PRINCIPAL DUTIES:        

This position can be identified as a Project Manager II, III, or Senior based on the following: positive impact on the site and the organization and recognition of years of experience.

Client Management:

• Manage client satisfaction by managing client expectations efficiently with minimal coaching from Senior Manager Clinical Operations & Director, PDS Global Clinical Packaging Operations.  Maintain good working relationship with client.

Project Management:

• Manage clinical packaging projects with regular monitoring from Senior Manager/Associate Director, Clinical Project Management. 
• Develop and implement packaging/labeling strategies; Coordinate operational activities
• Ensure high quality documentation; Design clinical labels utilizing a computerized clinical trial labelling system
• Make sound judgments and recommendations on clinical packaging and regulatory guidelines to clients, involve experts as required.
• Keep abreast of current trends and literature, share with the team.
• Practice standard project reporting procedures to client and management (i.e. minutes, agendas, etc.)
• Works with management to resolve project issues and resources constraints within the team.
• Maintain positive team member interactions and manage conflict with assistance from Senior Manager Clinical Operations & Director, PDS Global Clinical Packaging Operations. 
• Make presentations and contribute to team meetings and occasionally to department meetings.
• Author, revise and train on Standard Operating Procedures (SOPs) relating to job responsibilities

Business Management:

• Plan, monitor and ensure completion of all activities outlined in the client quote for each project.  Prepare amendments for changes of scope in a timely manner.
• Create and maintain client timelines within Microsoft Project.   
• Contribute to Unit monthly forecasts by managing project Expected Monetary Values (EMVs).

SKILLS/EXPERIENCE REQUIRED:

• Minimum Bachelor of Science (B.Sc.) in Pharmacy or a related field
• Minimum 3 years experience in the pharmaceutical industry, with minimum 2 years pharmaceutical development experience
• Alternately, a Pharmacy Assistant Diploma with minimum 3 years experience in clinical packaging
• Well organized and detail oriented
• Strong interpersonal skills, as well as the ability to motivate. Client interface experience as asset.
• Proficiency with English language
• Proficiency using Microsoft Office applications
• Ability to meet deadlines and prioritize multiple tasks
• Excellent written and oral communication skills.
• Strong team skills
• Strong problem solving and evaluation skills
• Knowledge of Good Manufacturing Practices requirements in adherence to Therapeutic Products Programme (TPP), United States Food and Drug Administration (FDA) and Marketing Authorization Application (MAA) standards.
• Demonstrated commitment to our fundamental principles of Integrity, Respect & Excellence

HOW TO APPLY:

Qualified applicants are requested to apply by submitting their resume via email to bro.hr@patheon.com.  Please quote the job title and reference code in the subject line.

A criminal Record Search will be required of the identified candidate, to verify the absence of a criminal record for which a pardon has not been granted.

Patheon Inc. is an equal opportunity employer and is committed to the principle of diversity and is particularly interested in receiving applications from a broad spectrum of people.

DUTIES:        

• Testing of raw materials, packaging components, finished product, and stability samples while meeting deadlines and following assigned schedules.
• Accurate documentation of all tests, test materials, equipment used, and all results obtained.
• Work in a safe manner in accordance with approved methods, Standard Operating Procedures (SOP’s), Good Manufacturing Practices (GMP’s) / Good Laboratory Practices (GLP’s) while performing tests, and maintain a clean and organized work environment.
• Other related duties as assigned.

QUALIFICATIONS:

• Bachelor of Science (B.Sc.) degree or Community College Diploma in Chemistry, or in a related field. 
• Minimum 1-2 years of experience in the Pharmaceutical Industry.
• Must be a detail oriented individual with excellent organizational skills.
• Solid computer experience including lab software, Microsoft Word and Excel.
• Excellent verbal and written communication skills.
• Self-motivated individual with the ability to meet multiple deadlines.
• Theoretical and working knowledge of instrumentation such as High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Infrared (IR), Ultraviolet (UV), and analytical methods.
• Knowledge in GLP's and GMP's.
• Proficiency with the English language.
• Demonstrated commitment to our fundamental principles of Integrity, Respect and Excellence.