Eris Bionxt Private Limited is inviting applications for multiple vacancies in Quality Assurance (QA) and Quality Control (QC) departments at its sterile injectable manufacturing facility in Bhopal, Madhya Pradesh. This hiring drive is focused on experienced professionals who have worked in injectable or sterile pharmaceutical environments and are looking to grow in regulated pharma operations.
This opportunity is ideal for candidates aiming to build strong careers in pharmaceutical quality systems, regulatory compliance, and sterile manufacturing processes. Working in a GMP-compliant injectable facility provides excellent exposure to high-end quality standards and global regulatory practices.
Company Overview
Eris Bionxt Private Limited is part of the reputed Eris Lifesciences group, known for its expanding presence in pharmaceutical manufacturing and specialty healthcare products. The company focuses on innovation, compliance, and delivering high-quality medicines across therapeutic segments.
The Bhopal facility is a modern sterile injectable plant designed to operate under stringent GMP guidelines, offering professionals hands-on experience with advanced pharmaceutical quality systems.
Job Roles & Responsibilities
Quality Assurance (QA) โ Executive / Officer
- Perform IPQA activities and in-process quality checks
- Handle documentation such as SOPs, BMR/BPR, and QMS records
- Ensure compliance with GMP and regulatory standards
- Participate in internal and external audits
- Manage deviations, CAPA, and change control processes
Quality Control (QC) โ Executive / Officer
- Conduct analysis of raw materials, intermediates, and finished products
- Operate analytical instruments and ensure accurate testing
- Maintain GLP compliance and proper documentation
- Support stability studies and method validation
- Ensure data integrity and regulatory compliance
Eligibility & Qualifications
Educational Qualification
- B.Pharm / M.Pharm
- B.Sc / M.Sc (Life Sciences)
Relevant Fields
- Pharmaceutical Sciences
- Analytical Chemistry
- Microbiology
- Industrial Pharmacy
- Quality Assurance / Regulatory Affairs
Experience Required
- 2 to 6 years of experience preferred
- Must have experience in injectable or sterile pharma plants
Skills Required
- Strong knowledge of GMP and GLP guidelines
- Experience in sterile manufacturing environments
- Documentation and audit handling expertise
- Analytical skills (for QC roles)
- Understanding of quality systems and compliance
Job Location & Salary
Location
- Bhopal, Madhya Pradesh
Salary
- โน3.5 LPA โ โน7.5 LPA (based on experience and role)
- Additional benefits as per company policy
How to Apply
Interested candidates can send their updated CV to:
Make sure your resume clearly highlights your experience in injectable or sterile pharmaceutical manufacturing.
