Regulatory CMC Associate to AstraZeneca, Södertälje

Do you have a degree in Chemistry, Pharmacy or Chemical Engineering? Do you want to generate CMC documentation to support lifecycle submissions and keep business wide electronic systems up to date? At Experis Engineering we are now looking for a Regulatory CMC Associates for a consultancy assignment to AstraZeneca in Södertälje. Read more about the position below and welcome with your application!

Location: Södertälje
Start date: 1 January 2021
Assignment: Consultancy assignment until 31 december 2021

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

AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.



What we can offer

As a consultant at Experis you get the opportunity to develop your knowledge within different fields at some of Sweden's leading companies. At Experis we are very proud of our consultants and together we find the right challenges for you. We have high expectations on you but in return we offer you great possibilities to grow and make a career.



Apply today!

You apply for this position only with registered or attached resume. We do not accept applications via email. If you have any questions regarding this position please don't hesitate to contact Talent Acquisition Specialist Paula Skoglund at Paula.Skoglund@se.experis.com

The selection will be ongoing, therefore apply as soon as possible.

Welcome with your application!