Aspin Pharma, an OBS Group Company, has announced exciting career opportunities for experienced Quality Assurance (QA) and Quality Control (QC) professionals. The company is seeking qualified candidates for Officer, Executive, and Senior Executive positions to strengthen its pharmaceutical quality operations.
This recruitment drive offers an excellent opportunity for candidates with GMP, GLP, regulatory compliance, laboratory testing, and quality management experience to join a growing pharmaceutical organization.
Available Positions
1. Officer / Executive / Sr. Executive – Quality Assurance (QA)
Key Responsibilities
Strong knowledge of GMP, GLP, and regulatory compliance.
Hands-on experience in:
Documentation management
Quality checks
Internal audits
SOP implementation
Conduct in-process quality checks and batch release activities.
Review and maintain:
QA/QC documentation
Standard Operating Procedures (SOPs)
Quality records
Support continuous improvement initiatives within manufacturing and quality systems.
2. Officer / Executive / Sr. Executive – Quality Control (QC)
Key Responsibilities
Perform routine testing of semi-finished and finished pharmaceutical products.
Verify analytical equipment performance on a daily basis.
Maintain accurate laboratory records and ensure compliance with GMP and GLP requirements.
Support quality investigations and deviation handling.
Collaborate with Production and QA teams.
Assist in process improvement and quality enhancement initiatives.
Educational Qualification
Candidates should possess any of the following qualifications:
Pharm-D
M.Sc. (Chemistry)
Experience Requirement
QA/QC Positions
Officer / Sr. Officer: 1–2 Years
Executive / Sr. Executive: 2–4 Years
Experience should be in a pharmaceutical quality environment.
Required Competencies
Successful candidates should demonstrate:
Drive for results
Customer focus
Teamwork and collaboration
Innovation mindset
Business acumen
Strong communication skills
Training & Knowledge Requirements
Applicants should have good knowledge of:
GMP (Good Manufacturing Practices)
GLP (Good Laboratory Practices)
Regulatory Guidelines
DRAP Requirements
ICH Guidelines
Laboratory Equipment Handling
Manufacturing Processes
MS Office Applications
Job Location
Head Office, Sector 20, Landhi Town, Karachi
Application Process
Interested candidates should send their updated resume to:
careers@aspin.com.pk
Important: Mention the applied position in the email subject line.
Last Date to Apply
23 June 2026
Only shortlisted candidates will be contacted for further recruitment processes.
Why Join Aspin Pharma?
Aspin Pharma is recognized for its commitment to pharmaceutical quality, regulatory compliance, and operational excellence. Working with Aspin Pharma provides professionals with opportunities to enhance their expertise in QA and QC functions while contributing to high-quality pharmaceutical manufacturing standards.
Technical FAQs
1. What is the difference between GMP and GLP in pharmaceutical operations?
GMP (Good Manufacturing Practices) ensures products are consistently manufactured and controlled according to quality standards, whereas GLP (Good Laboratory Practices) focuses on maintaining the quality and integrity of laboratory testing and data.
2. What is the role of batch release in Quality Assurance?
Batch release involves reviewing manufacturing and testing records to verify that a product meets predefined quality standards before being approved for market distribution.
3. Why are SOPs important in pharmaceutical manufacturing?
SOPs provide standardized instructions for processes, ensuring consistency, regulatory compliance, product quality, and employee safety.
4. What analytical instruments are commonly used in Quality Control laboratories?
QC laboratories commonly use:
HPLC
GC
UV-Visible Spectrophotometer
FTIR
Dissolution Test Apparatus
pH Meter
Karl Fischer Titrator
5. What are ICH guidelines and why are they important?
The International Council for Harmonisation (ICH) develops globally accepted guidelines for pharmaceutical quality, safety, efficacy, and regulatory requirements, helping companies maintain international compliance standards.

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