Production Compliance Manager - Toronto, Canada - Sanofi US

Sanofi US

Verified Company

Toronto, Canada

3 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Reference No. R2672427

Position Title:
Production Compliance Manager

Department:
B100 Adsorptions

Location:
Sanofi Pasteur Limited, Toronto

Sanofi Pasteur:
The world's leading vaccine company
Sanofi Pasteur, the vaccines division of Sanofi, is the largest company in the world devoted entirely to human vaccines. Our driving goal is to protect people from infectious diseases by creating safe and effective vaccines.

Our company distributes more than 1 billion doses of vaccine each year, making it possible to vaccinate more than 500 million people across the globe.

Sanofi Pasteur offers the broadest range of vaccines in the world, providing protection against 20 bacterial and viral diseases.

Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.

Position Summary:

The Production Compliance Manager is a detail oriented and results driven individual with a strong understanding of biologics manufacturing, cGMPs, root cause analysis and possesses exceptional technical writing skills.

The incumbent is responsible for leading Deviation Investigations, ensuring Shop Floor compliance and execution of continuous improvement initiatives as a result of Deviation Investigations within the B100 Manufacturing department.

Key Responsibilities:

Responsible for all critical, major and minor deviations associated with the Platform:

Determine the scope of the investigation by collaborating with Quality Operations (QO), Manufacturing and Subject Matter Experts (SME) as appropriate in real time on the shop floor.
Lead and develop an investigation strategy in collaboration with Manufacturing, Quality Operations, and SMEs.
Perform Root Cause Analysis by conducting Shop Floor Production Walkthrough (GEMBA), select appropriate analytical tools, collect and analyze data to determine the true root cause.
Identify expertise required for the investigation (MTech, Technical Services, QC, QOVS, QOSA, etc.).
Identify, coordinate and manage contributions from other departments.
Participate in Autonomous Production Team (APT) support team meetings for planning and execution of investigations.
Review and provide guidance on reports prepared by technical staff.
Prepare manufacturing investigations to support other functional areas as requested.
Write and manage associated documentation, actions and timelines.
Responsible to ensure that investigation reports and/or manufacturing investigation reports are clear, concise and comprehensive.
Manage the deviation review process and ensure deviation investigations are closed according to targeted timelines.
Ensure actions are assigned to the appropriate individuals and completed to meet timelines.

Develop appropriate corrective and preventive actions:

In collaboration with platform management and other stakeholders, develop appropriate CAPAs with a clearly defined scope to address the root cause.
Initiate CAPAs in the Quality System as required.
Support manufacturing staff on updating GMP documents arising from CAPAs.
Review CAPAs associated with recurring issues and escalate any issues to Platform Leaders.
Work with Platform Leaders to identify and develop process improvements to remediate risks.

Develop Investigation cases to present at Governance boards:

Work with SMEs and appropriate QO experts; develop assessment of risk to product, process and other stages.
Utilize the Deviation Review Board Governance as required.
Prepare for Regulatory inspections by drafting investigation briefing packages / hot topics as applicable.
Present and defend investigations and provide support to the area manager for process / procedure topics during Regulatory inspections and other audits.

Responsible for Shop Floor Compliance within the Platform:

Lead and manage Data Integrity activities, initiatives and continuous improvements within the Platform in collaboration with APT Support teams and QOVS.
Perform Shop Floor Production Walkthroughs (GEMBA) to identify compliance gaps.
Track and develop action plan to address gaps, as required.

Continuous Improvement and GMP Documentation Review within the Platform:

Lead continuous improvement initiatives as outputs of investigations and provide compliance direction and monitoring as related to Shop Floor operations.
Participate in special projects for production process improvement projects to meet GMP requirements and address inspection observations.
Provides metrics and other reports as required.
Support GMP Documentation review (BPRs, logbo