Manager Quality Assurance

Who We Are

CCL Pharmaceuticals is a global life sciences company committed to improving access to trusted healthcare. With a presence in more than 20 countries and six decades of impact, we work to enable Healthy, Happy Lives through science-backed solutions.

Our portfolio spans diabetes, cardiovascular, neurology, psychiatry, urology, oncology, immunology, biosimilars, cough and cold, vitamins, minerals, and supplements segments, to name a few. Across all markets, over 3,000 people combine scientific expertise, local insight, and a shared purpose to enhance how individuals live, heal, and care for themselves.

Joining CCL Pharmaceuticals means stepping into a collaborative, mission-driven environment where your growth matters as much as your contribution. We enable you to learn, lead, and innovate through every stage of your journey, because the impact we make in healthcare begins with how you Grow with CCL.

What You'll Do

In this role, you will lead the planning, execution, and continuous improvement of qualification and validation activities across manufacturing, utilities, facilities, equipment, cleaning processes, analytical methods, and production processes in accordance with the Validation Master Plan (VMP) and global regulatory requirements. You will oversee the development and maintenance the Validation Master Plan, review validation protocols and reports, coordinate qualification activities with Engineering and Manufacturing teams, administer Product Quality Reviews (PQRs), support regulatory inspections and new product registrations, and drive continuous improvements that strengthen compliance, inspection readiness, and operational excellence.

You Are Good At

• Leading qualification and validation programs across manufacturing operations.
• Developing and executing Validation Master Plans (VMP).
• Reviewing validation protocols, reports, and technical documentation with accuracy and attention to detail.
• Managing cross-functional validation projects and balancing competing priorities.
• Administering Product Quality Reviews (PQRs) and driving timely follow-up actions.
• Interpreting GMP, PIC/S, and regulatory requirements to ensure compliant validation practices.
• Supporting regulatory inspections and validation documentation for product registrations.
• Building collaborative relationships across Manufacturing, Engineering, Quality Control, and Regulatory Affairs functions.
• Applying analytical thinking and structured problem-solving to quality and validation challenges.
• Driving continuous improvement across quality and validation systems.

What You'll Bring

• Pharm.D, or Master's in Chemistry from and HEC recognized university.
• 7-8 years of experience in Qualification, Validation, or Quality Assurance within a pharmaceutical manufacturing organization.
• Strong expertise in Validation Master Planning, Process Validation, Cleaning Validation, Analytical Method Validation, Equipment Qualification, Utility Qualification, and Facility Qualification.
• Sound knowledge of Product Quality Reviews (PQR), cGMP, PIC/S, and international regulatory requirements.
• Experience supporting regulatory inspections and validation documentation for new product registrations.
• Proficiency in Microsoft Office and documentation management systems.
• Strong analytical, leadership, presentation, communication, and stakeholder management skills.

Who You'll Work With

This role reports directly to the General Manager Quality Assurance and works closely with teams across Quality Assurance, Manufacturing, Engineering, Quality Control, Regulatory Affairs, Supply Chain, and other operational functions to strengthen validation excellence, regulatory compliance, and quality systems across the organization.

The culture you'll experience is shaped by three principles:

• Transparency in communication, goals, and decision-making.
• Inclusion in how people are developed, supported, and empowered.
• Performance-driven mindset that links quality excellence to business outcomes.

Our values guide how we work every day:

• Integrity First – Doing the right thing, consistently.
• Collaborate to Win – Building success together.
• Passion to Grow – Continuous learning and development.
• Innovation to Excel – Improving impact through better ideas.

What We Offer

Opportunity to lead qualification and validation initiatives within a globally growing pharmaceutical organization.

Exposure to international regulatory standards, validation practices, and quality systems.

Cross-functional leadership opportunities across Manufacturing, Engineering, Quality Control, and Regulatory Affairs.

A collaborative workplace focused on innovation, compliance, and continuous improvement.

Important Notice

CCL Pharmaceuticals is an equal opportunity employer. All applicants are considered based on merit, qualifications, and organizational need. We are committed to fostering an inclusive environment that respects diverse backgrounds, perspectives, and experiences.

For more information about this opportunity and to apply, please visit our website: Sign In - Applicant Portal