Supplier Quality Officer Geleen • Basic Pharma

Basic Pharma is a unique Dutch pharmaceutical company that is growing at lightning speed, is constantly building its organization and is constantly specializing and developing. The company focuses on the full breadth of the pharmaceutical industry: from product development, registration, production and commercialization of (bio) pharmaceutical products to pharmaceutical services,

Basic Pharma has an ever-increasing circle of national and international customers, from start-ups to multinationals.
The production organization Basic Pharma Manufacturing makes products such as nasal sprays, filled syringes, creams and ointments. In addition, it also supplies clinical study medications and offers various services to third parties, such as quality control and contract manufacturing.

The availability and combination of all activities under one roof makes Basic Pharma a strong and versatile player within the pharmaceutical industry. Currently there are approximately 250 employees. Basic Pharma's ambitions go further and that is why we are looking for employees who are committed, who consider professionalism of paramount importance and who put the customer first. Does this appeal to you? Then the vacancy below might be something for you!

                                                                                                We are looking for a 

                                                                                               Supplier Quality Officer

As our Supplier Quality Officer, you’ll play a vital role in managing and optimizing the supplier quality process across the entire supply chain. You will serve as the key point of contact between QA and our suppliers, ensuring alignment with GMP, ISO13485, MDR, and related regulations. Your work will directly support product safety, regulatory compliance, and our continuous improvement initiatives.

• Qualify suppliers, based on audit reports and questionnaires;
• Investigate material non-conformities and collaborate on resolutions;
• Monitor and manage supplier deviations and complaints in our eQMS;
• Lead and support CAPAs, risk assessments, and quality improvements;
• Review and manage Supplier Quality Agreements;
• Define and track supplier performance indicators (KPIs) and perform annual supplier assessments;
• Actively participate in cross-functional teams to drive compliance and quality;
• Act as subject matter expert for supplier quality during audits.

• You have at least 1 year of experience in quality management within a GMP and/or ISO13485 environment;
• You hold an HBO degree, ideally in a technical or biomedical field;
• You’re analytical, proactive, and confident in managing complex stakeholder interactions;
• You can balance regulatory detail with a pragmatic, solution-focused mindset;
• You communicate clearly and persuasively in English.

• Be part of a mission-driven organization improving patient outcomes;
• Work alongside experienced professionals in a collaborative and quality-focused environment;
• Influence key supply chain processes and drive real change;
• Competitive salary, strong benefits, and a commitment to your professional growth.

Acquisition in response to this vacancy is not appreciated.