Website Hilton Pharma
Senior Officer QC Hilton Pharma Karachi. Are you a qualified Chemist or Pharm D professional looking to grow your career in pharmaceutical quality control? Hereβs your chance to join one of Pakistanβs leading pharmaceutical manufacturers, Hilton Pharma, under its Hinucon division.
The company is hiring an Officer / Senior Officer QC (Stability) for its Karachi-based facility. If you have hands-on experience in stability testing, strong analytical skills, and knowledge of international pharmaceutical guidelines, this opportunity could be your gateway to long-term professional success.
π Last Date to Apply: 8th March 2026
π Location: Karachi, Pakistan
π Position Overview
Job Title: Officer / Senior Officer QC (Stability)
Company: Hilton Pharma
Department: Quality Control β Stability
Location: Karachi
Qualification Required: MSc (Chemistry) or Pharm D
Experience Required: 1β3 years
Industry: Pharmaceutical Manufacturing
Application Method: Apply via QR code (as per official advertisement)
Application Deadline: 8th March 2026
π’ About Hilton Pharma
Hilton Pharma is a well-established pharmaceutical company in Pakistan, known for manufacturing high-quality medicines that comply with international standards. The organization is committed to delivering products aligned with global regulatory requirements and maintaining strict quality assurance protocols.
With a strong reputation for Hope, Health & Happiness, Hilton Pharma emphasizes:
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Innovation in pharmaceutical manufacturing
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Compliance with international quality standards
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Continuous professional development
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Ethical and responsible production
Working here means becoming part of a professional team dedicated to safeguarding public health through rigorous quality control systems.
π― Role Summary
The Officer / Senior Officer QC (Stability) will be responsible for conducting stability testing of pharmaceutical products, ensuring compliance with regulatory guidelines, and maintaining detailed documentation as per Good Laboratory Practices (GLP) and Good Distribution Practices (GDP).
This role is ideal for professionals who:
β Have hands-on experience in analytical testing
β Understand pharmaceutical regulatory frameworks
β Possess strong documentation skills
β Are detail-oriented and compliance-focused
π¬ Key Responsibilities
Below is a comprehensive overview of the job responsibilities:
π§ͺ 1. Stability Testing & Analysis
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Perform chemical and physical analysis of stability samples according to approved specifications.
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Conduct testing for finished products and raw materials.
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Ensure accurate and reproducible results.
π 2. Stability Data Management
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Maintain stability data records.
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Prepare detailed testing reports.
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Monitor testing schedules and ensure timely analysis.
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Maintain compliance with GLP & GDP standards.
π‘ 3. Climatic Chamber Monitoring
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Monitor temperature and humidity conditions in climatic chambers.
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Manage sample placement and withdrawal schedules.
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Ensure environmental conditions meet ICH stability guidelines.
π 4. SOP & Regulatory Compliance
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Ensure adherence to Standard Operating Procedures (SOPs).
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Maintain compliance with pharmaceutical regulatory authorities.
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Support audit and inspection processes.
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Follow international pharmacopeia standards.
π Educational Requirements
Candidates must meet the following academic criteria:
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MSc (Chemistry)
OR -
Doctor of Pharmacy (Pharm D)
Additional certifications in analytical chemistry, quality control, or pharmaceutical quality assurance will be considered an advantage.
πΌ Experience Requirements
Applicants should have:
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1β3 years of relevant experience in pharmaceutical quality control or stability testing.
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Practical exposure to stability programs.
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Experience working in a regulated pharmaceutical environment.
Fresh graduates with strong internships may not qualify unless they meet the minimum experience requirement.
π§ Required Technical Knowledge
To succeed in this role, candidates must have sound knowledge of:
π International Pharmaceutical Guidelines
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BP (British Pharmacopoeia)
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USP (United States Pharmacopeia)
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EP (European Pharmacopoeia)
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ICH (International Council for Harmonisation)
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WHO guidelines
Understanding regulatory documentation and validation standards is essential.
