Regulatory Project Manager to AstraZeneca Gothenburg

Jurek Rekrytering & Bemanning AB / Byggjobb / Göteborg
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Jurek Rekrytering & Bemanning erbjuder ett komplett utbud av bemannings- och rekryteringstjänster. Vi rekryterar och hyr ut alltifrån studenter till yrkesverksamma akademiker med mångårig erfarenhet och specialistkompetens. Våra uppdrag är främst inom juridik, ekonomi, HR, marknad och administration.

Jurek Rekrytering & Bemanning AB is a niche company in recruitment and staffing within law, finance, marketing, administration and HR. Our clients include the biggest companies in Sweden, as well as government authorities and many medium-sized and small enterprises. Basically, we are able to offer all types of job and position.

Astra Zeneca is now looking for a Regulatory Project Manager to AstraZeneca Gothenburg for a consulting assignment at AstraZeneca, with start in the end of September for a temporary position to September 2019. Thus, you will be employed by Jurek Rekrytering & Bemanning. If questions you are very welcome to contact recruitment consultant Tilda Dahlberg at tilda.dahlberg@jurek.se, or + 31-712 83 48

Regulatory Project Manager to AstraZeneca Gothenburg

AstraZeneca is a science-led, global biopharmaceutical company, with a focused portfolio in core therapies. We are committed to improving the health and lives of people across the globe, through our broad research and development platform, and a growing late-stage pipeline. Working in over 100 countries, we have strength in most global markets. Our medicines are used by millions of patients and clinicians worldwide.

The arena

The Regulatory Project Management (RPM) is a group within the AZ Global Regulatory Affairs, Patient Safety and QA (GRAPSQA) organization. RPM is accountable for end to end regulatory submission delivery, providing regulatory expertise, efficient project management and strong leadership in line with business priorities. The RPM is allocated to project teams with the responsibility to plan, prepare and deliver various types of regulatory submissions.

We now have a temporary position in our team for one year.

Accountabilities/Responsibilities:

* Project manage (plan, prepare, coordinate and deliver) submission in accordance with agreed plans.
* Develop, execute and maintain submission plans and proactively provide status updates to designated stakeholders.
* Identify potential regulatory risks to the operational plans and propose options to mitigate these. If required, lead sub-teams to deliver regulatory submissions.
* Provide operational regulatory input and guidance with respect to regulatory submissions.
* Ensure that appropriate, up-to-date records are maintained for compliance.
* Use and share best practices, when handling various applications and procedures.

Preferred skill/experience:

* University Degree in Science or related discipline
* Project Management experience
* Relevant regulatory experience or experience elsewhere in Pharmaceutical Industry
* Knowledge of the drug development process
* Excellent written and verbal communication skills
* Global team experience

Varaktighet, arbetstid
Heltid Visstid

Publiceringsdatum
2018-07-03

Ersättning
Fast lön

Så ansöker du
Sista dag att ansöka är 2018-08-14
Klicka på denna länk för att göra din ansökan

Kontakt
Tilda Dahlberg

Företag
Jurek Rekrytering & Bemanning AB

Adress
Jurek Rekrytering & Bemanning AB
Biblioteksgatan 11
11146 Stockholm

Kontorsadress
Biblioteksgatan 11

Jobbnummer
4236316

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