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Adherence to all Good Manufacturing Practices (GMP) Safety Standards OfficeJob Description
Business Title: Project Leader I Quality
Effective Date: .2023
Revision #: 1
Version #: 2.0 CURRENT
Replaces: .2021
Summary:
Manage a portfolio of Clients and update quality plans/quality performance for clients supports product transfers from Pharmaceutical Development Services (PDS) and external to Commercial operations. Provide on floor Quality (Q) support attend RAPIDS and performs deviation investigations. Participate in Failure Mode and Effect Analysis (FMEAs) and process improvements determined from trending data.
Essential Functions:
Manage multiple smallmedium projects and/or improvement initiatives
Plan monitor and ensure completion of Metrics CAPAs and quality approvals
Manage client satisfaction by updating quality plans and coordinates customer requests
REQUIRED QUALIFICATIONS
Education:
College/Technical School Diploma in related field
Bachelor of Science (. in Chemistry Pharmacy Microbiology or Engineering an asset
Experience:
Minimum 5 years of previous related experience in pharmaceutical/food/cosmetic industry preferably in a QA function
Minimum 2 years pharmaceutical development experience
Project management experience or client management experience an asset
Equivalency:
Equivalent combinations of education training and relevant work experience may be considered.
Knowledge Skills and Abilities:
Strong selfmotived individual. Ability to work independently and within a team environment. Well organized and detail oriented with the ability to meet deadlines. Ability to prioritize multiple tasks. Strong interpersonal skills. Experience with Good Manufacturing Practices. Established quality regulatory and production mentality including an appreciation for client service and the contract manufacturing industry. Excellent written and oral communication skills. Proficiency using MS Office applications. Proficiency with English language.
Standards and Expectations:
Follow all Environmental Health & Safety Policies and Procedures. Work collaboratively with fellow team members modelling positive team principles and partnering to meet project and departmental objectives. Carry out all duties within strict compliance to Patheon quality systems Standard Operating Procedures (SOPs) and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Effectively engage in and adhere to departmental systems to maintain a smooth and efficient workflow (visual management scheduling systemsetc.. Be client and patient consciousat all times. Understand Key Performance Indicators and strive to improve the performance of the team by identifying areas for system improvements and engage in problem solving. Model positive thinking and is open to change motivating the team to adapt to shifts in priorities and new ways of working. Proactively identify areas for improvement in the of procedures. Communicate risks to timelines in a proactive manner. Consistently strives to improve skills and knowledge in related field.
Physical Requirements:
Light physical effort and fatigue. Walks sits or stands for limited periods. May require occasional equipment operation including keyboard equipment. Lifts light items for limited duration. Typically located in a comfortable indoor area. There may be exposure to mild physical discomfort from factors such as dust fumes or odours temperature extremes loud noise strong drafts or bright lights. Use of Personal Protective equipment may be required and may include any of the following: safety glasses safety shoes lab coat gloves hair net beard cover safety apron respirator occasionally.
Disclaimer:
This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as a comprehensive statement of work responsibilities or requirements. Managers and supervisors may assign other duties as needed.
Nothing contained herein should be construed to create an employment contract. Occasionally required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully align with all obligations imposed by the legislation of each country in which it operates including the implementation of the EU Equality Directive in relation to the recruitment and employment of its employees.
Required Experience:
Senior IC
Full-Time