Senior Officer Production Hilton Pharma Karachi. If you are a Pharm-D or B-Pharm professional looking to build a strong and stable career in sterile pharmaceutical manufacturing, this is your opportunity to join one of Pakistan’s most reputable pharmaceutical companies — Hilton Pharma.

With a strong commitment to quality, compliance, innovation, and patient safety, Hilton Pharma is hiring for the position of Officer/Senior Officer Production (Sterile) at its Karachi facility. This role offers the chance to work in a regulated sterile manufacturing environment while gaining hands-on exposure to international quality standards such as cGMP, QMS, and EHS.

If you have 2–3 years of pharmaceutical production experience, particularly in sterile operations, this opportunity could be your next big career move.

📌 Position Overview

Job Title: Officer / Senior Officer Production (Sterile)
Company: Hilton Pharma
Industry: Pharmaceutical Manufacturing
Location: Karachi, Pakistan
Experience Required: 2–3 Years
Qualification: B-Pharm / Pharm-D
Application Deadline: 8th March 2026

🏭 About Hilton Pharma

Hilton Pharma is a leading pharmaceutical company known for producing high-quality medicines that meet both local and international regulatory standards. With a strong presence in sterile and non-sterile manufacturing, the company emphasizes:

• Regulatory compliance

• Quality assurance

• Operational excellence

• Patient safety

• Continuous improvement culture

The company operates under the philosophy of “Hope. Health. Happiness.”, reflecting its commitment to improving healthcare outcomes.

🎯 Role Summary: Officer/Senior Officer Production (Sterile)

The Officer/Senior Officer Production (Sterile) will be responsible for supervising and managing sterile manufacturing and packing operations while ensuring strict adherence to cGMP, SOPs, EHS, and Quality Management System (QMS) standards.

This is a hands-on supervisory role that requires technical expertise, documentation accuracy, SAP reporting knowledge, and strong floor management capabilities.

🔬 Key Responsibilities

Below is a detailed breakdown of what you’ll be doing in this role:

1️⃣ Supervision of Sterile Manufacturing Operations

• Oversee daily production and packing activities in sterile areas.

• Ensure smooth production flow with minimal downtime.

• Coordinate with engineering, QA, and warehouse teams.

• Monitor manpower allocation and productivity.

2️⃣ Compliance with cGMP & Quality Standards

• Ensure strict adherence to:

  • cGMP guidelines

  • SOPs

  • EHS (Environmental Health & Safety) standards

  • QMS protocols

• Maintain contamination control and sterile area discipline.

• Ensure hygiene and gowning compliance on production floors.

3️⃣ BMR/BPR Documentation & SAP Reporting

• Monitor completion of:

  • BMR (Batch Manufacturing Records)

  • BPR (Batch Packing Records)

• Ensure accurate documentation and zero compliance gaps.

• Enter yield, rejection, and labor hour data in SAP.

• Maintain data integrity and traceability.

4️⃣ In-Process Checks & Line Clearance

• Ensure proper line clearance before batch initiation.

• Monitor in-process quality checks.

• Control losses and reduce rejection rates.

• Identify and troubleshoot deviations in real time.

5️⃣ Production Efficiency & Loss Control

• Minimize wastage during sterile production.

• Monitor yields and compare with standard targets.

• Improve operational efficiency.

• Participate in root cause analysis for deviations.

🎓 Educational Requirements

To qualify for this role, candidates must have:

• B-Pharm or Pharm-D

• Strong understanding of:

  • Pharmaceutical manufacturing

  • Sterile processing

  • Documentation standards

Candidates with additional certifications in GMP, production management, or quality compliance will have an advantage.

💼 Experience Requirements

The ideal candidate should have:

• 2–3 years of relevant pharmaceutical production experience

• Preferably hands-on exposure in:

  • Sterile manufacturing

  • Aseptic processing

  • Injectable production lines

• Experience handling:

  • BMR/BPR documentation

  • SAP reporting

  • cGMP audits

🧠 Required Skills & Competencies

✔ Technical Skills

• Strong knowledge of cGMP regulations

• Understanding of sterile area protocols

• Familiarity with production documentation systems

• SAP data entry and reporting

• Knowledge of yield calculations and rejection analysis

✔ Soft Skills

• Good supervisory and leadership abilities

• Strong coordination skills

• Attention to detail

• Problem-solving mindset

• Ability to manage pressure on production floors

✔ Compliance & Quality Focus

• Strong documentation accuracy

• Zero tolerance for non-compliance

• Commitment to quality and patient safety

🌟 Why This Role is a Smart Career Move

Here are 7 powerful reasons to apply:

1. Work in a sterile pharmaceutical environment – Gain specialized experience.

2. Exposure to international GMP standards – Enhance your compliance knowledge.

3. SAP reporting experience – Valuable ERP exposure.

4. Supervisory role early in career – Fast-track leadership growth.

5. Strong industry reputation – Boost your professional profile.

6. Regulatory learning opportunities – Prepare for audits and inspections.

7. Stable pharmaceutical sector – Long-term career security.

📈 Career Growth Opportunities

This role can lead to:

• Senior Production Officer

• Assistant Manager Production

• Manager Sterile Operations

• Quality Assurance roles

• Validation & Compliance positions

With experience in sterile manufacturing, your demand in the pharmaceutical industry significantly increases.

🏢 Work Environment

You will work in:

• Controlled sterile production areas

• Cross-functional team settings

• Fast-paced manufacturing operations

• Regulated GMP-compliant environment

The role requires:

• Shift supervision

• Active floor presence

• Coordination with QA and Engineering

• Real-time problem-solving

📝 How to Apply

Interested candidates should:

1. Prepare an updated CV highlighting:

   • Sterile production experience

   • cGMP exposure

   • SAP knowledge

   • Documentation handling

2. Apply using the attached QR code in the original job advertisement.

3. Submit your application before 8th March 2026.

Location: Karachi
Deadline: 8th March 2026

Early applications are encouraged as shortlisting may begin before the deadline.

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🔎 Who Should Apply?

This role is ideal for:

• Fresh professionals with 2–3 years experience in pharma

• Sterile manufacturing specialists

• Pharm-D graduates seeking production leadership roles

• Candidates looking for growth in regulated pharma environments

• Professionals seeking career advancement in Karachi

🏁 Final Thoughts

If you are passionate about pharmaceutical manufacturing, quality compliance, and sterile operations, this is a fantastic opportunity to grow your career with a respected industry leader.

The Officer/Senior Officer Production (Sterile) role at Hilton Pharma offers not just a job — but a structured career path in one of the most regulated and respected sectors of the pharmaceutical industry.

Don’t miss the deadline.

📅 Apply before 8th March 2026
📍 Location: Karachi

Take the next step toward a rewarding pharmaceutical career today.