Overview
On Site
Full Time
Skills
Performance Management
Preventive Maintenance
Pharmaceutics
English
Software Project Management
Technology Transfer
Cross-functional Team
Packaging Design
Test Methods
FOCUS
Data Flow
GMP
New Product Introduction
Documentation
Project Planning
Dashboard
Communication Planning
Engineering Management
Science
Collaboration
Teamwork
Communication
Manufacturing
Product Design
Project Scheduling
Risk Assessment
Management
Project Management
Job Details
Onsite Ohio - 5 days a week.
Schedule is typically 8am - 5pm (some flexibility with schedule, may be expected to work OT 10% of the time during peak season).
Ideal Candidate: Experience: Biotech and pharma, GMP environment, manufacturing and tech transfer background, combination products.
Skills: Strong English written and verbal communication skills, MS Office, SmartSheet (project scheduling software), project management experience in a supporting role.
Desired: Engineering Background.
Key Responsibilities:
In this dynamic role, you will organize Technology Transfer activities for Final Drug Product (FDP) manufacturing.
Responsibilities include supporting and creating project schedules, lead site assessment and manufacturing capabilities, update project dashboards, and leading team meetings to progress the project towards final objectives. You will work across a global, cross-functional team consisting of manufacturing, device and packaging design for combination products, capital projects, physical test methods, quality, and regulatory team members.
Your role will focus on leading effective Tech Transfer projects for combination products, enhancing end-to-end controls with robust methods and data flow in a GMP setting.
Supporting New Product Introduction to Client manufacturing site.
Owning documentation such as Project Plan, supporting engineering with Process Transfer Documents (PTD), protocols, and reports.
Supporting engineers with Make-a-Batch (M-a-B) activities to ensure sending/receiving site expectations are met.
Developing, tracking, and providing project dashboard updates.
Providing good communication plans to cross-functional teams and Process Engineer management.
Ability to apply project management and engineering science to production.
Strong teamwork and excellent interpersonal and communication skills.
Basic Qualifications:
Master's degree
OR Bachelor's degree and 2 years of experience
OR Associate's degree and 6 years of experience
OR High school diploma/GED and 8 years of experience
Preferred Experience:
Experience in the Tech Transfer of Combination Product field, focusing on project management and/or manufacturing.
Understanding of interdependencies of complex projects, especially involving new product introductions with new equipment/processes.
Knowledge of Combination Product design controls and regulatory requirements on a global scale.
Familiarity with Client's commercialization framework.
Program and Project Management skills (experience with MS Project, SmartSheets, and other project scheduling software is desired).
Additional Skills:
Proactive risk assessment, management, and mitigation.
Ability to lead and succeed in an ambiguous environment.
Strong project management skills.
Schedule is typically 8am - 5pm (some flexibility with schedule, may be expected to work OT 10% of the time during peak season).
Ideal Candidate: Experience: Biotech and pharma, GMP environment, manufacturing and tech transfer background, combination products.
Skills: Strong English written and verbal communication skills, MS Office, SmartSheet (project scheduling software), project management experience in a supporting role.
Desired: Engineering Background.
Key Responsibilities:
In this dynamic role, you will organize Technology Transfer activities for Final Drug Product (FDP) manufacturing.
Responsibilities include supporting and creating project schedules, lead site assessment and manufacturing capabilities, update project dashboards, and leading team meetings to progress the project towards final objectives. You will work across a global, cross-functional team consisting of manufacturing, device and packaging design for combination products, capital projects, physical test methods, quality, and regulatory team members.
Your role will focus on leading effective Tech Transfer projects for combination products, enhancing end-to-end controls with robust methods and data flow in a GMP setting.
Supporting New Product Introduction to Client manufacturing site.
Owning documentation such as Project Plan, supporting engineering with Process Transfer Documents (PTD), protocols, and reports.
Supporting engineers with Make-a-Batch (M-a-B) activities to ensure sending/receiving site expectations are met.
Developing, tracking, and providing project dashboard updates.
Providing good communication plans to cross-functional teams and Process Engineer management.
Ability to apply project management and engineering science to production.
Strong teamwork and excellent interpersonal and communication skills.
Basic Qualifications:
Master's degree
OR Bachelor's degree and 2 years of experience
OR Associate's degree and 6 years of experience
OR High school diploma/GED and 8 years of experience
Preferred Experience:
Experience in the Tech Transfer of Combination Product field, focusing on project management and/or manufacturing.
Understanding of interdependencies of complex projects, especially involving new product introductions with new equipment/processes.
Knowledge of Combination Product design controls and regulatory requirements on a global scale.
Familiarity with Client's commercialization framework.
Program and Project Management skills (experience with MS Project, SmartSheets, and other project scheduling software is desired).
Additional Skills:
Proactive risk assessment, management, and mitigation.
Ability to lead and succeed in an ambiguous environment.
Strong project management skills.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.