
The SEARLE Company Ltd., a company that has stood for innovation, trust, and care for decades, is expanding its Quality Operations and Validation teams at its Karachi plants . We are currently hiring for two key positions in Quality Operations (Biotech) and Computer System Validation (CSV). If you are passionate about quality, compliance, and pharmaceutical excellence, this is your opportunity to grow with a dynamic organization.
Available Positions
1. Senior Lead Quality Operations (Biotech)
Job Scope:
- Develop and monitor Quality Objectives and departmental KPIs aligned with organization goals.
- Lead, mentor, and motivate the Quality Operations team to achieve quality and compliance objectives.
- Identify process gaps and recommend quality improvement initiatives.
- Ensure compliance of production activities with established quality standards and specifications.
- Ensure implementation, compliance, and continual improvement of the Quality Management System (QMS) and Health & Safety Management System in line with ISO and OHSAS requirements.
- Oversee the Vendor Qualification Program and ensure compliance with applicable standards.
- Identify training needs and organize quality-related training to strengthen team competency.
- Drive team performance management, employee development, and continuous improvement initiatives.
Job Specifications:
- Education: Pharm-D / M.Phil. in Biochemistry, Organic Chemistry, or Applied Chemistry.
- Experience: 10+ years of relevant experience in Quality Assurance/Quality Control within the pharmaceutical or biotech industry.
- Strong analytical background with proven experience in successfully handling internal and regulatory audits.
Apply: recruitment@searlecompany.com (Subject: Quality Ops Biotech)
2. Associate Manager – Validation & Qualification (CSV)
Job Scope:
- Validate GxP computerized systems in accordance with GAMP 5 guidelines .
- Prepare, review, and execute validation and qualification protocols/reports.
- Evaluate software changes, upgrades, and implementations through Change Control.
Requirements:
- Education: Pharm D, MSc. Chemistry/Applied Chemistry, or BE/BS in Computer Science, Software Engineering, or Computer Systems Engineering.
- Experience: 6–8 years of proven experience in Computer System Validation (CSV) within the pharmaceutical industry.
- Strong understanding of regulatory requirements, data integrity, and GMP compliance.
- Hands-on experience with SAP S/4HANA , LIMS , or other GxP computerized systems.
3. Management Trainee–Marketing
🎓 Qualification:
Fresh Marketing Graduates from reputable universitiesInternship experience in pharmaceutical industry (added advantage)
Why Join The SEARLE Company Ltd.?
- Industry Leader: Be part of a leading pharmaceutical company with a strong legacy of innovation, trust, and care .
- Biotech Growth: Work at Searle Biopharma, a growing biotech facility partnering with leading pharmaceutical companies .
- Career Growth: Opportunity to develop your career in Quality Operations or Computer System Validation.
- Professional Environment: Work in a state-of-the-art manufacturing facility.
- Competitive Compensation: Attractive salary and benefits package.
How to Apply:
Interested candidates should send their resume to: recruitment@searlecompany.com
Important:
- Mention the exact subject line as specified above:
- “Quality Ops Biotech” for the Senior Lead Quality Operations position
- “Associate Manager – Validation & Qualification (CSV)” for the CSV position
- “Management Trainee Marketing”
- Applications must be submitted by 20th August 2026.
- Only shortlisted candidates will be contacted.
Locations: Karachi (Port Qasim & SITE)
Application Deadline: 20th August 2026