12 Permanent Biotechnology & pharmaceutical jobs found in Mazowieckie

We are looking for an experienced Senior Regulatory Affairs Professional to support the implementation of regional regulatory strategies for pharmaceutical products at various stages of their lifecycle. This role involves close collaboration with global and regional teams to effectively execute regulatory submission plans, support product approvals, and ensure compliance with local and regional regulatory requirements.what we offerOpportunity to work in a

Are you ready to take your career to the next level with a global organisation? Do you have experience gained in a similar role? We currently have an offer for the position of International Medical Operations Senior Manager at one of our clients from the healthcare industry.what we offerwork based on an employment contract,hybrid work system: 3 days from the office and 2 days of remote work per week, benefits package: supplemental medical plan, sports card

Join one of the largest pharmaceutical companies worldwide as a Regulatory Affairs Director (CMC) and play a pivotal role in shaping the future of global regulatory strategies for pharmaceutical products. This is an exciting opportunity to lead high-performing teams, drive strategic initiatives, and collaborate with global leaders to ensure compliance, innovation, and excellence throughout the product lifecycle.what we offerhybrid model of work for flexibi

For our Client, one of the largest pharmaceutical companies in the world, we are looking for a Regulatory Affairs Manager who will manage the operational delivery of regulatory documents for product registration and compliance. This person will manage the team and coordinate the plans for packages of documents sent.If you have relevant experience and you are ready for new professional challenges, apply for this role.what we offercompany carbeneficial leave

For our Client, one of the biggest Pharmaceutical Companies worldwide, we are looking for a Regulatory Affairs Senior / Specialist in Submission Publishing who will be responsible for executing the electronic publishing of complex regulatory submissions for national, regional and global regulatory agencies and operating companies in both eCTD and non-eCTD format. If you have relevant experience and would like to participate in the process, apply for this r

For our Client, one of the largest pharmaceutical companies in the world, we are looking for a Regulatory Affairs Specialist who will ensure compliance with regulations and interpretations of regulatory agencies.The Regulatory Affairs Senior Specialist will be responsible for the operational submission management and delivery of regulatory submissions required to support product development, registration and compliance.If you have relevant experience and y

We are seeking a highly skilled Regulatory CMC Manager to play a vital role in shaping global regulatory strategies for innovative pharmaceutical products. In this position, you will lead the preparation of regulatory dossiers, collaborate with cross-functional teams, and provide expert guidance to ensure compliance and successful product development. This is a unique opportunity to contribute to global submission plans, refine regulatory strategies, and d

For our Client, one of the largest Pharmaceutical companies worldwide, we are looking for Regulatory Affairs Mananger / Senior Manager in Global Labeling, who will ensure quality of primary and derived labeling documents and ensure support for the documents.If you have relavant experience and would like to participate in the global labeling strategy, apply for this role.what we offerBeneficial leave policies Medical Care program & Life Insurance Pension pl

Step into a pivotal role as Manager, Regulatory Affairs and contribute to the global development and lifecycle management of groundbreaking pharmaceutical products. As a key member of team, you will lead the development and execution of global CMC regulatory strategies, ensure compliance with regulatory requirements, and represent Global CMC Regulatory Affairs in cross-functional and external collaborations. This is an exciting opportunity to shape global

we are looking for a Senior Manager, Global Labelling to be responsible for the labelling strategy for pharmaceutical products in international markets. The role requires close collaboration with global and regional teams and subject matter experts to ensure documentation is in line with regulatory requirements and business strategy.the incumbent will manage the processes for developing, approving and updating labelling documents, coordinate the Labeling W

Приєднуйтесь до команди Randstad і почніть роботу у найбільшого дистриб'ютора фармацевтичних препаратів!Сучасний, великий і чистий склад без шуму i пилу!Робота проста і фізично не важка. Ви зможете швидко всьому навчиться!Зручний доїзд міським транспортом з Warszawa, Ożarów Mazowiecki, Grodzisk Mazowiecki, Pruszków!Залиште свою заявку прямо зараз і наші фахівці розкажуть вам більш детально про дану вакансію!пропонуємо погодинна ставка 33,00 zł brutto/год,

Присоединяйтесь к команде Randstad и начните работу у крупнейшего  дистрибьютора фармацевтических препаратов!Современный, большой и чистый  склад  без шума и пыли!Работа  простая и физически не тяжелая. Вы сможете быстро всему научится!Удобный доезд городским транспортом с таких локаций как:  Warszawa, Ożarów Mazowiecki, Grodzisk Mazowiecki, Pruszków!Оставьте свою заявку прямо сейчас и наши специалисты расскажут Вам более подробно о данной вакансии! предла