Senior Manager Engineering

CCL Pharmaceuticals is a global life sciences company with over six decades of experience and operations in more than 20 countries. We are dedicated to expanding access to trusted healthcare by delivering high-quality, science-backed solutions across various therapeutic areas including diabetes, cardiovascular, neurology, psychiatry, urology, oncology, immunology, biosimilars, antibiotics, and supplements. Our team of over 3,000 professionals combines scientific expertise and local insight to improve how individuals live, heal, and care for themselves. Joining CCL means becoming part of a collaborative, mission-driven environment where your growth is valued alongside your contributions, enabling you to learn, lead, and innovate throughout your career.

Key Responsibilities
In this role, you will lead engineering, utilities, and facility operations at our Sundar manufacturing site in Pakistan. Your primary focus will be to ensure a safe, reliable, and GMP-compliant infrastructure that supports uninterrupted production and consistent product quality. You will oversee preventive maintenance, equipment and utility qualification, validation, and change control processes, ensuring compliance with EU GMP and cGMP standards. Additionally, you will manage engineering projects, budgets, and technical resources while strengthening team capabilities. Driving risk-based problem-solving and continuous improvement initiatives will be essential to enhance operational efficiency, safety, and manufacturing performance. You will also manage contractors and technical partners, collaborate with cross-functional teams, and maintain high standards of safety, quality, and compliance throughout engineering operations.

Required Qualifications
- Bachelor’s degree in Engineering, MS, or an equivalent qualification from an HEC-recognized institute.
- 6-8 years of relevant engineering experience, preferably within pharmaceutical manufacturing.
- Strong knowledge of cGMP, EU GMP, Good Engineering Practices (GEP), equipment and utility qualification, validation, and change control.
- Experience in preventive maintenance systems, utilities management, and facility operations within a regulated manufacturing environment.
- Proven ability to manage engineering projects, budgets, contractors, and technical teams effectively.
- Working knowledge of lean manufacturing principles, process improvement methodologies, and risk-based root-cause analysis.
- Familiarity with engineering documentation, technical training, and regulatory audit requirements.

Preferred Qualifications and Benefits
This position reports to the Associate Director of Engineering and involves close collaboration with Production, Quality, HSE, contractors, site leadership, and other stakeholders to ensure reliable manufacturing operations and regulatory compliance. The role offers exposure to strategic engineering projects, regulatory compliance efforts, and operational improvement initiatives within a global pharmaceutical organization.

At CCL Pharmaceuticals, the workplace culture is built on transparency, inclusion, and a performance-driven mindset. We value integrity, collaboration, passion for growth, and innovation, creating an environment where new ideas are welcomed and scaled for meaningful progress.

We provide learning and development opportunities to support continuous growth and leadership development. This role offers the chance to lead critical engineering, utilities, and facility operations that underpin quality pharmaceutical manufacturing. You will be part of a collaborative environment that values accountability and continuous improvement, with ample opportunity to grow within a global organization.

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