Merge sub-team plans and schedules into a master IDST project schedule and ensure all cross functional efforts are aligned with target milestones.
Monitor the achievement of progress compared to plans via engagement with sub-teams and key support functions. Monitor activities to ensure all functions are adequately supporting project objectives and timeline. Assist in compilation of metrics and progress updates.
When necessary, integrate multiple projects and programs to identify constraints/opportunities.
Support scheduling, facilitation, and note-taking for team meetings.
Support compilation of cross-functional data summaries and report-outs. Examples include resource forecasting and financial/budgeting compilations.
Support assessments of project-level risks for schedules and resources to assign preventive action plans and identify the needs for escalation.
Serve as knowledge management steward for the program and owner of the knowledge management database. Support team to ensure consistent and effective use of knowledge management tools.
Assist with other administrative tasks or business process improvement initiatives as needed.
The Ideal Candidate would possess:
Experience in drug development or manufacturing (e.g., operations, technical support, supply chain), is highly desirable.
Professional Project Management certification (e.g., PMP) or past work experience in project management role is desirable.
Experience with the planning and execution of strategies for drug and/or vaccine product registration, pharmaceutical tech transfer and CMC, and/or life-cycle management (can be R&D, manufacturing, or commercial perspective).
Strong interpersonal skills. Able to proactively engage others to obtain the desired information and outcome.
Strong written and oral communication skills.
Demonstrated ability to create and analyze detailed, cross-functional project plans (including Gantt charting), and manage execution and change against those plans.
Ability to succeed in a dynamic environment; flexibility to respond to changing priorities.
Minimum Qualifications:
Bachelor's degree in Science, Engineering, Project Management, or business related discipline.
A minimum of 2 years of relevant job experience
Authorization to work in the United States indefinitely without restriction or sponsorship
What we offer:
Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Position is full-time, Monday through Friday, 8 a.m. to 5 p.m., with the ability to flex hours as needed to support manufacturing. Position will support manufacturing operations, therefore weekend and holiday work may be necessary. Candidates currently living within a commutable distance of West Point, PA are encouraged to apply.
Eurofins Lancaster Laboratories Professional Scientific Services ® (PSS) is a global, award-winning insourcing solution that places our people at our clients' site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client's quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com .
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
