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Ascendia is a Contract Development and Manufacturing Organization (CDMO) company dedicated to enabling formulations for pre-clinical and clinical stage drug candidates and developing enhanced formulations of existing drug products. Ascendia specializes in creating formulations for poorly-water soluble molecules using nano-particle technologies. Ascendia assesses the feasibility of a broad array of formulation options in order to improve a drug’s bioavailability and solubility. Ascendia’s technologies include nano-emulsions, amorphous solid dispersions, nano-milling, injectable, lipid nanoparticles, and oral controlled release. Ascendia provides development, manufacturing and testing services - from discovery-stage molecules to life-cycle-management projects - creating formulation solutions with enhanced biopharmaceutical properties suitable for clinical scale-up.
The mission of our company is to provide customized formulation solutions to “salvage” difficult compounds and to create advanced medicines to help patients “prevail” over their disease and enhance quality of life.
We are looking for a highly skilled and detail-oriented
Assist with the creation and management of detailed project timelines, tracking milestones, and ensuring all deliverables are completed on time.
Coordinate project meetings, prepare agendas, ensure relevant stakeholders are invited, and take clear and concise meeting minutes. Follow up on action items to ensure timely completion.
Support the sourcing of materials, vendors, and other resources required for the project. Work with cross-functional teams to ensure the timely procurement of required resources.
Ensure that all project documentation is up-to-date and easily accessible. Track and report on the status of project deliverables, including any potential risks or delays.
Communicate regularly with internal and external stakeholders to provide updates on project status, resolve issues, and ensure alignment on project goals and timelines.
Monitor the project’s progress and performance, identifying and addressing any gaps or issues. Ensure all activities are compliant with industry regulations and quality standards.
Identify opportunities for process improvements and work with the team to implement more efficient project management strategies.
Ensure timely generation of scopes of work from existing clients garnering feedback from relevant stakeholders.
Bachelor’s degree in Pharmaceutical Sciences, Business, Project Management, or a related scientific field. PMP certification or equivalent is a plus.
1-3+ years of experience in pharmaceutical project management or a similar role, with proven ability to manage cross-functional teams and multiple projects simultaneously.
At Ascendia, we are passionate about improving patient outcomes, and we believe that every team member plays a crucial role in our success. We offer a collaborative work environment, opportunities for professional growth, and a comprehensive benefits package.
If you're an organized and proactive individual with a passion for project management in the pharmaceutical industry, we encourage you to apply! Please submit your resume and a cover letter to [email address] by [application deadline].
Ascendia Pharmaceuticals is an equal opportunity employer and strives to create an inclusive environment where all employees feel valued and respected.
Job Types : Full-time, Contract, Permanent
Pay : $60,000.00 - $90,000.00 per year
Benefits :Education :
Experience :
Ability to Commute :
Work Location : In person
Project Manager • North Brunswick, New Jersey, US