CMC Regulatory Affairs Associate

Publiceringsdatum: 2024-10-10

Letar du efter anställning inom yrken med teknisk inriktning? Positionen som kvalitetsingenjör, kemiteknik/kvalitetstekniker, kemiteknik hos Hays AB är öppen och väntar på en lämplig kandidat - kan det vara du? Hays AB söker någon som vill arbeta heltid under 6 månader eller längre. Kanske är det du?

Arbetsplatsen ligger nära tillhands om du är bosatta i Södertälje som är tjänsteorten. Om du letar efter en spännande karriär inom kvalitetsingenjör, kemiteknik/kvalitetstekniker, kemiteknik-branschen, har Hays AB just nu två lediga jobb som kan vara av intresse. Hays AB letar efter erfaren kvalitetsingenjör, kemiteknik/kvalitetstekniker, kemiteknik som kan ansluta till deras team. Sista ansökningsdag är söndag den tjugonde oktober 2024.

Jobbannons

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 our client, AstraZeneca, in Södertälje (SE) on a 12-month contract.

Chemistry, Manufacturing, and Controls (CMC)

Our client's Chemistry, Manufacturing, and Controls (CMC) Regulatory function spans across the product lifecycle and is responsible for the regulatory strategy relating to the development, manufacture, and testing of all their medicines. With their expertise, they interpret, anticipate, and shape global Health Authority expectations to build insightful CMC and Device Regulatory Strategies. They are the bridge between their R&D functions, Operations sites, Quality, and Global Supply Teams in helping safe, effective medicines reach the right patient at the right times. They 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. You will be part of a dynamic team that works closely with both relevant AstraZeneca stakeholders and Customers, providing regulatory and compliance advice/information as appropriate to ensure the compliant supply of product to Customers. You 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 upload, 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.
• 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 own projects are 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:

• Bachelor's degree in Science, Regulatory Sciences, Pharmacy, or Pharmaceutical Sciences.
• Basic knowledge of the regulatory submissions 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.

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.