Regulatory CMC Associate at AstraZeneca

Poolia Sverige AB, Poolia Life Science & Engineering AB / Kemistjobb / Södertälje
2016-01-29
Observera att sista ansökningsdag har passerat.
➡️ Klicka här för den senare publicerade platsannonsen "Regulatory CMC Associate at AstraZeneca" (publicerad 2016-03-11) ⬅️


Visa alla kemistjobb i Södertälje, Salem, Ekerö, Nykvarn, Botkyrka eller i hela Sverige
Visa alla jobb hos Poolia Sverige AB, Poolia Life Science & Engineering AB i Södertälje, Salem, Botkyrka, Sundbyberg, Stockholm eller i hela Sverige

On behalf of our client, AstraZeneca, we are now looking for a Regulatory CMC Associate for a temporary assignment in Södertälje.

The assignment which is full-time will as soon as possible with the duration of one year. Selections and interviews are held on an ongoing basis, so please submit your application as soon as possible. Cover letter and cv are preferred in english.

Job description
This role offers great opportunities for you to work with global networks, as a member of the CMC Regulatory Compliance organization within AstraZeneca. CMC Regulatory Compliance is a global function that manages all Chemistry, Manufacturing and Controls (CMC) post-approval regulatory activities across the global supply chain. The Regulatory CMC Associate generates CMC documentation presented in the required format to the agreed timetable, for worldwide submissions, i.e.:
• you will work with colleagues and other functions within AstraZeneca to obtain information that supports the generation of regulatory documentation.
• you may coordinate assembly of submission-ready documents to support lifecycle submissions.
• you will keep business wide electronic systems up to date to be consistent with regulatory submissions and commitments.

Qualifications
For this role we require that you have the following education and experience:
• university degree, or equivalent, in Chemistry, Pharmacy or Chemical Engineering
• IT software skills
• fluently spoken and written English and Swedish
• experience in Pharmaceutical Production or Quality Assurance or Quality Control or Product Maintenance or Regulatory Affairs

We also require that you have the following skills and capabilities:
• ability to work collaboratively with customers and colleagues to achieve optimum outcomes
• knowledge of information and document management technology and electronic/paper publishing software
• 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
• good communication skills

Varaktighet, arbetstid
100% Visstidsanställning

Publiceringsdatum
2016-01-29

Ersättning
Enligt överenskommelse

Så ansöker du
Sista dag att ansöka är 2016-02-08
Ange följande referens när du ansöker: 658868
Klicka på denna länk för att göra din ansökan

Kontakt
Joakim Karlsson

Företag
Poolia Sverige AB, Poolia Life Science & Engineering AB

Adress
Poolia Sverige AB, Poolia Life Science & Engineering AB
Kungsgatan 57 A, Box 207
10124 Stockholm

Kontorsadress
Kungsgatan 57 A, Box 207

Jobbnummer
2643376

Observera att sista ansökningsdag har passerat.

Prenumerera på jobb från Poolia Sverige AB, Poolia Life Science & Engineering AB

Fyll i din e-postadress för att få e-postnotifiering när det dyker upp fler lediga jobb hos Poolia Sverige AB, Poolia Life Science & Engineering AB: