VP Client Management Jobs in Ontario

Minimum of 10 years' experience in Pharmaceutical QA management cross-functional teams, including QC operations.

Ensure accuracy and compliance of data and information provided to auditing/regulatory bodies, clients, management, and stakeholders.

Implement robust document management, data integrity and retention policies, Quality risks management and governance program, and quality review and escalation process.

Develop and implement regular facility lifecycle reviews against GMP requirements, including quality systems and tools.

Develop programs for supplier and vendor audit and qualification to meet AtomVie's quality and GMP standards.

Support regulatory team in completing, submitting, and responding to regulatory affairs requirements.

Proven track record driving growth with minimum 3-5 years of experience in management consulting or professional services

Develop and implement operational best practices across the entire organization with a focus on client experience

Work closely with all departments to jointly embed and facilitate client experience excellence ownership and alignment

Drive a ‘best in class’ experience for our clients measuring outcomes with KPI’s and other benchmarks

Create a consistent strategy to proactively manage client issues with a view to long-term engagement and retention

University graduate or equivalent with 12+ years related experience

Title: Risk Management Specialist (AVP/VP)

• Concentration Limit Management – Review, challenge and approve limit proposals

• Concentration Inventory Management – Review, Challenge, Approve and Maintain Concentration Inventory

• Identify, Measure, Monitor and Report Concentration Risk (Board SOR, ECRM Management report (monthly))

Hope you are doing well,

• Linkages of other areas such as Stress Testing (CCAR/Rapid Stress Testing), Top Risk/MRI, Risk Appetite

Title: Risk Management Specialist (SVP/VP)

Hope you are doing well,

• Decks for IA communication

• Organize and package artifacts for IA

• Write IA submission summaries

• Consent order and MRA submission materials