Join a leading player in the pharmaceutical and biotech industries, specializing in the development and manufacturing of cutting-edge sterile injectable products. With over six decades of excellence, we pride ourselves on delivering life-changing medicines worldwide.
About Us
At our organization, quality and innovation are at the heart of everything we do. We collaborate closely with pharmaceutical partners to ensure our products meet the highest regulatory standards and exceed customer expectations. Our diverse portfolio includes biologics, small molecules, vaccines, and more, all aimed at improving patient outcomes globally.
Your Role
As a Senior Auditor, Supplier Quality, you'll play a crucial role in our Quality Auditing Team, reporting to the Senior Manager, Quality Supplier. Your focus will be on ensuring our suppliers meet rigorous quality standards across various critical components and services.
Key Responsibilities
Conduct thorough supplier qualification processes, including on-site audits of API vendors, raw materials suppliers, and service providers supporting pharmaceutical manufacturing.
Drive timely execution of Supplier Quality requirements, from audits to risk assessment and mitigation, ensuring compliance and effective corrective actions.
Plan and implement audit assessment strategies, reporting on findings and recommending corrective measures to enhance processes.
Evaluate supplier responses to audit findings, emphasizing root cause analysis and effectiveness of corrective actions.
Manage new supplier requests and lead periodic reviews to uphold compliance and quality standards.
Collaborate closely with Purchasing and Quality Control teams to ensure seamless integration of supplier requirements.
What You Bring
A Bachelor's degree in Science or Engineering is essential.
Minimum of five years' experience in Quality, Manufacturing, or Engineering, with a strong preference for Supplier Quality functions.
Background in pharmaceutical, medical devices, or biologics industries preferred.
Proven expertise in auditing manufacturing facilities, labs, and computerized systems.
Proficiency in root cause analysis, corrective and preventive actions, and quality metrics reporting.
Familiarity with regulatory standards such as FDA cGMP, ISO 13485, and Eudralex is advantageous.
Excellent communication skills and the ability to collaborate effectively across teams.
Willingness to travel up to 75%, including internationally, with flexibility for remote work.
Why Join Us
At our organization, you'll be part of a dynamic team dedicated to transforming healthcare through innovation and excellence. We offer opportunities for professional growth, competitive benefits, and the chance to make a meaningful impact in a global industry.
Apply Today
Discover how your skills can contribute to our mission of delivering high-quality pharmaceutical products worldwide. Join us in shaping the future of healthcare!
Employment Type: Full-Time
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Quality Assurance
Industries
Human Resources Services
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