QA Manager / 100% (m/f/d)

Develco Pharma has been active in the production and development of pharmaceuticals with generic active ingredients since 2006. Our experienced team pursues innovative approaches to formulation development, design and clinical trials. The submission of authorisation documents, production and testing, to the packaging of complex medicinal forms, is also part of the daily schedule. Our expertise is delayed or modified releases of active substances to create added value for patients. High-quality formulations - from idea to development, to production Develco Pharma has been active in the production and development of pharmaceuticals with generic active ingredients since 2006. Our experienced team pursues innovative approaches to formulation development, design and clinical trials. The submission of authorisation documents, production and testing, to the packaging of complex medicinal forms, is also part of the daily schedule. Our expertise is delayed or modified releases of active substances to create added value for patients. With digitalization, great people and modern technologies to our vision we produce our quality media in our top modern production site in southern Germany – according to the latest standards. Here, our well-trained employees, with the support of digital technologies, work hard to provide customers and patients with important medicines daily and to increase their quality of life. QA Manager (m/w/d)

Participation and responsibility in one or more competence centers with focus on: Issue Management: Processing of deviations, customer complaints, CAPAs, OOX processes and change control. Audits & Supplier Management: Planning and implementation of internal/external audits, self-inspections and qualification and monitoring of suppliers. QM systems: administration and maintenance of digital QM tools (e.g. SOP-Guard, FORM-Guard), SOP management and design of the corporate process landscape. QM Reporting & Continuous Improvement: Development and maintenance of QA-KPIs, implementation of management reviews and participation in the Product Quality Review. Training: Planning and implementation of training on GMP, QA processes, QA systems and products as well as management of training documents.

Coordination and monitoring of competence center activities incl. Care of dashboards. Interface management for internal and external stakeholders. Developing and developing tools and methods to support the respective topics. Function as an “oscillation damper” in the agile structure according to the Viable System Model (VSM) according to Fredmund Malik – promoting smooth cooperation without direct line function.

Completed scientific or technical studies or equivalent qualification GMP knowledge and experience in quality management, ideally also in pharmaceutical quality control (QC) Experience in one or more areas: Deviation Management, CAPA, Audits, Digital QM Systems, KPI Reporting or Training Analytical thinking, structured and solution-oriented working Very good communication and team skills, high initiative Good knowledge of English and IT affinity

Look forward to a varied and responsible activity in a dedicated, collegial team – with plenty of space for your own ideas and co-design. Your advantages with us: 30 days holiday for your rest Individual training opportunities to promote your development Employee Participation Program – benefit directly from company success Private Accident Insurance & Occupational Pension Insurance JobRad – sustainable and healthy on the move Exclusive employee discounts at well-known brands Regular operating events to strengthen team spirit Free drinks & parking directly at the site