Formulation R&D Lead – End-to-End Pharma

CCL Pharmaceuticals

Lahore

On-site

PKR 1,200,000 - 2,400,000

Full time

3 days ago
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Benefits offered by this job

End-to-end formulation development
Scale-up exposure
Structured learning environment
Clear growth pathways

Job summary

CCL Pharmaceuticals in Sundar, Pakistan, invites applications for a Formulation R&D Specialist. You will develop and optimize pharmaceutical formulations from concept to commercialization, ensuring quality, regulatory compliance, and scalable manufacturing across in-house and third-party setups.

The role involves pilot trials, pre-formulation studies, scale-up support, technology transfer, and documentation.

Qualifications

  • Pharm-D or equivalent qualification from an HEC-recognized university.
  • 3–5 years of experience in formulation R&D in the pharmaceutical industry.
  • In-depth understanding of formulation development, scale-up, and transfer.
  • Strong analytical and problem-solving skills.
  • Effective communication and project coordination abilities.
  • Time management and documentation discipline.
  • Familiarity with lean practices and process improvement frameworks.

Responsibilities

  • Support development of pharmaceutical formulations from concept to commercialization.
  • Design and optimize stable, scalable formulations meeting quality and regulatory standards.
  • Support pilot trials, pre-formulation studies, scale-up, and troubleshooting.
  • Contribute to technology transfer and regulatory documentation.
  • Assist with supervisory duties to ensure continuity across R&D operations.

Skills

Formulation development
Stability testing
Technology transfer
Scale-up
Documentation
Pre-formulation
Regulatory awareness
Lean & process improvement
HSE awareness
Analytical skills

Education

Pharm-D or equivalent qualification from an HEC recognized university

Job description

CCL Pharmaceuticals in Sundar, Pakistan, invites applications for a Formulation R&D Specialist. You will develop and optimize pharmaceutical formulations from concept to commercialization, ensuring quality, regulatory compliance, and scalable manufacturing across in-house and third-party setups.

The role involves pilot trials, pre-formulation studies, scale-up support, technology transfer, and documentation.

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