Sterile Production, Validation & QC Careers — Karachi

Hilton Pharma Limited, one of Pakistan’s leading pharmaceutical companies, is expanding its team and looking for qualified, experienced, and dedicated professionals to join our operations in Karachi. We are currently hiring for critical roles in Sterile Production, Validation, and Quality Control (Stability). If you are passionate about pharmaceutical excellence, quality compliance, and patient care, we encourage you to apply.

Location:

Karachi | Last Date to Apply: 8th March 2026

• Supervise manufacturing and packing operations in sterile production.
• Ensure compliance with SOPs, cGMP, EHS & QMS guidelines on the production floor.
• Monitor completion of BMR/BPR and ensure accurate SAP entries of yield and labor hours.
• Maintain line clearance, in-process checks, and control losses/rejections.

• Education:
  
  B. Pharm / Pharm
  
  D.
• Experience:
  
  2–3 years of relevant experience in pharmaceutical production (preferably sterile operations).
• Strong knowledge of cGMP and production documentation (BMR/BPR).
• Good supervision, coordination, and SAP reporting skills.
• Ability to manage floor operations and ensure compliance with quality standards.

Location:

Karachi | Last Date to Apply: 8th March 2026

• Develop and execute validation and qualification strategies in compliance with local and international CGMP requirements.
• Lead equipment and process validations (IQ, OQ, PQ), cleaning validation, hold time studies, and CSV activities.
• Prepare and review validation protocols, reports, and master validation plans.
• Support regulatory inspections, audits, and cross‑functional validation initiatives at plant level.

• Education:
  
  B.Pharm / Pharm-D or MSc Chemistry.
• Experience:
  
  6+ years of pharmaceutical industry experience.
• Strong hands‑on expertise in validation and qualification of processes and equipment.
• Sound knowledge of WHO, EU GMP, PIC/S, and ICH regulatory guidelines.
• Excellent analytical, documentation, and problem‑solving skills.

Location:

Karachi | Last Date to Apply: 8th March 2026

• Perform chemical and physical analysis of stability samples as per approved specifications.
• Maintain stability data, reports, and testing schedules in compliance with GLP & GDP.
• Monitor climatic chambers and manage sample placement and withdrawal.
• Ensure compliance with SOPs and pharmaceutical regulatory guidelines.

• Education:
  
  MSc (Chemistry) or Pharm
  
  D.
• Experience:
  
  1–3 years of relevant experience in pharmaceutical quality control/stability.
• Sound knowledge of pharmaceutical guidelines (BP, USP, EP, ICH & WHO).
• Hands‑on experience with HPLC, FTIR, UV Spectrophotometer, pH meter, and other analytical instruments.
• Strong documentation and analytical skills.

• Be part of a leading pharmaceutical company committed to quality healthcare.
• Work in a state‑of‑the‑art manufacturing facility with professional growth opportunities.
• Collaborate with experienced teams dedicated to excellence and compliance.
• Opportunity to contribute to meaningful work that impacts patient lives.
• Competitive compensation and career development prospects.
• Inclusive and supportive workplace culture.

• Applications must be submitted by March 8, 2026.
• Only shortlisted candidates will be contacted.
• Position is based in Karachi.