Quality Operations Manager

Contenido de trabajo

Make your mark for patients. We’re here because we want to build the future and transform patients’ lives for the better.At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?To strengthen our Quality Operations department, based in our site, in Bulle, Switzerland, we are looking for a talented individual to fill the position of: Quality Operations Manager.As a Quality Operations Manager you will manage the team, including Quality Assurance and Quality Control expertises, specifically regarding the microbiological laboratory, to ensure the quality of clean utilities and environment areas of the site plants, as well as the buffers area of the biological plant.You will have to maintain and develop an organization to ensure and optimize an efficient interface with Production, Technical Services and Supply Chain, as well with Quality units of other UCB sites. As manager, you will have to prepare the future as defined by site strategy.You like to work in an environment where you can:Participate to the definition of strategy in terms of Quality Operations for QC and QA processes.Develop and maintain a quality organization supporting quality leadership and technical expertise on pharmaceutical products.Create an impact in a new structure.You will contribute by:Ensuring the laboratory infrastructure maintenance and the continuous improvement of the organization: capacity, cycle times, speed, quantity, losses, yield optimization, etc.Aligning the quality practices with your pairs to gain in agility to maintain and improve operational performance in line with site objectives.Building and maintaining an efficient organization to assure positive impact on Security, Quality, Time and Cost by supporting the development of individuals’ skills and abilities.Encouraging the decision taking at all level by engaging your responsibility, using experiences as learning tool, and developing the teams’ capacity, responsibility and competency.Establishing the investments and functions budget as well as their justifications within the deadlines set out and ensure their follow-up : identify the derives and the required actions.Interested? For this position you’ll need the following education, experience and skills:Master’s degree inConfirmed experience in a GMP regulated environment and technical competence in core areas of medicinal product manufacturing.5+ years professional experience in manufacturing process, laboratory, development, quality control/assurance or regulatory affairs and 2+ years’ experience in people management.Good knowledge of manufacturing process and microbiological techniques.Experience with FDA, European and Japanese investigators during on-site inspections, and experience interacting with Regulatory review staff on submission issues.Excellent interpersonal, verbal, and written communication skills are required, with ability to balance multiple priorities and provide leadership.Stress resistant and capable of risk management behaviour.Fluent in French and English.Why you should applyAt UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.About us.UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science. At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.

Curious to know more? Please visit our website .UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.Job SummaryJob number: 75542Date posted : 2021-06-16Profession: Engineering, Manufacturing, and Supply ChainEmployment type: Permanent