Medis

We are a company with extensive experience of generic pharmaceuticals who offers a broad portfolio of products and intellectual property to other pharmaceutical companies. We have a proven track record in securing regulatory approval prior to patent expiries and have obtained marketing authorizations in over 140 countries to date. Our company draws on the development and manufacturing capabilities of its parent company, Teva Pharmaceutical Industries Ltd. (NYSE and TASE:TEVA), whose R&D specialists maintain a strong development pipeline

Vinnustaðurinn

Launch Project Manager

The opportunity

The Launch Project Managers serve as an expert in B2B pharmaceutical launches and transfers. You will manage all aspects of a launch during the launch lifecycle (18 months), facilitate a timely launch and be responsible for project management of the transfers.

Helstu verkefni og ábyrgð

Collaborate with relevant internal and external stakeholders in order to create the optimal launch strategy for the customer and Medis.

Provide excellent service level to the launch/ transfer customers. This includes kickoff meetings, regular communication and timely feedback loop throughout the project lifecycle.

Communicating and cooperating with Teva production sites. This includes problem solving, support, prioritization and improvement/change management.

Gathering and maintaining information related to each launch and present the launch status during monthly meetings.

Setup and monitor the artwork process between the customer and the production site.

Setup and monitor the Quality Technical agreement process between the customer and production site.

Regular co-operation with the regulatory department on MA and variation status.

Setup and monitor the RCF process between the customer and the production site.

Maintain launch information in relevant launch systems e.g. SAP, Launch tracker, launch slides, CRM, SharePoint.

Menntunar- og hæfniskröfur

You will have a degree in a relevant discipline with previous project management certification and/or experience. It would also be beneficial if you have previous experience working with Regulatory Affairs / Business Development / Launch Management within the Pharmaceutical industry

You'll be confident communicating / presenting in English and be an independent, proactive person with strong problem solving skills

You'll need to have good numeracy and IT skills across Microsoft Office (particularly Excel and Word)

A team player who is used to working under pressure / to deadlines is also important

Auglýsing stofnuð15. september 2023

Umsóknarfrestur29. september 2023

Starfstegund

Staðsetning

Dalshraun 1, 220 Hafnarfjörður

Hæfni