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Client:Pharma Point
Location:Job Category:Other
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EU work permit required:Yes
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Job Reference:626398821096829747233711
Job Views:1
Posted:18.07.2025
Expiry Date:01.09.2025
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Job Description:For our client, a growing CDMO specialized in development and production of sterile injectable products, we're looking for a
BUSINESS DEVELOPMENT - PROJECT MANAGER - TECHNOLOGY TRANSFER The candidate, reporting to the BD manager, will lead and manage key projects with a primary focus on execution.
This includes managing stakeholder expectations on project scope, deliverables, and timing.




Product and business goals will be achieved by planning and directing project plans, managing cross-functional teams, and coordinating activities within established project timelines and budgets, with the following key responsibilities:
Project management: Manage CDMO projects (Technology Transfer and new Development) as SPOC with customers for all project aspects;Coordinate internal project activities, lead multidisciplinary teams, set up and lead project meetings, and issue Project Plans;Monitor adherence to timelines and costs;Provide regular updates to CCO and Management on project status;Support Finance in project cost controlling and updating financial WIPs;Coordinate external activities (e.g., laboratory activities) connected with project execution;Business Development: Manage new customers until product launch;Support CCO in technical evaluation of new projects;Prepare Technology Transfer and Commercial Proposals;Represent the company at international exhibitions and congresses;Support CCO in scouting for new customers and business opportunities;Manage in-licensing and out-licensing of new products;Assist CCO in budget proposals for new projects and products.New Products Launch: Coordinate activities to support the commercial launch of new products, ensuring material availability, proper documentation, and timely internal activities;Serve as SPOC with external customers for new product launches, setting up launch preparation plans;Regulatory: Coordinate regulatory activities, evaluations, and timelines for new projects, serving as SPOC with customers for regulatory documentation readiness.Qualifications:
Degree in Pharmacy, CTF, Chemistry, or Biotechnology;Knowledge of the pharmaceutical industry and CMO manufacturing processes;At least 3 years of experience in a complex multinational CMO environment;Formal project management training preferred;Positive attitude, driven, persistent, and results-oriented;Fluent in English (speaking, reading, writing);Excellent conflict resolution, negotiation, and problem-solving skills;Ability to influence others and reach agreements;Ability to work independently and in a team environment.
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