Chemical Engineer

Carryfor Pharmaceutical Pvt. Ltd.

Karachi Division

On-site

PKR 2,400,000 - 3,200,000

Full time

14 days+
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Benefits offered by this job

Communication
Gratuity
Incentive Bonus
Leaves
Medical
Provident Fund
Transport

Job summary

Carryfor Pharmaceutical PVT LTD in Karachi, Pakistan, is seeking a Chemical Process Engineer to lead process development, scale-up and production for pharmaceutical intermediates and APIs. You will report to the Process Development Lead and collaborate with production, QA and R&D to ensure GMP-compliant manufacturing.

The role emphasizes developing synthesis routes, preparing PFDs, mass and energy balances, and safe operations with a strong focus on process safety and continuous improvement.

Qualifications

  • Degree in Chemical Engineering or related discipline with strong fundamentals in reaction engineering and unit operations.
  • Experience with process development, scale-up and pilot plant operations in pharmaceutical or fine chemical manufacturing.
  • Knowledge of GMP, process safety (HAZOP, HIRA) and chemical hazard control measures.
  • Practical skills preparing mass/energy balances, PFDs, material specifications and SOPs.
  • Familiarity with analytical techniques for impurity control and collaboration with QC labs.
  • Experience using process simulation or calculation tools (ASPEN, MATLAB, Excel).
  • Strong documentation and change-control practices for regulated manufacturing.
  • Master’s degree or professional training in pharmaceutical process development.

Responsibilities

  • Develop, optimize and scale chemical synthesis routes and unit operations for API and intermediate production.
  • Prepare and review process flow diagrams (PFDs), mass and energy balances, and SOPs.
  • Perform process hazard analyses and risk assessments (HAZOP, HIRA) and implement safety controls.
  • Support troubleshooting of process deviations, yield losses and impurity issues with QA and analytical teams.
  • Work on equipment selection, pilot trials, and technology transfer from R&D to manufacturing.
  • Monitor process performance and lead continuous improvement activities.

Skills

Reaction engineering
Unit operations
GMP knowledge
HAZOP/HIRA
PFDs
Mass balances
Energy balances
SOPs
Impurity control
Documentation
Change control
Analytical techniques

Education

Chemical Engineering degree
Master’s degree in pharmaceutical process development

Tools

ASPEN
MATLAB
Excel

Job description

Job Description

Company: Carryfor Pharmaceutical PVT LTD

Location: Karachi, Pakistan (on-site)

Employment Type: Full-Time

Shift: On rotation

Role Summary
  • Work in process development, scale‑up and production for pharmaceutical intermediates and APIs.
  • Report to Process Development Lead and collaborate with production, QA and R&D to ensure safe, efficient, GMP‑compliant chemical manufacturing processes.
Key Responsibilities
  • Develop, optimize and scale chemical synthesis routes and unit operations for API and intermediate production.
  • Prepare and review process flow diagrams (PFDs), mass and energy balances, and SOPs.
  • Perform process hazard analyses and risk assessments (e.g., HAZOP, HIRA) and implement safety controls.
  • Support troubleshooting of process deviations, yield losses and impurity issues with QA and analytical teams.
  • Work on equipment selection, pilot trials, and technology transfer from R&D to manufacturing.
  • Monitor process performance and lead continuous improvement activities.
Job Specification
Must‑have
  • Degree in Chemical Engineering or related discipline with strong fundamentals in reaction engineering and unit operations.
  • Experience with process development, scale‑up and pilot plant operations in pharmaceutical or fine chemical manufacturing.
  • Knowledge of GMP, process safety (HAZOP, HIRA) and chemical hazard control measures.
  • Practical skills preparing mass/energy balances, PFDs, material specifications and SOPs.
  • Familiarity with analytical techniques for impurity control and collaboration with QC labs.
  • Experience using process simulation or calculation tools (e.g., ASPEN, MATLAB, Excel).
  • Strong documentation and change‑control practices for regulated manufacturing.
Preferred
  • Master’s degree or professional training in pharmaceutical process development.
Job Rewards and Benefits
  • Communication
  • Gratuity
  • Incentive Bonus
  • Leaves
  • Medical
  • Provident Fund
  • Transport
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