Aurora Deutschland GmbH, headquartered in Berlin, is one of the largest licensed manufacturers and distributors of medical cannabis under MedCanG. The company is also a GMP-certified importer of medicinal products. The medical cannabis products it distributes are medicinal products in accordance with AMG § 2 (1) and raw materials in accordance with § 11 of the ApBetrO. The company is part of Aurora Europe GmbH, which in turn is a subsidiary of the publicly traded Canadian cannabis producer Aurora Cannabis Inc., headquartered in Edmonton, Alberta. In addition to its import and wholesale license, Aurora Deutschland also has a manufacturing license. Further information can be found at www.auroramedicine.com. At our Berlin location (near the Innsbrucker Platz S-Bahn and U-Bahn station), we are looking for you as Manufacturing Assistant (m/f/d) (Documentation) to join our team as soon as possible. As a Manufacturing Assistant, you play a key role in ensuring the smooth execution of our manufacturing processes with external contract manufacturers. You will prepare manufacturing orders, review batch documentation, approve batch-specific labels, and ensure that all records meet GMP standards. In your function as Deputy Head of Production (LdH), you support operational continuity and GMP compliance in the absence of the Head of Production, working closely with teams such as Quality Assurance and Supply Chain Management. Your Responsibilities Act as Deputy Head of Production (LdH) in accordance with §12 AMWHV and EU GMP requirements Prepare and issue manufacturing orders Review and approve batch-specific labels Check batch records for completeness and accuracy Confirm GMP compliance of manufacturing activities and documentation Review invoices within your area of responsibility Support the creation and maintenance of SOPs in line with GMP standards Participate in change control activities related to manufacturing Support the preparation and execution of self-inspections together with Quality Assurance Collaborate with Quality Assurance and SCM to ensure seamless processes and regulatory compliance Support SCM with planning, production, and logistics topics Handle sensitive data and manufacturing records with the highest level of confidentiality and accuracy Perform other tasks as assigned by the department management Qualifications Degree in natural sciences (e.g., Biology, Biochemistry) or equivalent qualification (BTA/PTA) Confident use of MS Office and digital documentation tools Strong knowledge of regulatory frameworks (AMG, AMWHV, GMP) Experience in a GMP‑regulated environment is an advantage High attention to detail and strong quality mindset Fluent German and good English skills (written and spoken) Reliable, structured, and proactive working style Ability to prioritize and manage multiple tasks Good communication and collaboration skills We offer You A career at the European leader in medical cannabis, one of the youngest and fastest growing sectors globally Full-time employment Family-friendly working hours (Monday-Friday) 30 vacation days (per calendar year) Hybrid working arrangement (mix of presence and remote work), with regular presence required on site Daily coffee, fruit and snacks in the office To keep our employees happy and fit, we offer a sponsored membership to the Urban Sports Club Have we caught your attention? We look forward to receiving your online application, including your CV, salary expectations, cover letter and your desired starting date. Please note that applications missing these information will not be considered. You find our data protection declaration for the recruiting process here: https://www.auroramedicine.com/de/datenschutz-bewerber