Assistant Manager Quality Control

Who We Are

CCL Pharmaceuticals is a global life sciences company working to expand access to trusted healthcare. With a presence in more than 20 countries and a legacy of six decades, we are committed to enabling Healthy, Happy Lives through high-quality, science-backed solutions.

Our portfolio spans diabetes, cardiovascular, neurology, psychiatry, urology, oncology, immunology and biosimilars, antibiotics, cough and cold, vitamins, minerals and supplements segments. Across all our markets, over 3,000 people bring together scientific expertise, local insight, and a shared sense of purpose to improve 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 play a critical role in ensuring the effective implementation of ISO/IEC 17025 standards and GMP compliance within the QC lab, focusing primarily on raw and packaging materials. You will oversee sampling, testing, documentation, and timely release of materials in accordance with approved specifications and regulatory expectations.

Your scope will also include managing laboratory documentation, participating in audits and proficiency testing, supporting regulatory submissions, and leading continuous improvement initiatives. The role involves close collaboration with Quality Assurance, Research & Development, and Regulatory Affairs to uphold CCL Pharmaceuticals’ standards of quality, data integrity, and laboratory excellence.

What You Are Good At

• Executing and validating raw and packaging material tests in compliance with GMP and ISO/IEC 17025
• Managing reference samples, test records, and laboratory documentation with precision and accuracy
• Reviewing and releasing analytical reports in line with internal quality plans and regulatory standards
• Identifying non-conformances and leading effective CAPA (Corrective & Preventive Actions)
• Supporting new product launches through method verification and validation
• Participating in audits, external proficiency testing, and laboratory performance improvement initiatives
• Collaborating with QA, RA, and R&D teams to ensure alignment and compliance

What You’ll Bring

• M.Sc. in Chemistry or a Pharmacy degree from an HEC-recognized institution
• Minimum 6 years of experience of raw material testing within the pharmaceutical industry
• Strong knowledge of GMP requirements and ISO/IEC 17025, and analytical testing standards
• Hands-on experience with laboratory equipment and analytical techniques (e.g., HPLC, UV, FTIR)
• Strong documentation, data integrity, and quality mindset
• Effective communication, time management, and cross-functional collaboration skills
• Proficiency in MS Office, and digital documentation systems

Who You’ll Work With

CCL Pharmaceuticals teams are united by a shared belief that great work happens when people feel valued, empowered, and supported. You will work with individuals who ask the right questions, push for better outcomes, and lead with integrity.

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

• Transparency in communication, goals, and decision-making
• Inclusion in how people are hired, developed, and heard
• Performance-driven mindset that connects individual contribution to shared success

This is a place where values are practiced every day:

• Integrity First – Trust is built through fairness, consistency, and doing what is right
• Collaborate to Win – Success is shared, and solutions are built together
• Passion to Grow – Learning is continuous, and ambition is supported with opportunity
• Innovation to Excel – New ideas are welcomed, tested, and scaled to drive meaningful progress

What We Offer

• Learning and development opportunities for continuous growth
• Exposure to regional and global projects with meaningful impact
• A workplace that values wellbeing, inclusion, and purposeful performance
• Opportunity to contribute to high-impact quality, compliance, and laboratory excellence initiatives

Important Notice

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