Regulatory CMC Associate to AstraZeneca

Regulatory CMC Associate to AstraZeneca

Arbetsbeskrivning

On behalf of our client, AstraZeneca, Poolia Life Science is now looking for a Regulatory CMC Associate for a consultant assignment with start as soon as possible until 31/12/2021. Selections and interviews are held on an ongoing basis, please submit your application as soon as possible.

Operations Regulatory is a global function that manages all Chemistry, Manufacturing and Controls (CMC) post-approval regulatory activities across AstraZeneca’s global supply chain. We are looking for Regulatory CMC Associates to our product teams located in Södertälje.

We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join us and be part of an extraordinary place to work; an environment that energizes and empowers each of us to support compliant product supply through partnership with other AZ teams.

THE ROLE
As a Regulatory CMC Associate you will generate CMC documentation to support lifecycle submissions and keep business wide electronic systems up to date to maintain regulatory status up to approval of CMC documentation supplied by Operations to Global Regulatory Affairs.
You will work with colleagues and other functions within AstraZeneca to obtain information that supports the generation of regulatory CMC documentation.

You may also support externalisation projects and transfer of CMC documentation to external partners.


MINIMUM REQUIREMENTS - EDUCATION AND EXPERIENCE
• Degree in Chemistry or Pharmacy or Chemical Engineering
• Fluently spoken and written English and Swedish
• Experience in Post Approval Regulatory CMC including CMC documentation authoring
• Experience in Pharmaceutical Production or Quality Assurance or Quality Control or Product Maintenance or Regulatory Affairs


SKILLS AND CAPABILITIES
• Able to work collaboratively with customers and colleagues to achieve optimum outcomes
• Knowledge of information and document management technology
• IT software skills
• Ability to work with short and / or changing timelines
• Attention to details, highly organized, able to plan and control own workload effectively and manage expectation of others
• Excellent written and verbal communication skills
• Experience from using Document Management systems



Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered.

Poolia is a registered staffing agency, meaning that we comply with the requirements set by Kompetensföretagen - the Swedish Association of Staffing Agencies.

Kontaktpersoner på detta företaget

Sara Jupiter

Emma Bergman
08 555 540 09
Natalie Squalli

Margot Estlander
08-555 651 24
Margot Estlander

Karl Engström

Margot Estlander
08 555 651 24
Joacim Jonasson
08 555 651 26
May Molin
08-55565017
Joacim Jonasson
08-555 651 26

Sammanfattning

  • Arbetsplats: Poolia Life Science & Engineering AB
  • 1 plats
  • 6 månader eller längre
  • Heltid
  • Fast månads- vecko- eller timlön
  • Publicerat: 26 februari 2021
  • Ansök senast: 3 mars 2021

Besöksadress

Box 207, Stockholm
None

Postadress

Box 207
Stockholm, 10124

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26 november 2024