Advanced QA Professional
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Søborg
Would you like to work in one of the most interesting, complex, and dynamic areas in Offering QA support and GMP guidance to our partners and do the final release of packaging from CMOs Ensuring that our products are manufactured according to cGMP and our marketing authorizations Having daily interactions with both internal and external business partners, while expecting a high level of complexity in your tasks The daily QA activities are typically carried out by the contract manufacturers themselves, but the handling of documentation from the contract manufacturers is part of your job. This role will provide you with a wide variety of challenges and opportunities for growth. Since the manufacturers are located outside Denmark, you are expected to travel 5-15 days a year. Qualifications To succeed in this role, you: Hold a MSc in Pharmacy, Engineering or similar At least 2 years of experience from a pharmaceutical organisation where you have gained a solid and up-to-date knowledge of quality and GMP requirements Are a qualified Person (QP) delegate and/or has knowledge of quality assurance of pharmaceutical manufactured products within assembly and pack and/or experience from working as QA for CMO’s Have great cooperation and communication skills with fluency in English On a personal level, you have strong interpersonal skills and a pragmatic approach to problem solving, and are able to organise and drive tasks with your detail-oriented and strong quality mind set. Furthermore, you are a team player who is also able to work independently and can thrive on working across departments in an international organisation. We are looking for an open-minded and straightforward person, with a good sense of humour, outgoing attitude, and natural networking skills. About the department GCM QA is a dynamic department consisting of 40 competent people and is characterised by a high level of professionalism, flexibility and cooperation. Our department is responsible for quality assurance and quality support for outsourced production activities worldwide, as well as setting direction for our Global Contract Manufacturer Organisations worldwide. The open position as Advanced QA Professional, is in the GCM QA Operations FP team, which is responsible for tablets, assembly and packaging at the CMO´s. Working at At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing. Contact For further information, please contact Katrine Hammer on + . Deadline 25th June 2024 You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
which is the Global Contract Manufacturing (GCM) QA? Are you ready to engage, support and mobilise colleagues in an international business environment, where we have both internal and external business partnering with CMO’s? If yes, then this is your opportunity to join our GCM QA team and become our newest Advanced QA Professional! We invite professionals of diverse seniority levels to apply. Take the first step towards an exciting career – apply today! Please note that this position is based at our offices in Søborg. However, we are moving to new offices in Høje Taastrup – expected moving date is in the beginning of 2025. The position As a QA Professional, you will have the opportunity to make a significant impact on the quality assurance of our contract manufacturing for assembly and pack CMOs. Your responsibilities will include:
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Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 28.3.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Søborg
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