Associate Project Management

Description:
Note:
Can sit anywhere in US and work the business hours in their time zone. Please list location on resume.

**Nice to Have- Smart sheets, raw materials, Pharma or biotech experience.** Less than a year at a prior employer is a red flag.

Role and Responsibilities
Manage multiple cross-functional raw material onboarding, life cycle management, and operational excellence projects of medium to high complexity to ensure raw material supply assurance.
Oversee the activities of all operations aspects involved in onboarding and operational excellence projects to ensure raw material supply assurance.
Partner with internal and external cross functional teams, manage onboarding related meetings, minutes, action items, escalations and drive decision making process
Coordinate creation of/updating and archiving of onboarding related documents
Project management of resource planning, generating and reporting metrics/ KPIs and presentation materials for management reviews and governance meetings
Responsible for building project plans and team assignments using Gantt charts, estimating project cost and adhering to budget, directing and monitoring work efforts daily, identifying resource needs, performing business quality reviews, and escalating functional, quality, timeline and cost issues appropriately.
Utilize project management processes, software andal Excellence (OE) to ensure optimal execution of projects and continuous improvement initiatives.

Preferred Experience methodologies to ensure projects are delivered on time, within budget, adhere to high quality standards and meet internal and external customer expectations.
Coordinate communication with all areas of the enterprise that impact scope, budget, risk and resources of the work being managed.
Lead continuous improvement projects that deliver measurable gain in quality, efficiency and alignment within Amgen. Apply the knowledge, skills, tools of project management / Operation

• Managed and led medium to complex projects, comfortable with change and uncertainty.
• Extensive knowledge and expertise in the use of project management methodologies and tools, resource management practices and change management techniques
• Knowledge of business principles, product development and commercialization or RD in a life science, pharmaceutical, biotechnology, medical device cGMP environment.
• GMP environment work experience and thorough understanding of biological/chemistry technology transfer processes and timelines
• Strong analytical skills and knowledge of tools within MS Office, MS Project, Smartsheet, ThinkCell, and other software programs
• Excellent leadership, interpersonal skills, and influencing skills vertically and horizontally with integrity. Process oriented with business acumen.
• Strong organizational skills, strategic networking, self-motivation, collaboration and flexibility.
• Excellent interpersonal, verbal communication and writing skills
• Has demonstrated the courage and ability to solve technical problems and challenges in Teams.
• Has proven communication skills (presents confidently and convincingly at all level of the organization).
• Expert skills in lead and managing people and teams management of diverse cultures and geographic locations, conflict resolution with diplomacy.
• Ability to work in a fast paced, dynamic environment

Top 3 Must Have Skill Sets:

• Excellent leadership, interpersonal, verbal communication and writings kills
• Strong organizational skills, strategic networking, self-motivation, collaboration and flexibility.
• Ability to work in a face pace and adapt to priority changes

Pay Rate between $46- $52/Hr on W2 based on experience.

"This posting is for Contingent Worker, not an FTE"

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