(Senior) Analytical Project Manager

Fuldtid

Permanent

Novo Nordisk Park 1, 2760 Måløv, Danmark

ID: 2558006

Indrykket for 33 dage siden

Do you want to drive and impact a variety of early and late-stage drug product development projects? Are you ready to apply your project management experience and analytical development skills in an exciting organization, where you will get challenged, grow, and expand your capabilities to the fullest? And do you want to join a dynamic and highly competent analytical project team?

We are looking for multiple Experienced Analytical Project Managers, at Principal Scientist/specialist level, to support within various fields of our development portfolio. Could be within molecular biology techniques, small/large molecules and/or oral/injectable drug products.

Apply now if you have the relevant project management and analytical development skills.

The position

You will interact with a wide variety of stakeholders such as Analytical departments, Production, Quality Assurance and Regulatory Affairs.

As (Senior) Analytical Project Manager you will be responsible for:

Analytical development and characterization activities and strategies for drug substance and drug product, through project management

Driving the projects through the different stages of clinical development and collaborate within CMC Development and with our colleagues in Product Supply as well as other areas of the R&D organization or contract manufacturers

Leading the analytical project team in an engaging and motivating way and participate in writing and compiling regulatory applications and various internal and external documentation

Coordinating the transfer of analytical methods from our research unit to CMC Development & Scaling and further on to our manufacturing unit Product Supply or to a contract manufacturer

Communicating and coordinating with stakeholders within and outside CMC Development

Apart from that, you will be a member of the CMC Project Core Team where you will be responsible for planning and coordinating development activities within your expertise area and ensure deliveries according to the project plan.

Qualifications

You will be a great asset to our department because you have:

Extensive experience in leading analytical activities in either early phase and/or late phase clinical development.

Experience in managing and executing smaller and larger projects.

Scientific experience within analytical development, experience with regulatory submissions and perhaps experience in working with Contract Manufacturing Organisation (CMO).

A relevant academic degree within Pharmacy, Chemistry, Biology, Engineering, or a similar field.

Full professional proficiency in English

Have a high level of energy to drive activities and engage your colleagues forward

Apart from that you are result-oriented, take pride in delivering on your milestones, and motivate your colleagues with a positive, forthcoming attitude. You work well independently, although you should also be motivated to cooperate with colleagues and stakeholders across functions and departments.

Travel may occur in this role e.g. in relation to CMO collaborations. Will depend on assigned projects but expected 5-15 days per year.

About the department

Your new department, CMC Drug Product & Analytical Development - Project Office, consists of app. 50 employees located in Måløv. The department is involved in early and late-stage drug product development, analytical development and chemical and biological characterization of new entities moving through the clinical phases of drug product development.

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