CMC Regulatory Affairs Associate

Hays Specialist Recruitment AB / Biomedicinjobb / Södertälje
Observera att sista ansökningsdag har passerat.


Visa alla biomedicinjobb i Södertälje, Salem, Ekerö, Nykvarn, Botkyrka eller i hela Sverige
Visa alla jobb hos Hays Specialist Recruitment AB i Södertälje, Sundbyberg, Stockholm, Solna, Danderyd eller i hela Sverige

CMC Team

Hays Life Sciences is now looking to recruit a CMC Regulatory Affairs Associate to join the CMC team for a 12-month contract assignment with the possibility of extension at AstraZeneca in Södertälje.

CMC Regulatory Affairs is a global function that manages all Chemistry, Manufacturing and Controls (CMC) regulatory activities across AstraZeneca's global supply chain. We are looking for CMC Regulatory Affairs Associates to join our CMC team focused on divestment related activities 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 CMC Regulatory Affairs Associate you will generate CMC documentation to support lifecycle submissions and keep business wide electronic systems up to date to maintain regulatory status. You will support externalisation projects where transfer of CMC documentation to external partners is an important and regular task.

You will work with colleagues and other functions within AstraZeneca as well as external partners to obtain information that supports the generation of regulatory CMC documentation.

Minimum Requirements - Education and Experience

* Degree in Chemistry or Pharmacy or Chemical Engineering, or equivalent experience
* Fluently spoken and written English and Swedish
* Experience in Pharmaceutical Production or Quality Assurance or Quality Control or Product Maintenance or Regulatory Affairs

Skills and Capabilities

* Experience from and interest of using Document Management systems
* Attention to details, highly organized, able to plan and control own workload effectively and manage expectation of others
* Ability to work with short and / or changing timelines
* Able to work collaboratively with customers and colleagues to achieve optimum outcomes
* High level understanding of GMP and working in a regulated environment
* High level understanding of CMC Regulatory
* Excellent written and verbal communication skills
* IT software skills

Varaktighet, arbetstid
Heltid Temporary

Publiceringsdatum
2022-05-18

Ersättning
Not Specified

Så ansöker du
Sista dag att ansöka är 2022-05-28

Företag
Hays Specialist Recruitment AB

Arbetsgivarens referens
Arbetsgivarens referens för detta jobb är "900001".

Omfattning
Detta är ett heltidsjobb.

Arbetsgivare
Hays Specialist Recruitment AB (org.nr 556640-6103)

Ansökan
E-post: Hays.36800.3101@haysse.aplitrak.com

Arbetsplats
Hays Specialist Recruitment

Kontakt
Jay Mistry
matus@hays.pl
+46736425550

Jobbnummer
6657695

Observera att sista ansökningsdag har passerat.

Prenumerera på jobb från Hays Specialist Recruitment AB

Fyll i din e-postadress för att få e-postnotifiering när det dyker upp fler lediga jobb hos Hays Specialist Recruitment AB: