Project Leader - OTC New Product Development

To manage and provide oversight to a series of projects associated with New Product Development of OTC products within the EMEA region. The scope of a project is to plan, execute and monitor from its agreed definition to the first launch in the region. The projects will, to various extents, typically be connected to external partnerships.



The project management aspects would include, but not be limited to;

. Drive the technical aspects of the NPD

. Coordinate with internal and external teams the requirements to achieve goals of the projects

. Comprehensive technical due diligence reviews of external opportunities and licenses including risk assessments

. Technical transfers between development and commercial production facilities

. Ensure that correct technical documentation is available to support successful registration applications

. Generate project budget request, tracking approved budgets as well as appropriate financial monitoring and follow-ups.

You will be expected to be the primary contact for negotiating access to, and collaborate with, external and internal cross-sector resources to complete the projects in scope.

Business: Proffice Life Science AB

City: Helsingborg

Job type: Full time, long-term assignment

Deadline for applications: 2014.01.12

More information: Camilla Wern, 0733-436098

Qualification:

Minimum a Bachelors degree with a major in chemistry or pharmaceutics or an equivalent degree within related sciences.

Work Experience:

. A minimum of 5 years in a pharmaceutical manufacturing or product development environment with an emphasis on multi-ingredient solid-dose formulation. Especially, technical experience in Formulation and/or Analytical Development specifics is seen as favorable.

. Technical experience with non-prescription ingredients used in cough, cold & allergy preparations and analgesics is a distinct advantage. Experience with flavouring technologies is an advantage.

. Experience in technical project management of New Product Development preferably as lead, but also as team member, is seen as a merit.

. Comprehensive understanding of quality compliance knowledge within EU and good understanding of GxP systems.

. Strong back ground in Medicinal regulation, but also experience in Medical Device and/or Food Supplement regulations in the EMEA environment is seen favorable.

. A demonstrated business partner and ability to bring together multi-disciplined technical staff in order to work with problem solving.

. Technical writing and documentation review abilities.

. Demonstrable experience of working with external development partners and manufacturers.

Please send your application in English and apply at our website www.proffice.se We put great emphasis on personal suitability for this role.

Organization/Business description:

Proffice Life Science is the leading Nordic specialist of temporary recruitment services within the Biotech and Chemtech industries. We are able to provide our Nordic clients with highly skilled and experienced specialists from all over Europe.

All consultants, employed by Proffice, are specialists. Proffice is one of the largest and most well-renowned staffing agencies in Sweden. All consultants, hired by Proffice, have secure and permanent employment contracts with a certified staffing agency. We offer excellent benefits and personal developmentopportunities within a wide range of positions and industries.

Our clients expect only the best from Proffice and we expect only the best from our consultants. As you will spend your working day on our clients' premises, you will have to not only be an expert in your field, but also a flexible, independent and social member of the team. You thrive on new challenges and welcome new opportunities. If this appeals to you, we offer a stimulating job, with excellent benefits such as private medical insurance, discounted gym membership and further contributions to health care related activities.

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