Assistant Manager Validation Hilton Pharma Karachi. Are you an experienced pharmaceutical professional with strong expertise in process validation, equipment qualification, and regulatory compliance? Hilton Pharma, under its Hinucon division, is hiring an Assistant Manager Validation for its Karachi-based manufacturing facility.

If you have 6+ years of pharmaceutical industry experience, in-depth knowledge of cGMP, WHO, EU GMP, PIC/S, and ICH guidelines, and hands-on validation experience, this role offers a leadership opportunity to advance your career in pharmaceutical quality and compliance.

📅 Last Date to Apply: 8th March 2026
📍 Location: Karachi, Pakistan
📩 Application Method: Apply via QR code (as mentioned in the official advertisement)

📌 Position Overview

Job Title: Assistant Manager Validation
Company: Hilton Pharma
Department: Validation / Quality Assurance
Location: Karachi
Experience Required: 6+ Years
Qualification: B-Pharm / Pharm-D / MSc Chemistry
Industry: Pharmaceutical Manufacturing

🏢 About Hilton Pharma

Hilton Pharma is a leading pharmaceutical manufacturer in Pakistan, recognized for its commitment to producing high-quality medicines that meet global regulatory standards. The company’s philosophy—Hope. Health. Happiness.—reflects its dedication to improving patient lives through strict compliance, innovation, and operational excellence.

Hilton Pharma operates within internationally recognized quality frameworks, ensuring all manufacturing and validation processes align with global regulatory authorities.

Joining Hilton Pharma means:

• Working in a cGMP-compliant manufacturing environment

• Engaging with global pharmaceutical standards

• Contributing to high-impact healthcare solutions

• Growing within a structured and compliance-driven culture

🎯 Role Summary

The Assistant Manager Validation will lead and manage validation strategies for processes, equipment, and computerized systems to ensure compliance with local and international regulatory standards.

This role plays a critical part in maintaining:

• Process consistency

• Equipment reliability

• Product safety

• Audit readiness

• Regulatory compliance

You will work closely with Quality Assurance, Production, Engineering, and Regulatory Affairs teams to maintain plant-level validation excellence.

🔬 Key Responsibilities

Below is a detailed overview of the responsibilities associated with this role:

📋 1. Validation Strategy Development

• Develop and execute validation and qualification strategies.

• Ensure compliance with local and international cGMP requirements.

• Design master validation plans aligned with regulatory standards.

⚙ 2. Equipment & Process Validation

• Lead IQ (Installation Qualification) activities.

• Conduct OQ (Operational Qualification) testing.

• Execute PQ (Performance Qualification) protocols.

• Manage cleaning validation studies.

• Oversee hold time studies.

• Conduct Computer System Validation (CSV) activities.

📝 3. Documentation & Compliance

• Prepare validation protocols and reports.

• Review and approve validation documentation.

• Maintain comprehensive validation records.

• Ensure documentation meets WHO, EU GMP, PIC/S, and ICH standards.

🔎 4. Regulatory & Audit Support

• Support regulatory inspections and plant audits.

• Collaborate with cross-functional teams during inspections.

• Address audit observations and implement corrective actions.

• Ensure plant-level compliance during regulatory visits.

🤝 5. Cross-Functional Collaboration

• Coordinate with Engineering for equipment qualification.

• Work with Production teams for process validation.

• Partner with QA for compliance oversight.

• Assist Regulatory Affairs in documentation submission.

🎓 Educational Requirements

Candidates must possess one of the following qualifications:

• Bachelor of Pharmacy (B-Pharm)

• Doctor of Pharmacy (Pharm-D)

• MSc Chemistry

Additional certifications in GMP, validation, or quality management will be considered advantageous.

💼 Experience Requirements

Applicants must have:

• Minimum 6 years of pharmaceutical industry experience

• Proven experience in validation and qualification activities

• Strong understanding of manufacturing process controls

• Experience supporting regulatory inspections

Candidates with prior experience in sterile or non-sterile manufacturing facilities will have an added advantage.

