Executive Regulatory Affairs Qarshi Industries Lahore

Executive Regulatory Affairs Qarshi Industries Lahore. Are you a Pharm-D graduate passionate about regulatory affairs and compliance in the pharmaceutical and natural products sector? Qarshi Industries (PVT.) Ltd., one of Pakistan’s leading FMCG and herbal healthcare companies, is hiring for the role of Executive Regulatory Affairs (International) at its Lahore office.

This is a fantastic opportunity for professionals with 2–3 years of relevant experience to advance their career by managing regulatory submissions, ensuring product compliance, and engaging with regulatory bodies both locally and internationally.

📍 Location: Lahore
📅 Application Deadline: 07 March 2026
📧 Application Email: [email protected]

🌟 About Qarshi Industries

Qarshi Industries is a well-established herbal and FMCG manufacturing company renowned for producing high-quality natural medicines, beverages, and consumer goods. The company emphasizes:

• Quality assurance and product safety

• Regulatory compliance across local and international markets

• Innovation in herbal and natural products

• Sustainable growth and corporate governance

Working at Qarshi provides exposure to cutting-edge regulatory practices in the pharmaceutical and herbal medicine sector.

📌 Position Overview

• Job Title: Executive Regulatory Affairs (International)

• Company: Qarshi Industries (PVT.) Ltd.

• Location: Lahore

• Education Required: Pharm-D

• Experience Required: 2–3 years relevant experience

• Age Range: 25–28 years

• Application Deadline: 07 March 2026

• How to Apply: Send CV to [email protected]

This role is ideal for detail-oriented, regulatory-focused professionals who can ensure that products meet national and international standards.

🎯 Job Summary

The Executive Regulatory Affairs (International) will be responsible for managing regulatory submissions, compliance, and communications with relevant authorities. The role ensures that Qarshi’s products meet regulatory requirements in all target markets and supports smooth product launches and ongoing compliance.

You will act as the primary contact for regulatory inquiries, audits, and inspections while preparing high-quality documentation for product approvals.

🔧 Key Responsibilities

1️⃣ Regulatory Liaison

• Maintain strong relationships with regulatory authorities locally and internationally

• Act as the point of contact for inspections, inquiries, and audits

• Provide timely updates on regulatory changes and requirements

2️⃣ Product Dossier Preparation

• Prepare CTD (Common Technical Document) and non-CTD dossiers for natural medicines

• Ensure accuracy and completeness of technical documentation

• Collaborate with R&D, production, and QA teams to gather necessary data

3️⃣ Label Compliance

• Ensure all labels for food products and herbal medicines comply with regulatory guidelines

• Review packaging and marketing materials for accuracy

• Monitor changes in local and international labeling laws

4️⃣ Regulatory Submissions

• Prepare, review, and submit documentation for:

  • New product registrations

  • Renewals and amendments

  • Product variations

• Track submission timelines and follow up with authorities

5️⃣ Documentation & Reporting

• Maintain accurate regulatory records for audits and inspections

• Support internal reporting and regulatory review meetings

• Ensure timely updates to regulatory databases and internal systems

🎓 Education & Experience Requirements

• Pharm-D degree (mandatory)

• 2–3 years of relevant regulatory experience in pharmaceuticals, herbal medicines, or FMCG

• Age preference: 25–28 years

• Familiarity with international regulatory submissions and guidelines is a plus

🧠 Skills Required

To succeed in this role, you should have:

✔ Technical & Regulatory Expertise

• Knowledge of CTD and non-CTD dossier preparation

• Understanding of labeling regulations for food and natural products

• Awareness of international regulatory frameworks

✔ Communication & Interpersonal Skills

• Clear written and verbal communication

• Ability to liaise with regulatory authorities professionally

• Collaborative mindset with internal departments

✔ IT & Analytical Skills

• Proficiency in MS Office

• Familiarity with AI tools for regulatory or data management is highly desirable

• Strong attention to detail and organizational skills

📍 Work Location: Lahore

The position is based in Lahore, offering:

• Access to Qarshi’s corporate and R&D facilities

• Exposure to a dynamic pharmaceutical and herbal product environment

• Opportunities for networking with regulatory authorities and industry professionals

🚀 Career Growth Opportunities

This role can open pathways to:

• Senior Regulatory Affairs Manager

• International Compliance Officer

• Product Registration Specialist

• Quality and Regulatory Lead

With experience, professionals may also move into cross-functional leadership roles, gaining broader exposure to product development and corporate strategy.

💼 Why This Role is Attractive

Here are 7 strong reasons to consider this opportunity:

1. Work with a leading herbal and FMCG company

2. Gain expertise in international regulatory affairs

3. Manage product registrations and dossier submissions

4. Ensure global regulatory compliance

5. Develop strong relationships with regulatory authorities

6. Enhance career prospects in pharmaceutical and FMCG sectors

7. Work in a professional corporate environment in Lahore

👩‍💼 Who Should Apply

Ideal candidates are:

• Pharm-D graduates with regulatory experience

• Professionals with experience in herbal medicines or natural product registrations

• Detail-oriented individuals capable of handling multiple submissions

• Candidates comfortable liaising with regulatory authorities

• Those looking to advance their career in international regulatory affairs

📧 How to Apply

Interested candidates should:

1. Prepare a detailed CV highlighting regulatory experience and dossier preparation

2. Mention the position title in the subject line

3. Send applications to: [email protected]

4. Apply before 07 March 2026

📝 Tips to Strengthen Your Application

To improve your chances:

• Highlight experience with CTD and non-CTD dossiers

• Include familiarity with food and herbal product labeling regulations

• Showcase experience in submissions, renewals, and amendments

• Demonstrate communication and coordination skills

• Mention any exposure to AI tools for documentation or regulatory compliance

⚡ The Growing Importance of Regulatory Affairs

Regulatory affairs is a critical function in pharmaceutical and FMCG industries:

• Ensures legal compliance in all product markets

• Prevents product recalls or delays due to non-compliance

• Supports market expansion internationally

• Builds trust with consumers and regulators

Qarshi Industries provides a platform to grow as a regulatory professional and gain international exposure.

🎯 Final Thoughts – Are You the Right Fit?

If you have:

• A Pharm-D degree

• 2–3 years of regulatory experience

• Strong documentation, communication, and compliance skills

• Passion for international regulatory affairs

…then this role at Qarshi Industries (PVT.) Ltd. in Lahore could be your next big career step.

📅 Deadline: 07 March 2026
📧 Email: [email protected]

Take this opportunity to advance your regulatory career, ensure product compliance, and gain international exposure with a leading herbal and FMCG company.

Do you want me to expand this into a full 1200+ word article with detailed insights into CTD/non-CTD submissions, compliance KPIs, and international regulatory interactions so it reads as a complete career guide for applicants?