3PS CMC Associate to AstraZeneca in Södertälje

Randstad Life Sciences is now looking for candidates for a consultant assignment as 3PS CMC Associate at AstraZeneca in Södertälje. The assignment is planned to start in august and is planned to last until 2020-07-30.
Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

About AstraZeneca

At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality.
At AstraZeneca, innovation is about more than just research. We aim to stimulate continued creativity throughout our organisation by maintaining a culture in which our people feel valued, energised and rewarded for their ideas and contribution to our success - ideas which can make a difference in all aspects of our business.


AstraZeneca is operating as a supplier for divested products where the manufacturing licence is now owned by an external partner. As part of this relationship there is a requirement to ensure that AstraZeneca manufacturing network has full visibility and access to the current regulatory approved Chemistry Manufacturing and Controls (CMC) dossier for each country where the product is marketed. This is critical in ensuring that products are manufactured in compliance with the licences held by the third party licence holder.


Whilst this role is based in Gärtuna, you will join a team of Regulatory system specialists within a global Operations Quality function based both in Gärtuna and Macclesfield, UK.


You will liaise with internal Regulatory specialists and external partners and be responsible for the upload of CMC documents into a document management system. Compliance with established good documentation practices such as version control, ensuring business approval and document format will be part of this work. Communication of any changes to this information, such as new market approved documents, to the relevant manufacturing sites is also a critical success factor.

Additionally, you will be required to ensure that AstraZeneca's change control system is maintained to reflect regulatory assessments supplied by the third party. You will responsible for the upload of documents provided by external partners and for communication to relevant manufacturing sites.

You will be part of the 3PS Quality network and act as a key contact person for ensuring dossier visibility.

You will be expected to work alongside another 3PS CMC associate participating in the improvement of processes required to achieve the above.


Essential requirements:

  • Educated to degree level
  • Strong IT skills, experience of document management systems preferable
  • Self motivated and capable of working under minimal supervision
  • Excellent communication skills (written and oral)
  • High level understanding of GMP and working in a regulated environment
  • High level understanding of CMC Regulatory CMC knowledge
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 or any other characteristic protected by law.

Business: Randstad Life Sciences

City: Södertälje

Job type: Full time

Deadline for applications: 2019-06-14

More information: Sofie Önnestam, [email protected], 073 343 99 61

Please send your application in English.

We encourage you to send your application as soon as possible, since interviews and candidate selection are done continuously! We put great emphasis on personal suitability for this role.
Organization/Business description:

Randstad Life sciences is specialized in recruitment and consulting providing competences within Life Science, Science and Engineering and is a company where people make all the difference. At Randstad Life Sciences specialists are recruiting specialists!

All our recruitment consultants , consultants and sourcing managers have a technical or scientific background, combined with extensive networks within relevant communities and expertise within recruitment and HR. We understand our customers specific requirements and know how to find the best candidates. Through our passionate commitment and high degree of attentiveness we help people and businesses to grow and be competitive in a changing world.