🧠 Required Technical Expertise

To succeed in this role, you must demonstrate:

🔹 Validation Expertise

• Hands-on experience with IQ, OQ, PQ protocols

• Cleaning validation methodology

• Hold time study design and analysis

• Risk-based validation approach

🔹 Regulatory Knowledge

• WHO guidelines

• EU GMP requirements

• PIC/S compliance standards

• ICH validation guidelines

🔹 Analytical & Problem-Solving Skills

• Root cause analysis

• Risk assessment tools

• CAPA implementation

• Deviation handling

🔹 Documentation Mastery

• Technical writing skills

• SOP preparation

• Report review expertise

• Data integrity compliance

🌟 9 Powerful Reasons to Apply

1. Leadership-Level Role – Step into a managerial validation position.

2. Global Compliance Exposure – Work with WHO, EU GMP, PIC/S, and ICH standards.

3. Audit Readiness Experience – Participate in high-level regulatory inspections.

4. Technical Growth – Strengthen expertise in process and equipment validation.

5. Cross-Functional Collaboration – Engage with multiple plant departments.

6. Career Advancement – Clear path toward Validation Manager or QA leadership roles.

7. Reputable Employer – Join a recognized pharmaceutical manufacturer.

8. Structured Work Environment – Operate within international cGMP frameworks.

9. Meaningful Impact – Ensure product safety and regulatory compliance.

📍 Location: Karachi

This position is based in Karachi, Pakistan’s largest industrial and pharmaceutical hub. Working in Karachi provides:

• Exposure to leading pharmaceutical facilities

• Access to regulatory authorities

• Professional networking opportunities

• Career growth in a competitive pharma market

💰 Compensation & Benefits

Although specific salary details are not mentioned, Hilton Pharma typically offers:

• Market-competitive salary

• Professional development opportunities

• Structured corporate environment

• Exposure to international regulatory standards

Compensation will depend on:

• Experience level

• Technical expertise

• Validation portfolio

• Regulatory inspection exposure

👤 Ideal Candidate Profile

You are an ideal candidate if you:

✔ Have 6+ years of pharmaceutical validation experience
✔ Hold B-Pharm, Pharm-D, or MSc Chemistry qualification
✔ Possess hands-on IQ/OQ/PQ experience
✔ Understand global GMP frameworks
✔ Have strong documentation and analytical skills
✔ Can lead cross-functional validation initiatives
✔ Are confident during audits and inspections

📈 Career Growth Opportunities

This role can lead to:

• Validation Manager

• Senior QA Manager

• Head of Quality Systems

• Regulatory Compliance Lead

• Technical Operations Manager

Experience at Hilton Pharma significantly enhances your professional credibility in the pharmaceutical quality domain.

📝 How to Apply

Interested candidates must apply by sending their CV via the QR code provided in the official advertisement.

📅 Last Date: 8th March 2026

Application Tips:

• Highlight validation projects handled.

• Mention IQ/OQ/PQ experience clearly.

• Include regulatory inspection exposure.

• Quantify achievements (e.g., zero audit observations, successful inspections).

• Emphasize cleaning validation and CSV expertise.

🎤 Interview Preparation Guide

Prepare to discuss:

• Validation lifecycle approach

• Risk-based validation methodology

• Handling deviations and CAPA

• Regulatory inspection experiences

• Cleaning validation case studies

Demonstrate technical depth along with leadership capability.

🔒 Professional Expectations

As Assistant Manager Validation, you will be expected to:

• Maintain strict cGMP compliance

• Ensure documentation accuracy

• Lead validation initiatives confidently

• Support audits effectively

• Maintain high standards of data integrity

🎯 Final Thoughts

The Assistant Manager Validation position at Hilton Pharma is a prestigious opportunity for experienced pharmaceutical professionals seeking growth in validation leadership.

If you are passionate about quality systems, regulatory compliance, and process excellence, this role provides the ideal platform to strengthen your career while contributing to public health and patient safety.

🌿 Be part of an organization committed to Hope. Health. Happiness.

📩 Apply before 8th March 2026 and take the next step toward pharmaceutical leadership.