Principal Scientist

Patheon

(Greenville, North Carolina)
Full Time
Job Posting Details
About Patheon
We believe the world would be a healthier place if tomorrow's medicines were made available today. Patheon is transforming the way pharmaceuticals are made with a simplified, end-to-end supply chain solution for pharmaceutical and biopharmaceutical companies of all sizes. Drug substances and drug products. Development and manufacturing.
Summary
Recognize, develop and implement new technologies and methods supporting the drug product development process to fulfill client and regulatory requirements. Serve as primary technical expert for project teams and lead and coordinate activities to ensure successful completion of projects. Perform management duties during group leader’s absence, including prioritizing all project activities, maintaining support of development schedules, and coordinating technical staff. Train junior staff. Internal departments - Develops, plans and executes change activities. Supports corporate projects: Lean Six Sigma and Compliance initiative. Customers - Tour; screening projects; work with New Business Development . Provide technical support to customers.
Responsibilities
* Design, validate and/or implement new dosage forms/analytical methodology including the development of production processes, including all necessary procedures, training, and regulatory documentation * Participate on project teams as member, leader, or liaison to facilitate the team’s activities and achievement of goals. * Recognize potential process improvements, recommend associated actions, and develop and implement appropriate solutions * Serve as primary technical expert for related job area for all areas of the company and its’ associated partners. * Manage and coordinate group activities to meet specified departmental and corporate goals and timeframes. * Effectively interpret and defend dosage form/analytical data and reports and interact with Regulatory Affairs in response to official inquiries * It is the responsibility of each employee to work in a safe and responsible manner in order to create an injury-free and incident-free workplace.
Ideal Candidate
* BS/BA in a physical or biological science with 5 years experience in manufacturing, process development, laboratory, or technology transfer. * AA/AS in a physical or biological science or production related discipline plus 6 years experience in manufacturing, process development, laboratory, or technology transfer. 7 years experience in manufacturing, process development, laboratory or technology transfer * Demonstrated creativity in designing novel solutions to complex technical problems and expertise in development approaches as applicable to area. * Ability to collaborate with co-workers and clients to meet goals. * Strong knowledge of domestic and international regulatory requirements and pharmaceutical manufacturing processes.
Compensation and Working Conditions
Reports to Regulatory Affairs

Questions

Answered by on
This question has not been answered
Answered by on

There are no answered questions, sign up or login to ask a question

Want to see jobs that are matched to you?

DreamHire recommends you jobs that fit your
skills, experiences, career goals, and more.