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Lead Executive - Site Support
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#661988
Full Time
Job Description
About Apotex Inc.
Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.
For more information visit: www.apotex.com .
Job Summary
Responsible for processing and managing changes required to Master Production and Packaging documentation; maintaining the Document management and SOD system for Apotex .
Job Responsibilities
Provide coaching, assistance and ongoing support to Change Owners on requirements for completing Change Control packages.
Responsible for creating and/or making formatting changes and edits to draft master documents.
Serve as a technical resource in the development of Master Production & Packaging documentation by advising on current Document Naming Conventions, Active Standard Instruction requirements & Master Template issues.
Conduct Detailed Impact Analysis for Master Production Documents according to proposed change details.
Perform functions related posting and publishing approved documents.
Responsible for initiating change control packages in the change management system with detailed change(s) descriptions and the corresponding rationale(s) for Manufacturing, Packaging, POMSNET recipes, SODs and supporting SAP information.
Review the accuracy of all manufacturing instructions imported into master documents during detailed Impact Analysis as listed in the scope of the change request.
Track and follow up the progress of change control requests to meet committed business timelines.
Using the LEAN tools and methodology, work as a change agent to drive and facilitate positive change - continuous improvement.
Lead, facilitate and/or support the development of project design, justification, and scope, in collaboration with process owners and other key stakeholders.
Develop and revise Standard Operating Documents governing and relating to Manufacturing Support functions as required.
Organize and implement all SOD change requests to defined deadlines.
Complete detailed impact analysis on SOD change requests.
Provide expertise to customers on the development of Site SODs.
Manage the document approval process using Content Server and QMS trackwise.
Demonstrate Behaviours that exhibit our organizational Values: Integrity, Teamwork, Courage, and Innovation.
Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
Job Requirements
Education
Bachelor’s/ Master’s degree in Science / Pharmacy
Knowledge, Skills and Abilities
Strong verbal and written English communication skills.
Excellent organization and writing skills
Understanding of GMPs, SODs.
Strong presentation skills to facilitate communication of initiatives in various forums - small group presentations, large employee meetings and briefings with senior leadership
Proven strong organizational, time management, and project management skills. Demonstrated experience in coordinating project activities
Strong knowledge of GMP
Proficiency with Word, Excel, Powerpoint, and Project Management .
Experience
Minimum of eight years relevant working experience in the pharmaceutical industry.
At Apotex, we are committed to fostering a welcoming andaccessible work environment, where all everyone feels valued, respected, and supported to succeed.
We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.
Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.
For more information visit: www.apotex.com .
Job Summary
Responsible for processing and managing changes required to Master Production and Packaging documentation; maintaining the Document management and SOD system for Apotex .
Job Responsibilities
Provide coaching, assistance and ongoing support to Change Owners on requirements for completing Change Control packages.
Responsible for creating and/or making formatting changes and edits to draft master documents.
Serve as a technical resource in the development of Master Production & Packaging documentation by advising on current Document Naming Conventions, Active Standard Instruction requirements & Master Template issues.
Conduct Detailed Impact Analysis for Master Production Documents according to proposed change details.
Perform functions related posting and publishing approved documents.
Responsible for initiating change control packages in the change management system with detailed change(s) descriptions and the corresponding rationale(s) for Manufacturing, Packaging, POMSNET recipes, SODs and supporting SAP information.
Review the accuracy of all manufacturing instructions imported into master documents during detailed Impact Analysis as listed in the scope of the change request.
Track and follow up the progress of change control requests to meet committed business timelines.
Using the LEAN tools and methodology, work as a change agent to drive and facilitate positive change - continuous improvement.
Lead, facilitate and/or support the development of project design, justification, and scope, in collaboration with process owners and other key stakeholders.
Develop and revise Standard Operating Documents governing and relating to Manufacturing Support functions as required.
Organize and implement all SOD change requests to defined deadlines.
Complete detailed impact analysis on SOD change requests.
Provide expertise to customers on the development of Site SODs.
Manage the document approval process using Content Server and QMS trackwise.
Demonstrate Behaviours that exhibit our organizational Values: Integrity, Teamwork, Courage, and Innovation.
Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
Job Requirements
Education
Bachelor’s/ Master’s degree in Science / Pharmacy
Knowledge, Skills and Abilities
Strong verbal and written English communication skills.
Excellent organization and writing skills
Understanding of GMPs, SODs.
Strong presentation skills to facilitate communication of initiatives in various forums - small group presentations, large employee meetings and briefings with senior leadership
Proven strong organizational, time management, and project management skills. Demonstrated experience in coordinating project activities
Strong knowledge of GMP
Proficiency with Word, Excel, Powerpoint, and Project Management .
Experience
Minimum of eight years relevant working experience in the pharmaceutical industry.
At Apotex, we are committed to fostering a welcoming andaccessible work environment, where all everyone feels valued, respected, and supported to succeed.
We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.
