Senior Project Manager

LANNETT COMPANY, INC; Seymour (IN); On-site; USD 110,000 - 140,000; Full time

Job summary

LANNETT COMPANY, INC is seeking a Senior Project Manager to lead multiple concurrent projects in a pharmaceutical manufacturing environment. You will coordinate cross-functional teams to plan, execute and deliver projects from early development to commercial launch, including product transfers and CDMO related work.

The role requires advancing project plans, mitigating risks, and maintaining status updates for senior management, with leadership in meetings and collaboration across internal and

Qualifications

• Bachelor’s degree in scientific, engineering, business, project management or related discipline.
• 10+ years of project management experience in pharmaceutical manufacturing.
• Experience coordinating cross-functional projects across multiple departments.
• PMP certification preferred but not required.
• Strong leadership and communication skills.

Responsibilities

• Leads and coordinates multiple complex projects, managing scopes, schedules, and budgets.
• Develops and communicates project plans and tracking tools to stakeholders.
• Initiates new projects, sets timelines, coordinates meetings, and resolves obstacles to ensure on-time completion.
• Manages deficiency tracking and gap analysis for unapproved products to support regulatory approvals.
• Facilitates team meetings, tracks action items, and communicates milestones and milestones with management.
• Tracks contract milestones, obligations, and payments when applicable.

Skills

FDA regulatory knowledge

MS Project

Project management

Cross-functional collaboration

Leadership & communication

Education

Bachelor's degree

Tools

MS Project

MS Teams/Planner

Job description

Description

The Senior Project Manager is responsible for leading and coordinating multiple concurrent projects within a pharmaceutical manufacturing environment. This role partners with cross-functional teams across multiple departments to plan, execute and deliver projects timely that support business objectives. Projects will range from early product development through commercial launch; product transfers, special projects, and CDMO projects through launch. The Senior Project Manager coordinates the resources required for successful project completion, identifies and removes roadblocks, and maintains project tracking tools to provide up-to-date project status as required.

• Leads and manages multiple complex projects simultaneously, including oversight of project scopes, schedules, budgets while identifying proactively identifying and removing roadblocks.
• Develops, manages and communicates project plans and other company tracking tools

Communicates project objectives, deliverables, timelines and tasks to cross functional team members

• Work with project stakeholders to initiate new projects, set timelines, coordinate meetings, identify and help to resolve obstacles, and elevate issues when necessary to support resource allocation and on-time project completion
• For unapproved products, manage the deficiency tracking system and gap analysis program to ensure that action items are completed on time to support timely approvals
• Demonstrate leadership qualities while facilitating team meetings to ensure the agenda is followed, coordinate follow-up on action items
• If applicable, proactively track, monitor and communicate contract milestones, obligations and any financial payments to project team leaders and management.

Proactively identify project risks and assist in developing mitigation strategies. Communicate both positive and negative impact to the project.

If applicable, support Director in partner collaborations and attend business review meetings.

Requirements

Experience

• Bachelor’s degree in scientific, engineering, business, project management or related discipline.
• Minimum of 10 years of project management, preferably within pharmaceutical manufacturing.
• Experience coordinating projects involving multiple functional departments and organizational levels.
• PMP Certification preferred but not required

Skills

• Understanding of FDA regulatory development and submission processes
• Proficiency with MS Office Programs, including MS Project and MS Teams/Planner
• Proven ability to manage multiple, multi-faceted projects and deliver results
• Experience working with multidisciplinary groups (internal & external) and ability to work in and communicate across all levels of the organization
• Leadership, negotiation, presentation and facilitation skills

Ability to work with minimal supervision to meet required timelines