CCL Pharmaceuticals is a global life sciences company dedicated to improving access to trusted healthcare. With operations in over 20 countries and more than six decades of experience, we focus on enabling healthy, happy lives through science-backed solutions. Our diverse portfolio includes diabetes, cardiovascular, neurology, psychiatry, urology, oncology, immunology, biosimilars, cough and cold remedies, vitamins, minerals, and supplements. Over 3,000 professionals worldwide combine scientific expertise and local insights to enhance how individuals live, heal, and care for themselves. Joining CCL means becoming part of a collaborative, mission-driven environment where personal growth is valued alongside your contributions. We support learning, leadership, and innovation at every stage of your career because the impact we make in healthcare begins with how you grow with us.

Key Responsibilities
You will support the development of pharmaceutical formulations from concept through to commercialization. This includes designing and optimizing stable, scalable formulations that comply with quality, regulatory, and manufacturing standards, both in-house and with third-party partners. Your role will involve conducting pilot trials, pre-formulation studies, scale-up support, and troubleshooting formulation challenges. You will contribute to technology transfer activities, prepare regulatory documentation, and drive continuous improvement of existing formulations. Additionally, you may take on supervisory duties to maintain operational continuity and efficiency within R&D.

Required Qualifications
Candidates should hold a Pharm-D or an equivalent qualification from an HEC-recognized university. A minimum of 3 to 5 years’ experience in formulation research and development within the pharmaceutical industry is essential. A strong understanding of formulation development, scale-up processes, and technology transfer is required. Candidates must demonstrate excellent analytical and problem-solving skills, along with effective communication and project coordination abilities. Time management and disciplined documentation practices are critical. Familiarity with lean methodologies and process improvement frameworks is highly desirable. Proficiency in MS Office and internet-based research tools is expected.

Preferred Qualifications and Benefits
This position is plant-based at Sundar and reports directly to the Senior Executive Manager of Research & Development. You will collaborate closely with cross-functional teams including Manufacturing, Quality Assurance, Quality Control, Regulatory Affairs, and Engineering to ensure smooth product development and transfer. The company culture emphasizes transparency in communication and decision-making, inclusion in employee development and empowerment, and a performance-driven mindset that aligns capability building with business outcomes. Our core values are Integrity First, Collaborate to Win, Passion to Grow, and Innovation to Excel.

We offer the opportunity to work on end-to-end formulation development projects, gaining exposure to scale-up, technology transfer, and cross-functional plant operations. You will benefit from a structured learning environment within a growing global pharmaceutical organization, with hands-on experience interfacing with regulatory, quality, and manufacturing teams. The culture supports clear growth and progression pathways aligned with performance.

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

Job Details

Total Positions:
1 Post
Job Shift:
First Shift (Day)
Job Type:
Job Location:
Gender:
No Preference
Age:
18 - 65 Years
Minimum Education:
Bachelors
Degree Title:
bachelor degree
Career Level:
Mid-Level
Maximum Experience:
2 Years
Apply Before:
Nov 05, 2026
Posting Date:
Oct 30, 2026

CCL Pharmaceuticals

· 11-50 employees - Lahore

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