Are you a pharmaceutical professional with expertise in quality control, analytical testing, and stability studies? Are you looking for an opportunity to work with one of Pakistan’s leading pharmaceutical organizations? If yes, then Hilton Pharma is offering an excellent career opportunity for the position of Officer/Senior Officer QC (Stability) at its facility in Karachi.

This role is ideal for candidates who possess a strong academic background in pharmaceutical sciences or chemistry and have hands-on experience in quality control laboratories. The selected candidate will play a crucial role in stability testing, regulatory compliance, analytical evaluation, and maintaining product quality throughout the product lifecycle.

If you have experience working with analytical instruments such as HPLC, FTIR, and UV Spectrophotometers and are passionate about pharmaceutical quality assurance, this opportunity could be your next major career step.

About Hilton Pharma

Hilton Pharma is one of Pakistan’s leading pharmaceutical manufacturers, recognized for producing high-quality healthcare products that meet local and international quality standards.

The company has built a strong reputation for innovation, research, regulatory compliance, and commitment to patient safety. Through advanced manufacturing facilities and robust quality systems, Hilton Pharma continues to contribute significantly to Pakistan’s healthcare industry.

The organization’s philosophy of “Hope, Health, Happiness” reflects its commitment to improving lives through quality healthcare solutions.

Working at Hilton Pharma provides professionals with exposure to modern pharmaceutical technologies, international quality standards, and continuous learning opportunities.

Position Overview

Job Title

Officer / Senior Officer QC (Stability)

Department

Quality Control (QC)

Functional Area

Stability Studies and Analytical Testing

Location

Karachi, Pakistan

Industry

Pharmaceutical Manufacturing

Employment Type

Full-Time Permanent Position

Application Deadline

19 June 2026

What Is a QC Stability Officer?

A Quality Control Stability Officer is responsible for evaluating the stability of pharmaceutical products under different environmental conditions to ensure they remain safe, effective, and compliant throughout their shelf life.

Stability studies help determine:

• Product shelf life
• Storage requirements
• Packaging suitability
• Product degradation patterns
• Regulatory compliance

The role is essential because pharmaceutical companies must provide scientific evidence that their products maintain quality and effectiveness until the expiration date.

Educational Requirements

Candidates must possess one of the following qualifications:

Preferred Academic Qualifications

• MSc Chemistry
• Doctor of Pharmacy (Pharm D)

Candidates with strong academic performance and relevant laboratory exposure will be preferred.

Experience Requirements

Applicants should have:

Professional Experience

• 1 to 3 years of relevant experience in pharmaceutical quality control or stability testing.

Preferred Experience Areas

• Stability studies
• Quality control laboratories
• Pharmaceutical manufacturing
• Analytical testing
• Laboratory documentation
• Regulatory compliance

Candidates familiar with pharmaceutical testing environments and GMP-regulated laboratories will have a significant advantage.

Key Responsibilities

The selected candidate will be responsible for various stability testing and quality control activities.

1. Perform Chemical Analysis of Stability Samples

A major responsibility involves conducting chemical testing of pharmaceutical products undergoing stability studies.

This includes:

• Assay testing
• Impurity analysis
• Content uniformity evaluation
• Degradation product assessment
• Specification compliance verification

Accurate testing ensures products remain effective throughout their intended shelf life.

2. Conduct Physical Analysis of Stability Samples

Physical characteristics are equally important in determining product quality.

Responsibilities include evaluating:

• Appearance
• Color
• Odor
• Dissolution characteristics
• Moisture content
• Physical integrity

These assessments help identify changes that may occur during storage.

3. Maintain Stability Data and Records

Documentation is a critical aspect of pharmaceutical quality systems.

The QC Stability Officer will:

• Maintain testing records.
• Update stability protocols.
• Organize analytical reports.
• Ensure data traceability.
• Maintain audit-ready documentation.

Proper documentation supports regulatory inspections and quality assurance activities.

4. Manage Stability Testing Schedules

The selected candidate will ensure samples are tested according to approved timelines.

Responsibilities include:

• Scheduling stability testing activities.
• Monitoring due dates.
• Tracking sample status.
• Coordinating laboratory workflows.
• Ensuring timely completion of studies.

Effective scheduling helps prevent delays in product registration and compliance processes.

5. Monitor Climatic Chambers

Stability samples are stored under controlled environmental conditions.

The candidate will:

• Monitor chamber temperature.
• Verify humidity levels.
• Review environmental logs.
• Report deviations.
• Ensure proper chamber performance.

Accurate environmental control is essential for reliable stability results.

6. Manage Sample Placement and Withdrawal

The QC Stability Officer will oversee sample management throughout the stability study process.

