Senior Manager Engineering

CCL Pharmaceuticals; Lahore; Presencial; PKR 2.400.000 - 4.800.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Learning and development opportunities

Lead critical engineering operations

Exposure to regulatory compliance

Collaborative environment

Growth within a global pharma

Descripción de la vacante

CCL Pharmaceuticals is seeking a senior engineering leader for its Sundar site in Pakistan. You will oversee engineering, utilities, and facility operations to guarantee GMP-compliant infrastructure that supports uninterrupted production and product quality.

You will drive preventive maintenance, qualification, validation, and change control while managing budgets and technical resources. Collaboration with Production, Quality, HSE, and partners is essential to drive continuous improvement.

Formación

• BSc in Engineering; MS or equivalent qualification preferred by a HE C-recognized institute.
• 6–8 years of relevant pharmaceutical engineering experience.
• Strong knowledge of cGMP, EU GMP, GEP, qualification, validation, and change control.
• Experience with preventive maintenance, utilities management, and facility operations in regulated manufacturing.
• Proven track record leading projects, managing budgets, contractors, and technical teams.
• Lean manufacturing, process improvement, and risk-based root-cause analysis familiarity.
• Regulatory audits experience and engineering documentation skills.

Responsabilidades

• Lead engineering, utilities, and facility operations at Sundar site to ensure GMP-compliant infrastructure.
• Oversee preventive maintenance, qualification, validation, and change control.
• Manage budgets, resources, and engineering projects; drive continuous improvement.
• Collaborate with cross-functional stakeholders to resolve challenges and align priorities.
• Ensure safety, quality, and regulatory compliance across engineering operations.

Conocimientos

Team leadership

Engineering operations

Risk-based decision-making

Project management

Root-cause analysis

Safety & compliance

Contractor management

Cross-functional collaboration

Technical capability development

Educación

BSc in Engineering

MS or equivalent

Descripción del empleo

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 lead engineering, utilities, and facility operations at our Sundar manufacturing site in Pakistan, ensuring 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 while ensuring compliance with EU GMP and cGMP requirements. You will also lead engineering projects, manage budgets and technical resources, strengthen team capabilities, and drive risk-based problem-solving and continuous improvement to enhance operational efficiency, safety, and manufacturing performance.

You Are Good At

• Leading multidisciplinary engineering teams and building a culture of accountability and continuous improvement
• Ensuring equipment, utilities, and facility reliability to support consistent manufacturing performance
• Applying sound technical judgement and risk-based decision-making to complex engineering challenges
• Planning and executing engineering projects while managing budgets, timelines, and resources
• Driving structured root-cause analysis and sustainable improvements in operational performance
• Maintaining high standards of safety, quality, and compliance across engineering operations
• Managing contractors and technical partners to deliver operational and project objectives
• Collaborating effectively with cross-functional stakeholders to resolve challenges and align priorities
• Developing technical capabilities and strengthening team performance

What You'll Bring

• BSc 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.
• Demonstrated experience managing engineering projects, budgets, contractors, and technical teams.
• Working knowledge of lean manufacturing, process improvement methodologies, and risk-based root-cause analysis.
• Familiarity with engineering documentation, technical training, and regulatory audit requirements.

Who You'll Work With

This role reports to the Associate Director Engineering and works closely with Production, Quality, HSE, contractors, site leadership, and other cross-functional stakeholders to ensure reliable manufacturing operations, regulatory compliance, and effective delivery of engineering priorities.

Across functions and departments, you will collaborate with engineering teams, production personnel, quality professionals, and external partners to maintain operational reliability, uphold regulatory standards, and drive continuous improvement across manufacturing operations.

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.
• The opportunity to lead critical engineering, utilities, and facility operations that support quality pharmaceutical manufacturing.
• Exposure to strategic engineering projects, regulatory compliance, and operational improvement initiatives.
• A collaborative environment that values leadership, accountability, and continuous improvement.
• Opportunity to grow within a global pharmaceutical organization.

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.