Manager, CMO Quality

CSL; Argentina; On-site; ARS 137,543,000 - 213,956,000; Full time

Benefits offered by this job

Global travel

Competitive benefits

Job summary

CSL Seqirus in Argentina seeks a Manager, CMO Quality to oversee external manufacturing partners, ensuring GMP compliance, quality systems alignment with CSL Seqirus standards, and regulatory readiness across key markets.

You will lead CMO quality oversight for API, Fill/Finish and Packaging, draft and maintain Quality Agreements, manage CAPA and change control, and coordinate with global MAH stakeholders; expect ~25% travel to sites.

Qualifications

• Minimum 5 years in a GxP environment.
• Knowledge of FDA, EU GMP, PIC/S, TGA and Health Canada.
• Experience with CMOs / third-party quality management.
• Ability to work in a global matrix organization.

Responsibilities

• CMO Relationship & Quality Oversight: primary regional quality interface for CMOs.
• Quality Agreements & Governance: draft, negotiate and maintain CMO Quality Agreements.
• Deviation, CAPA & Change Management: review and approve deviations and CAPAs; manage changes.
• Performance Monitoring & Escalation: track KPIs; escalate critical quality issues.

Skills

Quality oversight

GxP experience

Regulatory knowledge

CMO management

Cross-functional leadership

Quality systems

Communication skills

Bilingual English/Spanish

Education

Bachelor's in Life Sciences

Job description

About CSL Seqirus

CSL Seqirus is one of the world’s largest influenza vaccine companies and a global leader in pandemic preparedness. As part of the CSL Group, we operate at the intersection of cutting-edge science and meaningful human impact — protecting millions of lives every year. When you join CSL Seqirus, you join a team where quality is not a department, it’s a commitment.

The Opportunity:

Reporting to the Global Head of External Quality, the Manager, CMO Quality plays a critical role in ensuring the integrity, compliance, and continuity of our external manufacturing network. You will be the primary quality partner for assigned Contract Manufacturing Organizations (CMOs) — overseeing outsourced production activities including API, Fill/Finish, and Packaging — and serve as the trusted bridge between CSL Seqirus and our global CMO partners.

This is a high-visibility, globally connected role where your decisions directly protect product supply, patient safety, and regulatory standing across multiple markets.

What You’ll Do

CMO Relationship & Quality Oversight

• Serve as the primary regional quality interface for assigned CMOs, fostering strong, trust-based partnerships
• Ensure CMO quality systems are aligned with CSL Seqirus standards and applicable regulatory requirements
• Represent CSL Seqirus Quality in Joint Operational Meetings, Business Reviews, and on-site CMO visits

Quality Agreements & Governance

• Draft, negotiate, and maintain CMO Quality Agreements in compliance with FDA, EMA, PIC/S, TGA, and Health Canada regulations
• Oversee day-to-day execution of Quality Agreement commitments including training, recalls, and complaint management

Deviation, CAPA & Change Management

• Review, assess, challenge, and approve CMO deviations and CAPAs to ensure product quality and compliance
• Manage CMO-initiated changes and proactively communicate relevant updates to MAH stakeholders
• Review and approve GMP-controlled documents including SOPs, specifications, and validation reports

Performance Monitoring & Escalation

• Track and report CMO quality performance through globally aligned KPIs
• Identify quality trends and ensure timely corrective actions are implemented
• Escalate critical quality issues to senior stakeholders and drive resolution

Standardization & Continuous Improvement

• Drive harmonization of quality processes across the CMO network (change management, batch record review, complaints, recalls)
• Enhance CMO Quality Maturity and execute Quality Road Maps

Regulatory & Inspection Support

• Support regulatory inspections and audits at CMO sites as needed
• Assess and communicate potential regulatory impacts on CSL Seqirus business

Commercial Readiness & Growth

• Support Tech Transfer, product launches, and regulatory submissions for new CMO projects
• Act as Quality SME in cross-functional commercial readiness teams

What You’ll Bring

Education

• Bachelor’s degree (or higher) in Pharmacy, Chemistry, Biology, Biochemistry, or a related scientific discipline

Experience

• Minimum 5 years of experience in a GxP environment within the pharmaceutical, biotech, or regulated industry
• Demonstrated knowledge of FDA, PIC/S, EU GMP, TGA, and Health Canada regulatory frameworks
• Prior experience in CMO / third-party quality management highly preferred
• Proven ability to work effectively in a global matrix organization

Skills & Competencies

• Strong quality system knowledge — internal and external manufacturing environments
• Excellent organizational skills with the ability to manage multiple priorities across time zones
• High cross-cultural sensitivity and interpersonal effectiveness
• Managerial courage — able to hold compliance positions under pressure
• Strategic mindset with strong decision-making and risk assessment capabilities
• Outstanding written and verbal communication skills
• Fluency in English and Spanish is required (written and spoken)

What We Offer

• A globally connected role with real impact on product supply and patient safety
• Collaboration with world-class quality professionals across Americas, EMEA, and APAC
• A culture that values integrity, courage, and continuous improvement
• Competitive compensation and benefits aligned with multinational pharma standards
• Approximately 25% travel to CMO sites and CSL Seqirus locations

Our Commitment

CSL Seqirus is committed to building a diverse, equitable, and inclusive workplace. We welcome applicants from all backgrounds and are proud to be an equal opportunity employer.

Our Benefits

We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.

About CSL

CSL is a leading global biotechnology company with a dynamic portfolio of life‑saving medicines, including those that treat haemophilia and immune deficiencies, as well as vaccines to prevent influenza. Since our start in 1916, we have been driven by our promise to save lives through innovation. Learn more about CSL.