We are currently looking for a talented R&D Project Manager. The successful candidate must have proven experience in CMC and formulation developments. The candidate must have good understanding of the product development process from formulation to registered batches manufacturing, and the regulatory requirements allowing successful registration with the authorities. Given that most of the new developments are targeted for the USA, experience with FDA requirements is a must.

The job description
As R&D Project Manager you will:
• Undertaking the full responsibilities for the CMC activities and for the development of products (planning, coordinating and supervising the activities of products developed by external centres and reporting their progress to the Management, other departments and partners), including leading and directing the formulation development,
• Ensuring that R&D department meets the timelines and manage delays, negotiate delivery time and cater efficient information flow between internal and external teams,
• Planning and negotiation of Project budgets and assessment of appropriate project scopes.

Your professional profile
• Strong educational background (MSc or higher in life science), course in Project Management is appreciated
• At least 10 years’ experience the pharmaceutical industry specifically in R&D department

Your abilities
• Strong interpersonal skills with the ability to influence others in a positive and effective manner,
• Demonstrated ability to contribute to a continuous learning and process improvement environment,
• Proven track record in product management or equivalent with knowledge of product management techniques and tools. Detail-oriented with the ability to proofread and check documents for accuracy and inconsistencies.
• Ability to understand and analyze scientific data and results and review scientific documents including drug development reports, publications and regulatory submissions.
• Strategic thinking, strong problem-solving and analytical skills
• Understanding the scientific principles and regulatory requirements
• Communication and motivation skills,
• Detailed oriented
• Strong sense of planning and prioritization
• Good understanding of and respect for cultural differences and the capacity to work effectively in a multicultural environment
• Fluent English, both written and oral

Hyloris is a virtual company focusing on launching added-value products in the US. The headquarter is in Liege, Belgium, but we have people based in the US also.
Hyloris has a robust management team with a success track record from many years in the pharmaceutical industry. We have a full operational structure with departments for Business Development, R&D, Regulatory, Medical Affairs and Licensing. Operations are currently outsourced.

Our values
Our talented staff work in accordance with our company values:
• We are proud of our entrepreneurial culture and foster open communication, mutual respect, professionalism and efficient decision-making and we believe that our multicultural organisation is one of our most important competitive advantages.
• We believe that timely and well considered decisions as a response to emerging opportunities and ideas is the key to our success.
• We believe that the success of the company lies in the competence, dedication and motivation of each of our employees.
• We believe that freedom returns flexibility and empowerment returns commitment.

We work on an exciting pipeline of more than 15 value added products and are focused on adding more projects to our pipeline, so we are heavily expanding the team. We are working with CDMO/CMOs World-wide.

For more information about our company, please visit www.hyloris.com. Motivation letter and CV can be sent to [email protected].

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