Regulatory Affairs Associate
Hays AB / Biomedicinjobb / Södertälje
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hela Sverige Regulatory Affairs Associate - AstraZeneca - Södertälje - 12-month consultancy assignment
Are you passionate about the application of science to deliver life-changing medicines?
We are looking for a Chemistry, Manufacturing and Controls (CMC) Regulatory Affairs Associate to join us at Södertälje on a 12-month contract.
Our Chemistry, Manufacturing, and Controls (CMC) Regulatory function spans across the product lifecycle and are responsible for the regulatory strategy relating to the development, manufacture and testing of all of our medicines.
With our expertise, we interpret, anticipate and shape global Health Authority expectations to build insightful CMC and Device Regulatory Strategies. We are the bridge between our R&D functions, Operations sites, Quality and Global Supply Teams in helping safe, effective medicines reach the right patients at the right times. We manage the timely preparation and delivery of CMC contributions to the regulatory submissions linked to medicinal products throughout the commercial lifecycle through to divestment.
What you'll do:
Being a CMC RA Associate within the CMC RA Business Development Team means you are responsible for providing support to Chemistry, Manufacturing and Control (CMC) regulatory contributions required for the management of Product Divestments to 3rd Party Customers. Part of a dynamic team that works closely with both relevant AZ stakeholders and Customers providing regulatory and compliance advice/information as appropriate to ensure compliant supply of product to Customers. The role holder will ensure, where appropriate, the application of global CMC regulations and guidance within AstraZeneca to support Customer interactions and contribute to updates of processes as appropriate.
Responsibilities:
• As necessary, assist in the preparation of regulatory submissions, compilation of submission documentation, and preparation of regulatory components in line with Customer requirements/timelines and management of information.
• Responsible for uploading, retrieval, and maintenance of documents for electronic submissions using the appropriate software and applications.
• As necessary, ensure maintenance and filing of regulatory-related documentation and track regulatory commitments, submission requests, and deliverables to facilitate efficient transfer of registered information to the 3rd Party Customer.
• The role holder will train, guide and advise others, develop training and user support materials, e.g. job aids, work instructions, training videos, e-learning.
• Business administration of systems, e.g. provision of system access, application of security models and managing change.
• Interact with cross-functional groups and attend team meetings as necessary to support submission development and project coordination.
• Assist in the preparation of agendas, presentations, and other supporting materials for various meetings.
• Contribute to the development and improvement of related business processes.
• Ensure the learning from your own projects is shared with other colleagues/within the functions.
Essential for the role:
• Foundational / Associate degree in Regulatory Sciences, Pharmacy, or Pharmaceutical Sciences
• Team working skills
• IT Skills
• Experience in Regulatory Affairs or Quality Assurance.
Desirable for the role:
• Bachelors degree in Science, Regulatory Sciences, Pharmacy, Pharmaceutical Sciences
• Basic knowledge of the regulatory submission process.
• Understanding of current regulatory CMC requirements.
• Basic Understanding of regulations and guidance governing the manufacture of biotechnology products.
• Professional Capabilities - Lean Approach
• Quality Risk Management
Join us to drive strategic success and make a significant impact in the healthcare landscape.
I&D
We are proud to have a unique workplace culture that inspires innovation and collaboration! Here, employees are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.
Why AstraZeneca?
At AstraZeneca, we are on a journey to bring life-saving medicines to patients. Our role in contributing to decreasing mortality rates globally is clear. We shape the future by spotting scientifically-led commercial opportunities and acting now to operationalise and scale them. Driven by the solutions we bring to the healthcare ecosystem, we make an impact at every step of the patient journey. Our specialised team of trusted BioPharmaceuticals experts nurtures innovation and experimentation. We thrive on energy and pace, constantly thinking big to answer new challenges. Join us in improving patient experiences and health outcomes.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.
Ersättning Not Specified
Så ansöker du Sista dag att ansöka är 2025-04-11
E-post:
Hays.80475.3101@haysse.aplitrak.com Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "900942".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Hays AB (org.nr 556640-6103)
Arbetsplats Hays
Kontakt Linnea Killander
linnea.killander1@hays.com +46 8 588 043 00 Jobbnummer 9257907
Observera att sista ansökningsdag har passerat.