Group Quality Specialist (m/f/d) - Specifications

Job-ID: 60985Location: Wien, AUTJob Level: ProfessionalsCategory: QualityEmployment Type: Temporary employmentBecome part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation.With over 1600 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location.Join us in shaping our vision to provide new health solutions advancing human life.Your Main Tasks And ResponsibilitiesDefine requirements and testing criteria for raw materials and other incoming goods, ensuring they are clearly documented in specificationsAssess, initiate, and manage change controls resulting from supplier change notifications or updates to pharmacopoeial requirementsSupport the lifecycle management of raw materials and other incoming goods, including initiating Change Controls for phase-out activitiesPerform administrative and documentation tasks related to specification management and change control processes for raw materials and incoming goodsContribute to continuous improvement initiatives within quality systems and support harmonization projects across functions or sitesYour expertise and ideal skill setEducational background and/or University degree in Chemistry, Biochemistry or a related field Professional experience in pharmaceutical industry especially in the field of quality control (GMP environment) is a plusSkilled in using MS Office and SAPProfessional use of English and German language, both written and oralStrong interpersonal communication and organizational skills Your department - where you make an impactWe, the Group Quality department, are responsible for developing policies and procedures for all CQ Plasma activities based on current applicable regulations, ensuring a standardized approach throughout the organization.Our team is divided into CQ Plasma, CQ Control, Corporate Stability Studies, Corporate QC Method Validation, and Corporate QC Incoming Goods.Thrive with usCompany restaurant & meal subsidy Training & further education Health promotion Parking spaces and good public transport connections Company and team events Enjoy these attractive benefits! You can find all offers here: BenefitsThe minimum gross salary according to the collective agreement (chemical industry) is EUR 4,270.14 based on 38 hours per week (full-time). As we strive to offer a salary that reflects your individual profile and qualifications, there is a willingness to pay above the minimum salary.It´s in our bloodWe live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.Do you have any questions? Then get in touch with your contact person.Mrs. Johanna ProkschOctapharma Pharmazeutika Produktionsges.m.b.H.Oberlaaer Straße 235, 1100 WienT: +43 (1) 610 32 - 4299You can also reach us Monday to Friday via WhatsApp: +43 (0) 664 88578113Want to find out more about us?Visit our website Octapharma Career and follow us daily on LinkedIn.About OctapharmaOctapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide.Apply now