Senior Project Manager
Onsite Requirement
100% onsite
Location
On-site, Philadelphia
Position Id
2493
Recruiter Contact
LES
Job Description
Senior Project Manager
The Sr. Project Manager is responsible for managing integrated development and chemistry, and manufacturing programs of key clients while ensuring alignment with company’s functions, goals, and values. The Sr. Project Manager manages the planning, scheduling, and budgeting of CMC-related product/process development activities, including new product development, analytical methods development/validation, process improvements, and product characterization. In addition to managing key programs and their client relationships, the Sr. Project Manager will also support the development of the PM organization through coaching and guidance.
Responsibilities
- Create project plans to meet client needs.
- Track, adjust and report milestone deliverables to clients, as well as internally to the Director of Program Management, Site Leadership, and Executive Leadership.
- Communicate all changes, plans, and goals to partnering departments and functions.
- Assist with risk and mitigation planning.
- Create kick-off meetings and Joint Team Meeting (JTM) content, agenda, and minutes.
- Document agreements and any changes to the statement of work.
- Complete ERP system activities, invoicing, cost control, revenue recognition, material tracking and procurement and assist with forecasting and change management activities.
- Provide support with project budgets, including but not limited to: review cost/price analysis’, pressure test and align assumptions in the forecast, ensuring transparency and communication of the approved plan and funding status of activities.
- Assist with the development of others in the PM organization by providing coaching and guidance.
- Identify and support PM improvement initiatives.
- Provide support for the transfer of services between sites.
- Assist the PM Director in managing the PM group’s day to day tasks.
- Maintain positive personnel and client relationships and communication.
- Operate to the highest ethical and moral standards and participate effectively as a team player in all aspects of company’s business and adhere to quality standards set by regulations and company policies, procedures, and mission.
- Other related duties as assigned.
Qualifications/ Skills Required:
- MS in Life Science, Engineering or related field.
- 5+ years CMC experience in small molecules, biologics and broad knowledge of all aspects of CMC including process development, regulatory and quality requirements, analytical development, formulation and drug product technologies.
- 5+ years project management experience, leading multiple complex projects/programs
- Minimum of 3 years' experience in a client facing position.
- Knowledge of project management best practices and proficiency with supporting project management tools.
- Excellent written and oral communication skills in both individual and group settings.
- Excellent analytical, negotiation and problem-solving skills
- Demonstrated ability to organize, lead, and execute a variety of assignments and action plans.
- Experience working with key stakeholders.
- A solid understanding of CMC development milestones from Phase 1 to commercialization.
- Knowledge of finance, accounting and managing budgets.
- Current industry knowledge of relevant regulations, guidelines, policies and CMC requirements.