Analytical Lab, Project Analyst

Description

• Works with internal and external team resources to drive completion of project milestones, as determined by the team, based on timelines and project goals through all stages of the project.
• Develops technical knowledge, requires working knowledge and experience in project management.
• Manages single workstreams locally/globally and may work across multiple workstreams.
• Maintain clear communication paths with stakeholders.
• Leads projects with moderate resource requirements, risk, and/or complexity to achieve milestones and objectives.
• Solves complex problems by taking a new perspective using existing solutions.
• Drives transparency of project workloads, financial, commitments, and expectations.
• Maintains the project related data within the West Project Management System.
• Monitors resource needs and issues, work closely with resource managers to develop action plans to ensure project commitments remain on track.
• Manages project dependencies, escalating to the functional PMO as needed.
• Analyzes, Forecasts and Reports the project budget.
• Ensures projects are planned properly, including financials, resourcing, scheduling, and the business case, in support of quality deliverables.
• Defines, drives and manages change management and communications activities that support assigned projects.
• Champions the functional process and methodologies as applicable to projects/project teams.
• Executes on departmental strategy.
• Performs other duties as assigned based on business needs.
• Compiles KPIs and metrics from across all Quality Projects and reports on the data.

Qualifications

• Bachelor's Degree in Chemistry, Biology, Engineering or other related field, preferred.

Work Experience

• 3+ years GMP industry experience required.
• Knowledge and experience within their pharmaceutical/devices and general knowledge of related areas of project management preferred.
• Knowledge of GMP requirements and demonstrated experience managing projects in the medical device and pharma manufacturing industries; knowledge of applicable federal and international regulations preferred.

Preferred Knowledge, Skills And Abilities

• Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description.
• Able to comply with the company’s quality policy at all times.