IDMP Project Manager

Are you looking for an interesting challenge as Project Manager? Do you want to develop your carrier in one of the biggest pahrmaceutical companies? Do you have experience in regulatory environment and have worked in the pharma industry?

For our Client from the pharmaceutical industry we are looking for an

IDMP PROJECT MANAGER

Duration: 11 months

Location: Basel

Job purpose:

Work closely with the IDMP Project Lead to support the development strategy and implementation of the ISO IDMP (Identification of Medicinal Products) project across Franchises/BU/Divisions according to regulatory requirements

Major Accountabilities:

- As a member of the Regulatory Stategy & Intelligence (RS&I) Worksteam contribute to the action plan to implement ISO IDMP standards within the company
- Contribute to the System Delivery and Data Migration Workstreams to ensure activities are on-track and meet IDMP requirements in the new RIM system
- Contribute to the review of draft ISO IDMP requirements/guidance documents with internal alignment
- Works with relevant Line Functions to communicate ISO IDMP requirements by providing training sessions to RA colleagues, COs or X-functionally and via written communication such as Newsletters, information e-mails, etc.
- Support process changes at global and local levels to ensure compliance with HA requirements (planning, compilation, publishing and submissions to HAs according to the right format)
- Work with external Business Consultancy according to company needs

Ideal Background:

- Life Science Degree (eg Chemistry, Pharmacy, Biology), or MBA (Project Management)
- Fluency in English as a business language. Additional language is an asset
- Some experience in leader roles
- 3-5 years in Pharmaceutical Industry mainly in a regulatory environment and closely related areas (eg Clinical Development, GxP, Regulatory CMC, QA, Project Management)

If you are interested, please do not hesitate to apply:

Monika Bartosiewicz

(see below)