QUALITY CONTROL MANAGER (QCM)

Lusynco; Islamabad; On-site; PKR 2,000,000 - 3,000,000; Full time

Job summary

Lusynco in Islamabad is seeking a seasoned Quality Control Manager to lead QC operations at the Rawat facility. The role requires an analytical mindset, strong leadership, and deep regulatory knowledge.

You will oversee laboratory testing of materials and finished products, ensure cGLP/cGMP compliance, mentor staff, and prepare for internal audits and external inspections.

Qualifications

• 10+ years of progressive experience in pharmaceutical quality control.
• Strong command of CT Dossier compilation and regulatory requirements.
• Proven leadership and ability to mentor QC staff.
• Experience with cGMP/cGLP regulatory guidelines.

Responsibilities

• Oversee laboratory operations and ensure strict quality standards.
• Lead internal quality audits and coordinate external inspections.
• Develop and enforce compliant testing protocols for materials and products.
• Mentor staff and optimize workflow and safety.

Skills

Analytical skills

Leadership

Regulatory knowledge

Job description

Quality Control Manager

A prominent pharmaceutical organization is seeking a highly experienced and technically proficient Quality Control Manager to lead its QC operations at their facility in Rawat, Islamabad. This senior-level leadership role requires an analytical mindset, robust management capabilities, and an advanced understanding of regulatory compliance. The ideal candidate will be responsible for overseeing laboratory operations, enforcing strict quality standards, and driving regulatory excellence.

CT Dossier Expertise

Must possess a comprehensive, authoritative command over Common Technical Document (CT) Dossiers.

Quality Oversight

Oversee comprehensive testing of raw materials, in-process components, and finished pharmaceutical products to guarantee compliance with international standards.

Regulatory Compliance

Ensure all laboratory testing procedures adhere to current Good Laboratory Practices (cGLP), Good Manufacturing Practices (cGMP), and national regulatory guidelines.

Team Leadership

Manage, mentor, and train the quality control laboratory staff, optimizing workflow efficiency and operational safety.

Audit Readiness

Direct internal quality audits and serve as a key point of contact during external regulatory inspections.

Preferred Profile

Tenure: A minimum of 10 years of progressive experience within a pharmaceutical Quality Control environment.

Skills: Exceptionally strong analytical, organizational, and decision‑making skills paired with an expert-level understanding of dossier compilation and regulatory requirements.

Salary

• A market‑competitive salary package tailored explicitly to the candidate's professional experience, background, and specific skill set.

How to Apply

Qualified professionals who meet the 10-year experience criteria are invited to apply by submitting their credentials directly:

• WhatsApp: Share your updated CV with the recruitment team at 03295466071.