Aykon Biosciences Hiring | Job Openings for QA, QC, Production & Regulatory Affairs [B.Pharm/M.Pharm]

Apply now for pharmaceutical jobs at Aykon Biosciences in Kheda, Gujarat. Openings for Quality Control, Quality Assurance, Production & Regulatory Affairs professionals with B.Pharm or M.Pharm. Advance your pharma career in a cGMP-compliant injectable manufacturing facility.

🚀 Aykon Biosciences Pharma Job Openings in Kheda | Apply Now for QA, QC, Production & Regulatory Affairs Roles – 2025

Aykon Biosciences Pvt. Ltd. is hiring passionate and skilled professionals for its injectable manufacturing facility in Kheda, Gujarat. If you’re a B.Pharm or M.Pharm graduate with 1–2 years of relevant experience in Quality Control (QC), Quality Assurance (QA), Production, or Regulatory Affairs, here’s your opportunity to join a fast-growing pharmaceutical company focused on innovation and global quality standards.

🧪 About Aykon Biosciences Pvt. Ltd.

Founded in 2021, Aykon Biosciences is an emerging leader in the injectable formulations space, specializing in Small Volume Parenterals (SVP) including ampoules and pre-filled syringes (PFS). The company’s state-of-the-art facility in Kheda, Gujarat, is built to meet cGMP and international regulatory standards like USFDA and MHRA, enabling high-quality, affordable injectable medicines for the global market.

🌟 Why Join Aykon Biosciences?

✅ Work in a modern injectable facility designed to meet international quality norms
✅ Collaborate with cross-functional teams and regulatory authorities
✅ Competitive pay structure and comprehensive benefits
✅ Exposure to cGMP practices and global regulatory compliance
✅ Career growth in a high-demand niche: injectable pharmaceuticals

🏢 Job Location

📍 Kheda, Gujarat
Address: Survey No. 86/1-2-3, Village Sarali, Ahmedabad–Indore Highway, Tal: Kathlal, Dist: Kheda, Gujarat – 387630
A rapidly expanding facility equipped with advanced manufacturing and testing infrastructure.

📋 Available Job Openings – 2025

Aykon Biosciences is currently hiring for 8 positions across 4 major departments. All roles are full-time and onsite at the Kheda facility.

1️⃣ Quality Control (QC) Specialist – 2 Vacancies

Qualification: B.Pharm or M.Pharm
Experience: 1–2 years in Quality Control in pharmaceutical manufacturing

Responsibilities:

• Conduct analytical testing of raw materials, in-process and finished products

• Operate HPLC, UV spectrophotometer, and other analytical instruments

• Maintain quality records in line with Good Documentation Practices (GDP)

• Prepare for and support regulatory audits and inspections

Key Skills:

• Knowledge of analytical techniques and regulatory guidelines

• Experience with cGMP, GLP, and documentation protocols

• Attention to detail and ability to maintain data integrity

2️⃣ Quality Assurance (QA) Specialist – 2 Vacancies

Qualification: B.Pharm or M.Pharm
Experience: 2 years in QA or related pharmaceutical functions

Responsibilities:

• Implement and monitor Standard Operating Procedures (SOPs)

• Conduct internal audits, handle deviation reports, and manage CAPAs

• Review BMRs/BPRs and ensure QMS compliance

• Coordinate with production and QC for quality compliance

Key Skills:

• Strong knowledge of quality systems and risk management

• Hands-on experience with regulatory inspections

• Excellent organizational and interpersonal communication skills

3️⃣ Production Specialist – 2 Vacancies

Qualification: B.Pharm or M.Pharm
Experience: 2 years in sterile/injectable pharmaceutical manufacturing

Responsibilities:

• Supervise and execute manufacturing activities for injectable products

• Operate equipment like vial filling lines, ampoule filling, autoclaves

• Maintain batch manufacturing records (BMR) and ensure cGMP compliance

• Optimize production processes for efficiency and safety

Key Skills:

• Knowledge of sterile formulation processes

• Understanding of cleanroom behavior and contamination control

• Team leadership and production line optimization

4️⃣ Regulatory Affairs Specialist – 2 Vacancies

Qualification: B.Pharm or M.Pharm
Experience: 1–2 years in Regulatory Affairs in a pharmaceutical company

Responsibilities:

• Compile and submit regulatory dossiers for international markets (USFDA, MHRA, WHO-GMP)

• Prepare and review Product Dossiers, DMFs, and CTDs

• Coordinate with R&D, QA, and production for data gathering and compliance

• Respond to queries from regulatory bodies and prepare annual reports

Key Skills:

• Deep understanding of regulatory frameworks and submission guidelines

• Experience with pharma documentation systems

• Strong communication, document management, and problem-solving skills

🎯 Why These Roles Matter

Whether it’s ensuring stringent product quality, maintaining compliance with global standards, or enabling smooth regulatory approvals, these roles are critical to Aykon’s mission of building a trusted pharmaceutical brand.

Your work will directly contribute to:

• Patient safety

• Product innovation

• Regulatory success

• Market access in global regions

🎁 Benefits of Joining Aykon Biosciences

• 💼 Competitive salary packages benchmarked to the industry

• 📚 Learning & development programs for continuous skill enhancement

• 🌐 Exposure to global pharma markets and regulatory practices

• 🧪 Work with cutting-edge injectable manufacturing technology

• 🤝 Supportive team culture with transparent leadership

📨 How to Apply

📧 Send your updated resume to: careers@aykon.in
📝 Subject Line: Application for [Job Title] – Kheda Facility

Tip: Mention your experience, notice period, and current location in your email for faster processing.

🔄 Application Process

🏭 About Our Kheda Facility

The Aykon Biosciences manufacturing site in Kheda, Gujarat, spans several acres and is equipped for sterile injectable production, meeting international standards. With a focus on PFS (Pre-Filled Syringes) and ampoules, the site supports both domestic and export markets, positioning itself as a strategic hub for injectable pharmaceuticals.

🌐 Learn More

🔗 Company Website
🔗 Careers at Aykon

💬 Join Aykon, Shape the Future of Injectables

If you’re ready to take your pharma career to the next level in a growth-centric, globally aligned company, Aykon Biosciences is your destination. With roles in QC, QA, Production, and Regulatory Affairs, this is your chance to build expertise in sterile manufacturing and contribute to global healthcare.

Apply now and be part of a company where quality meets innovation.