The Werkstudent supports administrative tasks, compiling and processing production data, revising manufacturing documents, and creating guidelines. This role is aimed at assisting in the biopharmaceutical manufacturing process.

Assist in the timely technical review of manufacturing documents for buffer and media preparation, ensure compliance with GMP guidelines, document and track corrections in the IT system Jira, communicate with production and quality assurance teams, and support organizational tasks related to batch documentation.

Rentschler Biopharma is offering high school students the opportunity for a one-week mandatory internship to gain insights and valuable experiences in various vocational fields. Students can explore professions such as logistics, industrial management, dual study programs, chemistry lab technician, and pharmaceutical technician, all guided by trainers and experienced staff.

The External Quality Assurance Associate III serves as the primary Quality contact for customers, reviews and approves documentation for new product introductions, and ensures compliance with regulatory requirements. This role also involves providing training, participating in audits and assessments, and driving continuous improvement initiatives within the Quality department.

Rentschler Biopharma is inviting applicants for a proactive role to contribute to their biopharmaceutical manufacturing team. The role involves engaging within a collaborative work environment focused on producing essential medicines for patients with serious illnesses.

Rentschler Biopharma is seeking candidates interested in a career transition into pharmaceutical production. The role involves working in a collaborative environment to manufacture biopharmaceuticals for patients with serious conditions, and offers opportunities for personal development within a supportive company culture.

As a Process Engineer II, you will engage in project teams working through the full cycle of engineering projects. Responsibilities include supporting equipment selection, implementation, SOP authoring, and validation processes. You will also drive processes to completion, lead capital project initiatives, and collaborate with multi-functional teams to address deviations and regulatory compliance. Your role contributes to the successful integration of manufacturing processes and ensures operational excellence in a biopharmaceutical environment.

The Sr SAP Business Analyst will maintain and develop SAP PS across the corporate group, optimize project management processes, customize SAP PS, integrate it with other SAP modules, provide daily user support and training, and manage global SAP projects while ensuring adherence to time, budget, and quality constraints.

The Director of Quality Assurance Operations leads and develops the Quality Operations team, ensures compliance with regulations, manages daily quality activities, conducts audits, and seeks improvements in processes to enhance quality and efficiency in biopharmaceutical manufacturing.

The Buyer/Planner will manage material procurement and inventory for the biopharmaceutical production, ensuring timely orders and supplier relationships. The role includes strategic sourcing, spend management, and stakeholder interaction to align inventory with production needs while maintaining high-quality standards.

The Process Manager in Upstream MSAT will independently plan and execute complex tasks in customer projects, provide technical support to business development, ensure compliance with regulatory standards, manage customer communications, and oversee the transfer of processes to production sites while leading and developing staff.

The Scientist in Upstream Process Development will develop scalable upstream processes for biopharmaceuticals, utilizing QbD principles and statistical techniques. Responsibilities include process optimization, technology transfer, and technical documentation, while collaborating with cross-functional teams and providing process support on the manufacturing floor.