytical Laboratories Suppliers, and medical devices according to an Audit Plan (scheduling, agenda, audit reports, and CAPA monitoring); including sterile and non-sterile products.
  • Travel domestically and internationally to conduct audits.
  • Support and provide input for Quality Agreements with suppliers.
  • Enforce and support the implementation/improvement of existing Quality Systems and processes to ensure compliant operations internally and with external suppliers.
  • Assist in maintaining Quality Corporate Policies and Procedures, and implement new or updated guidelines/regulations within the company.
  • Support Supplier Quality and Local Quality Teams during audits from Regulatory Agencies and Customers.
  • Perform other project duties as assigned to support company products and processes.
Candidate skills:
  • Proactive attitude.
  • Strong teamwork skills across departments.
  • Project management abilities, with effective interaction with internal and external stakeholders.
  • Continuous improvement mindset.
  • Ability to work independently with minimal oversight.
  • Excellent documentation skills and proficiency with office software and electronic Quality Management Systems (e.g., Veeva, Trackwise).
  • Ability to interpret regulatory guidance, company policies, and procedures into executable documentation.
  • Understanding of modern, risk-based validation processes.
  • Deep knowledge of pharmaceutical regulations in major markets (EU, US).
  • Good communication and written skills in English.
Educational and experience requirements:
  • Degree in science or engineering.
  • At least 2-3 years of experience in pharmaceutical auditing, including API & CMO audits (experience with medical devices and food supplements is a plus).
  • Experience in GDP areas.
  • Solid background in quality system management (QMS).
  • Previous experience in quality control laboratories or production areas is advantageous.

About Alfasigma: A global pharmaceutical company founded over 75 years ago in Italy, with operations in over 100 markets worldwide. We focus on research, development, production, and distribution of medicinal products across therapeutic areas such as Gastroenterology, Vascular, and Rheumatology, dedicated to improving health and quality of life.

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