Rusan Pharma Hiring for QA, Engineering, Production & AQA Roles | API Facility Jobs in Ankleshwar

Rusan Pharma is hiring for QA, Engineering, Production, and AQA roles at its USFDA-approved API plant in Ankleshwar. Apply now via email. B.Sc./M.Sc. graduates eligible.

🚀 Rusan Pharma Job Openings 2025 | QA, Engineering, Production & AQA Roles in Ankleshwar

Rusan Pharma Ltd., a trusted name in the global pharmaceutical industry, is hiring for multiple departments at its US FDA-approved API manufacturing facility in Ankleshwar, Gujarat. If you’re an experienced pharmaceutical professional with a background in QA, Production, Engineering, or Analytical Quality Assurance (AQA), this is an exciting opportunity to advance your career in a GMP-compliant and internationally certified environment.

🏭 About Rusan Pharma Ltd.

Rusan Pharma is a global pharmaceutical organization dedicated to the development and supply of high-quality Active Pharmaceutical Ingredients (APIs), formulations, and specialty treatments. With approvals from USFDA, WHO-GMP, and other global regulatory agencies, Rusan Pharma is a key player in pain management, addiction therapy, and critical care medications.

Its Ankleshwar API plant is one of the company’s flagship manufacturing hubs, designed for regulatory excellence, cGMP adherence, and sustainable manufacturing practices.

📍 Job Location

Rusan Pharma Ltd. Plot No. 6406, Nr. Hoechst Chowkdi, GIDC, Ankleshwar, Gujarat – 393002

📌 Current Job Openings at Rusan Pharma

1️⃣ Quality Assurance (QA)

• Position: Sr. Officer / Executive

• Experience: 3–7 years (API QA experience mandatory)

• Qualification: B.Sc. / M.Sc. (Chemistry or related fields)

• Department: Quality Assurance

Key Responsibilities:

• Handle documentation, deviation, CAPA, and change control.

• Ensure compliance with cGMP, ICH, and USFDA guidelines.

• Support internal and regulatory audits.

• Maintain Quality Management System (QMS) compliance.

2️⃣ Engineering (GMP Coordinator)

• Position: GMP Coordinator

• Experience: 5–7 years (API manufacturing experience required)

• Qualification: B.Sc. / M.Sc.

• Department: Engineering

Key Responsibilities:

• Coordinate and ensure GMP compliance in equipment and utilities.

• Prepare and review engineering documentation and qualification protocols.

• Liaise with QA/Validation/Production for project execution.

• Support audits and preventive maintenance programs.

3️⃣ Production (GMP Coordinator)

• Position: GMP Coordinator

• Experience: 5–7 years (experience in API production mandatory)

• Qualification: B.Sc. / M.Sc.

• Department: Production

Key Responsibilities:

• Oversee daily production activities with focus on GMP compliance.

• Coordinate production documentation and batch record reviews.

• Facilitate production audits and quality checks.

• Ensure timely batch completion and resource optimization.

4️⃣ Analytical Quality Assurance (AQA)

• Position: Executive / Assistant Manager

• Experience: 5–10 years (API QA with analytical experience required)

• Qualification: B.Sc. / M.Sc.

• Department: Analytical QA

Key Responsibilities:

• Review of analytical documents (HPLC, GC, Stability, etc.).

• Ensure data integrity and audit trail compliance.

• Coordinate with QC and regulatory teams.

• Prepare documentation for USFDA/MHRA compliance.

🌟 Why Join Rusan Pharma?

• 🏢 Work in a US FDA-approved manufacturing facility

• 📈 Career growth with structured training and upskilling

• 🌐 Opportunity to contribute to global pharmaceutical exports

• 💼 Competitive salaries, performance incentives, and employee-friendly policies

• 🤝 Culture of quality, integrity, and innovation

📧 How to Apply

Interested candidates can share their updated resume via email to: 📩 mitesh.maharaj@rusanpharma.com 👉 Subject Line: Application for [Job Title] – Ankleshwar

📝 Application Process

🧪 Build Your Career in Pharma Manufacturing

Whether you’re an analytical expert, production professional, GMP coordinator, or QA associate, Rusan Pharma offers a career path with global exposure, regulatory challenges, and technical advancement. Join a team that is passionate about ensuring safe and compliant pharmaceutical products for global markets.