Responsibilities include:

• Sample placement in chambers.
• Tracking storage conditions.
• Sample withdrawal at designated intervals.
• Maintaining sample accountability.
• Ensuring protocol compliance.

Proper sample handling ensures data accuracy and reliability.

7. Ensure SOP Compliance

The pharmaceutical industry operates under strict Standard Operating Procedures (SOPs).

The selected candidate must:

• Follow approved procedures.
• Ensure laboratory compliance.
• Maintain process consistency.
• Support internal audits.
• Participate in quality improvement initiatives.

Compliance minimizes risks and ensures reliable analytical results.

8. Support Regulatory Compliance

The role requires adherence to pharmaceutical regulations and global quality standards.

The candidate will work according to:

• ICH Guidelines
• WHO Guidelines
• BP (British Pharmacopoeia)
• USP (United States Pharmacopeia)
• EP (European Pharmacopoeia)

Compliance with these standards ensures product quality and regulatory acceptance.

Required Technical Knowledge

The ideal candidate should possess strong understanding of:

Pharmaceutical Guidelines

BP (British Pharmacopoeia)

Provides official quality standards for medicines and pharmaceutical ingredients.

USP (United States Pharmacopeia)

Defines analytical methods and acceptance criteria used globally.

EP (European Pharmacopoeia)

Establishes pharmaceutical quality standards for European markets.

ICH Guidelines

Provide internationally harmonized standards for pharmaceutical development and quality.

WHO Guidelines

Support global pharmaceutical quality assurance and compliance requirements.

Analytical Instrument Experience

Hands-on laboratory experience is essential.

Candidates should be familiar with:

HPLC (High Performance Liquid Chromatography)

Used for:

• Assay determination
• Impurity profiling
• Stability testing
• Quantitative analysis

FTIR (Fourier Transform Infrared Spectroscopy)

Used for:

• Raw material identification
• Functional group analysis
• Product verification

UV Spectrophotometer

Used for:

• Quantitative analysis
• Dissolution testing
• Concentration determination

pH Meter

Used for:

• Solution analysis
• Stability evaluation
• Product quality assessment

Experience with additional laboratory instruments will be considered advantageous.

Essential Skills Required

Successful candidates should possess:

Technical Skills

• Stability testing
• Pharmaceutical analysis
• Method execution
• Laboratory operations
• Regulatory compliance
• Data interpretation

Documentation Skills

• Report writing
• Data recording
• Laboratory documentation
• Record management

Analytical Skills

• Critical thinking
• Root cause analysis
• Data evaluation
• Problem-solving

Soft Skills

• Attention to detail
• Communication skills
• Time management
• Team collaboration
• Professional integrity

Career Growth Opportunities

This position provides an excellent pathway for advancement within the pharmaceutical industry.

Potential future roles include:

• Senior QC Officer
• QC Supervisor
• Stability Study Coordinator
• Quality Assurance Officer
• Laboratory Supervisor
• QC Manager
• Validation Specialist
• Regulatory Affairs Professional

The experience gained in pharmaceutical quality systems is highly valuable both locally and internationally.

Why Join Hilton Pharma?

Employees enjoy numerous professional advantages:

Industry Reputation

• Work with one of Pakistan’s leading pharmaceutical organizations.

Professional Development

• Exposure to international pharmaceutical standards.
• Continuous learning opportunities.

Advanced Laboratory Environment

• Work with modern analytical equipment.
• Gain hands-on experience in stability studies.

Career Advancement

• Opportunities for long-term professional growth.
• Structured quality and compliance environment.

Meaningful Contribution

• Help ensure the safety and effectiveness of pharmaceutical products used by patients.

Ideal Candidate Profile

The ideal applicant will be:

• Detail-oriented
• Analytical
• Quality-focused
• Organized
• Committed to compliance
• Technically competent
• Eager to learn and grow

Professionals who enjoy laboratory work, scientific analysis, and maintaining pharmaceutical quality standards will thrive in this role.

How to Apply

Interested candidates should submit their applications before the closing date.

Application Deadline

19 June 2026

Location

Karachi, Pakistan

Application Method

Apply through the QR code provided in the official job advertisement and submit your updated CV along with relevant educational and professional details.

Final Thoughts

The Officer/Senior Officer QC (Stability) position at Hilton Pharma presents an outstanding opportunity for pharmaceutical professionals seeking to build a rewarding career in quality control and stability testing. With responsibilities covering analytical testing, stability studies, documentation management, regulatory compliance, and laboratory operations, this role offers valuable exposure to critical pharmaceutical quality functions.

Candidates with an MSc in Chemistry or Pharm D qualification, relevant QC experience, and expertise in analytical instruments such as HPLC, FTIR, and UV Spectrophotometers are strongly encouraged to apply and become part of a company dedicated to delivering hope, health, and happiness through quality healthcare products.