Associate GMP Compliance Auditor (m/w/d) Pharma in Ludwigshafen am Rhein (1665)

Your entry into the pharmaceutical industry – shape quality in the GMP area actively with.

Together with BRÜGGEN ENGINEERING, you will support the quality assurance of leading pharmaceutical and healthcare companies. As an Associate GMP Compliance Auditor (m/w/d), you will take on early responsibility in global quality management, participate in audit processes, and develop yourself step by step into a competent auditor in a regulated environment. An ideal position for committed professionals who want to start or further build their career in pharma and quality assurance.

Aufgaben

• Auditunterstützung: Taking over defined tasks in the audit execution, planning, and scheduling at external service providers – under the guidance of management.
• Lieferantenmanagement: Participating in supplier evaluations, i.e., supporting the maintenance of the supplier list and the global audit plan.
• Audit-Support: Supporting external partners and internal cooperation with Inspection Management within the framework of official or customer audits.
• Datenanalyse: Collecting and preparing internal and external audit key figures as a basis for quality and trend analyses.
• Systempflege: Participating in the further development and updating of QA systems, processes, and documents.
• Regulatorische Anforderungen: Identifying and escalating quality-relevant questions to ensure regulatory requirements.

Qualifikation

• Qualifikation: Completed studies in Life Sciences, Engineering, Quality Management, or a comparable field, or relevant combination of education and work experience will also be considered.
• Erfahrung: First professional experience in the pharmaceutical industry in quality assurance or quality management, practical laboratory or production experience desired.
• GMP-Erfahrung: Initial knowledge of cGMP requirements and interest in quality management, audit processes, or regulatory affairs.
• Motivation: Strong interest in pharma, healthcare, and working in regulated environments.

Benefits

• Attraktive Konditionen: Look forward to an unlimited full-time position at BRÜGGEN ENGINEERING in Mannheim, with a remuneration that values your expertise.
• Innovationsführerschaft: Take on responsibility in the pharmaceutical industry and coordinate projects that efficiently and future-oriented shape the organization of clinical trial matrices.
• Dynamisches Team: Become part of a team that places value on personal growth and a culture of support and promotion.

We look forward to your comprehensive application documents with
specification of your earliest start date and salary expectations.

Your contact person for your application is:
Mr. Dipl.-W.-Ing. Thorsten Schermann

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