Senior Manager Pharmevo Karachi

Senior Manager Pharmevo Karachi. At **Pharmevo (Evodian Group)**, we believe that excellence isn’t accidental—it’s intentional. Driven by our inspiring vision, **“Our Dream, A Healthier Society,”** and guided by our core values **ITREE (Integrity, Trust, Respect, Ethics & Excellence)**, we continue to soar higher in Pakistan’s pharmaceutical landscape.

As one of the **top pharmaceutical companies in Pakistan**, Pharmevo has earned its reputation through **socially responsible marketing**, uncompromised quality standards, and an unwavering commitment to patient safety. To strengthen our Quality function and support future growth, we are excited to announce a senior leadership opportunity.

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## 🔍 Position Open: **Senior Manager – Quality Control**

This is not just a job—it’s a **leadership role** for professionals who want to shape quality systems, mentor teams, and ensure that life-saving medicines meet **global regulatory standards**.

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## 📍 Job Location
**Port Qasim, Karachi**

A strategically important manufacturing hub offering exposure to large-scale pharmaceutical operations and regulatory-facing responsibilities.

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## 🧭 About the Role

As **Senior Manager – Quality Control**, you will be responsible for **end-to-end QC laboratory leadership**, ensuring compliance, efficiency, and continuous improvement across all quality control operations. You will act as a **key decision-maker**, directly influencing product quality, regulatory readiness, and organizational credibility.

This role is ideal for seasoned QC professionals who have **independently led QC labs**, handled audits, and worked extensively within **cGMP-regulated environments**.

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## 🛠️ Key Responsibilities (What You’ll Be Doing)

### **1. QC Laboratory Leadership**
– Lead and manage **day-to-day Quality Control laboratory operations**.
– Ensure **timely testing** of:
– Raw materials
– Finished pharmaceutical products
– Packaging materials
– Utilities

### **2. Stability Studies Management**
– Oversee the **site stability studies program**.
– Ensure **100% testing of stability time points** strictly as per approved stability schedules.
– Review and evaluate stability trends to support product shelf-life and regulatory submissions.

### **3. Regulatory & Compliance Excellence**
– Ensure **strict compliance** with:
– **cGMP & cGLP**
– **Data Integrity (ALCOA++)**
– **DRAP, FDA, EMA, WHO** guidelines
– Prepare QC systems for **internal, external, and regulatory audits**.

### **4. Documentation & SOP Governance**
– Review, approve, and implement:
– SOPs
– Specifications
– Analytical protocols
– Test methods
– Analytical and investigation reports

### **5. Investigations & CAPA Management**
– Handle and close:
– **OOS (Out of Specification)**
– **OOT (Out of Trend)**
– Deviations
– Change controls
– **CAPAs**
– Ensure investigations are **timely, data-driven, and effective**.

### **6. Risk Management**
– Identify laboratory risks proactively.
– Perform **risk assessments** and implement mitigation strategies as required.

### **7. Instrument & Method Oversight**
– Supervise and support lab teams in:
– Instrument qualification
– Calibration and validation
– Preventive maintenance
– Manage:
– Analytical method validation
– Method verification
– Method transfer activities

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## 🎓 Qualification & Experience Requirements

To excel in this role, you should bring both **academic strength** and **extensive hands-on experience**.

### **Education**
– **Bachelor’s or Master’s degree in Science** (Chemistry, Pharmacy, or related discipline).

### **Experience**
– **Minimum 12 years of experience** in **Pharmaceutical Quality Control** functions.
– At least **3 years of independent QC laboratory leadership** experience.
– Proven exposure to:
– GMP environments
– Regulatory inspections
– Complex QC operations

### **Technical & Professional Skills**
– Strong experience with **ISO-17025 and GMP audits**.
– Expertise in:
– Analytical techniques
– Laboratory instrumentation
– Data integrity systems
– Laboratory safety standards
– Computerized laboratory systems (LIMS, CDS, etc.)

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## 🌟 Why Join Pharmevo? (What’s In It for You)

### ✅ Accelerated Career Growth
Work in a **leadership-driven environment** where talent is recognized and promoted.

### ✅ Exciting Perks & Benefits
Competitive compensation, professional exposure, and a supportive corporate culture.

### ✅ Impactful Work
Your work directly contributes to **public health and patient safety** across Pakistan and beyond.

### ✅ Values-Driven Organization
Be part of a company that lives by **Integrity, Trust, Respect, Ethics & Excellence**—not just on paper, but in practice.

### ✅ Life-Altering Experience
This is more than a job—it’s a chance to **shape quality systems**, **mentor future leaders**, and **leave a legacy** in the pharmaceutical industry.

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## 📩 How to Apply

If you’re ready to elevate your career and meet global quality benchmarks, we want to hear from you.

📧 **Send your resume to:**
**[email protected]**

📅 **Application Deadline:**
**9th February 2026**

> *Tip:* Mention **“Senior Manager – Quality Control”** in the subject line of your email for faster processing.

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## 🏢 About Pharmevo (Evodian Group)

**Pharmevo** stands among Pakistan’s leading pharmaceutical companies, driven by innovation, ethical practices, and a deep commitment to healthcare excellence. Through **socially responsible marketing** and world-class manufacturing standards, Pharmevo continues to make medicines safer, more accessible, and more effective.

**Our Dream, A Healthier Society** is not just a slogan—it’s our promise.

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🚀 Ready to Fly Higher?
If you believe your vision goes beyond limits and your standards align with global excellence, **this is your moment**. Join Pharmevo and redefine what quality leadership looks like in Pakistan’s pharmaceutical industry.