π§ Required Analytical Instrument Skills
Hands-on experience with the following instruments is mandatory:
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HPLC (High Performance Liquid Chromatography)
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FTIR (Fourier Transform Infrared Spectroscopy)
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UV Spectrophotometer
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pH Meter
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Other standard laboratory analytical equipment
Candidates should be able to:
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Calibrate instruments
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Troubleshoot minor technical issues
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Interpret chromatograms and analytical results
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Ensure proper documentation of test results
π 9 Powerful Reasons to Apply
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Reputable Pharmaceutical Employer β Join a trusted brand in Pakistanβs pharma sector.
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Stability Expertise Development β Gain specialized experience in stability programs.
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Exposure to International Guidelines β Work with BP, USP, EP, ICH & WHO standards.
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Advanced Instrument Handling β Strengthen HPLC and analytical testing expertise.
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Professional Growth β Clear path toward Senior QC roles and QA positions.
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Regulated Environment Experience β Enhance audit and compliance knowledge.
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Competitive Industry Positioning β Boost your pharmaceutical career profile.
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Karachi-Based Opportunity β Work in Pakistanβs major industrial hub.
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Meaningful Impact β Contribute to product quality and patient safety.
π Location: Karachi
This position is based in Karachi, Pakistanβs largest industrial and pharmaceutical hub. Working in Karachi provides:
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Access to leading pharmaceutical manufacturing facilities
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Exposure to regulatory inspections
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Networking with experienced industry professionals
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Long-term career growth in pharma sector
π° Compensation & Benefits
While the salary package is not explicitly mentioned, candidates can expect:
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Market-competitive salary
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Structured corporate environment
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Professional development opportunities
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Hands-on exposure to advanced laboratory systems
Compensation will depend on:
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Academic qualification
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Experience level
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Instrument proficiency
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Technical expertise
π€ Ideal Candidate Profile
You are the right candidate if you:
β Have 1β3 years of QC or stability experience
β Hold MSc (Chemistry) or Pharm D degree
β Possess strong documentation skills
β Understand pharmacopeia standards
β Have hands-on HPLC and analytical instrument experience
β Can work in a regulated and audit-ready environment
β Are detail-oriented and compliance-focused
π Career Growth Path
This role can lead to:
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Senior Officer QC
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Assistant Manager QC
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Quality Assurance Specialist
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Validation Officer
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Regulatory Affairs Executive
Experience gained in stability testing significantly strengthens your career prospects in the pharmaceutical industry.
π How to Apply
Interested candidates must apply through the QR code provided in the official job advertisement.
π Deadline: 8th March 2026
Application Tips:
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Update your CV to emphasize:
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Stability testing experience
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Instrument handling proficiency
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Knowledge of pharmacopeia guidelines
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Clearly mention your years of relevant experience.
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Highlight audit exposure and SOP compliance experience.
π€ Interview Preparation Guide
Prepare to discuss:
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Your experience with stability programs
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How you handle out-of-specification (OOS) results
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Instrument troubleshooting scenarios
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Compliance with GLP and GDP
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ICH stability guidelines
Be ready to explain analytical results and provide examples of documentation accuracy.
π Professional Expectations
As a QC professional, you will be expected to:
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Maintain strict data integrity
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Follow SOPs precisely
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Ensure accurate documentation
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Prepare for regulatory audits
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Maintain confidentiality and professionalism
π― Final Thoughts
The Officer / Senior Officer QC (Stability) role at Hilton Pharma is a strong opportunity for early-career pharmaceutical professionals seeking technical growth in quality control and stability testing.
If you are passionate about quality, compliance, and analytical excellence, this position offers the perfect platform to build your pharmaceutical career.
πΏ Contribute to Hope, Health & Happiness by ensuring medicines meet the highest standards of quality and safety.
π© Apply before 8th March 2026 and take the next step in your pharmaceutical career.
To apply for this job please visit lnkd.in.
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