Eris Bionxt Hiring 2025: Multiple Job Openings in QA, QC, Production, Regulatory & More

Eris Bionxt Pvt Ltd is hiring for multiple roles in QA, QC, Production, Microbiology, Engineering, and Regulatory Affairs at its sterile injectable facility in Bhopal. Apply by July 15, 2025. Experience in PFS, MAB, or cartridge lines preferred.

💼 Eris Bionxt Careers 2025: Hiring for QA, QC, Production, Regulatory, Microbiology & More in Bhopal | Apply Now

Eris Bionxt Pvt Ltd, a rapidly growing subsidiary of Eris Lifesciences Ltd, is urgently hiring across departments including Quality Assurance (QA), Quality Control (QC), Microbiology, Production, Engineering, Packing, Warehouse, IT Services, and Regulatory Affairs at its sterile injectable facility in Bhopal, Madhya Pradesh.

If you’re looking to build a rewarding career in biosimilar injectable manufacturing, especially in areas like Pre-Filled Syringes (PFS), Monoclonal Antibodies (MAB), or cartridge line operations, now is the time to join one of India’s most promising sterile facilities.

🌐 About Eris Bionxt Pvt Ltd

Established in 2020, Eris Bionxt Pvt Ltd is a specialized injectable unit under Eris Lifesciences Ltd, ranked #21 in the Indian pharmaceutical market. Located in Mandideep Industrial Area, Bhopal, Eris Bionxt is a WHO-GMP-certified and USFDA-aligned facility focused on developing and producing biosimilars.

The facility supports formulation, filling, lyophilization, and packaging operations, with a focus on sterility assurance and compliance. Eris Bionxt is supported by the strong commercial and distribution network of Eris Lifesciences and benefits from recent injectable portfolio acquisitions, including assets from Biocon.

🔗 Learn More About Eris Bionxt Careers

🏭 Current Job Openings in Bhopal (Multiple Departments)

Eris Bionxt is inviting candidates with relevant sterile injectable plant experience in PFS, MAB, or cartridge lines for the following roles:

🧪 1. Quality Control (QC)

• Skills: HPLC, GC, Stability testing, Analytical method validation, QMS handling

• Experience: 2–8 years

• Qualification: B.Pharm, M.Pharm, M.Sc. (Chemistry/Biotech)

• Key Responsibilities:

  • Raw material, in-process & finished product testing

  • Stability studies & analytical documentation

  • Compliance with GMP/GLP practices

✅ 2. Quality Assurance (QA)

• Skills: IPQA, Batch review, QMS, Process validation

• Experience: 2–8 years

• Qualification: B.Pharm, M.Pharm, M.Sc.

• Key Responsibilities:

  • In-process checks, GMP documentation, deviation & CAPA handling

  • BMR/BPR review & approval

  • Audit preparation & support

🔬 3. Microbiology

• Skills: BET, Sterility testing, EM, cleanroom classification

• Experience: 2–6 years

• Qualification: M.Sc. (Microbiology/Biotech)

• Key Responsibilities:

  • Microbial testing of injectables

  • Cleanroom & environmental monitoring

  • Water testing, personnel monitoring

🛠️ 4. Engineering

• Skills: PLC/SCADA systems, equipment calibration, preventive maintenance

• Experience: 3–8 years

• Qualification: ITI, Diploma, B.Tech (Mechanical/Electrical)

• Key Responsibilities:

  • Operation & maintenance of sterile manufacturing equipment

  • HVAC, compressed air, purified water system oversight

  • GMP documentation for engineering activities

🧫 5. Production

• Skills: Aseptic processing, filling, lyophilization, PFS, cartridge line

• Experience: 2–8 years

• Qualification: Diploma, B.Sc., B.Tech

• Key Responsibilities:

  • Cleanroom operations including compounding & filtration

  • Filling & sealing of sterile injectables

  • Batch manufacturing documentation

📦 6. Packing

• Skills: Primary/Secondary packing, documentation, GMP practices

• Experience: 1–5 years

• Qualification: ITI, Diploma, B.Sc.

• Key Responsibilities:

  • PFS & cartridge packing operations

  • Blister/sealing line handling

  • Line clearance and batch reconciliation

🏬 7. Warehouse

• Skills: Material issuance, raw material handling, inventory management

• Experience: 1–5 years

• Qualification: Any Graduate

• Key Responsibilities:

  • Goods receipt, issue & storage in GMP environment

  • SAP/ERP system usage

  • Store audits and stock accuracy

💻 8. IT Services

• Skills: ERP, IT infrastructure support, Data integrity compliance

• Experience: 2–6 years

• Qualification: B.Tech (IT/CS), BCA

• Key Responsibilities:

  • Maintenance of systems related to manufacturing & QA/QC

  • Ensuring data integrity and network uptime

  • Support for equipment integration & software validation

🧾 9. Regulatory Affairs

• Skills: DMF, CTD/eCTD submissions, USFDA/EMA guidelines

• Experience: 3–8 years

• Qualification: B.Pharm, M.Pharm, M.Sc.

• Key Responsibilities:

  • Regulatory documentation for injectables

  • Responding to deficiency letters

  • Interacting with global regulatory authorities

📨 Application Process

🌟 Why Join Eris Bionxt Pvt Ltd?

✅ Advanced Sterile Facility

Work in a WHO-GMP-compliant sterile injectable plant designed for global compliance and excellence.

💉 Focus on Biosimilars

Join projects involving Pre-Filled Syringes (PFS), MABs, and cartridge line technologies—sectors seeing rapid global demand.

🌍 Growth with a Trusted Brand

Be part of Eris Lifesciences, a company recognized for its cardio-metabolic portfolio, strong financial growth, and strategic acquisitions like Biocon’s injectables.

👥 Collaborative Culture

Work with 116+ employees in a team-driven environment rated 3.7/5 for work-life balance on AmbitionBox.

💰 Competitive Compensation

Enjoy attractive salaries, performance-based incentives, and long-term career growth in a high-demand segment.

📅 Important Dates

🚀 Final Call to Apply

If you’re an experienced professional in sterile injectable manufacturing, this is your opportunity to join a USFDA-aligned biosimilar company driving pharmaceutical innovation in India.

📧 Send your CV to: hr@erisbionxt.com

📍 Location: Bhopal, Madhya Pradesh

🗓️ Deadline: Apply before July 15, 2025