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QA & QC Executive Job at Eris Bionxt Apply Now

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Eris Bionxt QA QC Executive jobs 2026 in Bhopal. Check eligibility, salary, sterile pharma experience, and apply via email today.

Introduction

If you have experience in sterile pharmaceutical manufacturing and want to grow in quality operations, this opportunity is highly valuable. The QA & QC Executive job at Eris Bionxt Private Limited offers a chance to work in a modern injectable facility in Bhopal. It is ideal for professionals looking to strengthen their expertise in GMP compliance, regulatory systems, and advanced pharmaceutical quality processes.


Job Overview

DetailsInformation
Job TitleQA & QC Executive
Company NameEris Bionxt Private Limited
LocationBhopal, Madhya Pradesh
Employment TypeFull-Time
DepartmentQuality Assurance & Quality Control
Experience Required2–6 Years
EducationB.Pharm, M.Pharm, B.Sc, M.Sc
Salaryβ‚Ή3.5 LPA – β‚Ή7.5 LPA

Company Overview

Eris Bionxt Private Limited is a part of the well-known Eris Lifesciences group, recognized for its strong presence in the Indian pharmaceutical market. The company focuses on delivering high-quality medicines while maintaining strict compliance with global regulatory standards.

Its Bhopal facility is a state-of-the-art sterile injectable plant designed to meet GMP guidelines, offering professionals exposure to advanced manufacturing systems and regulatory practices.


Job Location & Employment Type

  • Location: Bhopal, Madhya Pradesh
  • Employment Type: Full-Time
  • Industry: Pharmaceutical Manufacturing (Sterile Injectables)

Open Positions / Department Details

Multiple openings are available in:

  • Quality Assurance (QA) – Executive / Officer
  • Quality Control (QC) – Executive / Officer

These roles are critical for maintaining product quality, compliance, and regulatory standards in sterile injectable manufacturing.


Key Roles & Responsibilities

Quality Assurance (QA)

  • Perform IPQA activities and in-process quality checks
  • Prepare and review SOPs, BMR/BPR, and QMS documentation
  • Ensure compliance with GMP and regulatory guidelines
  • Participate in internal and external audits
  • Handle deviation management, CAPA, and change control
READ THIS  Cadila Pharmaceuticals Hiring for Production / QC / QA

Quality Control (QC)

  • Analyze raw materials, intermediates, and finished products
  • Operate analytical instruments for testing and validation
  • Maintain GLP compliance and proper documentation
  • Support stability studies and method validation
  • Ensure data integrity and regulatory compliance

Eligibility Criteria

Education

  • B.Pharm / M.Pharm
  • B.Sc / M.Sc in relevant disciplines

Relevant Fields

  • Pharmaceutical Sciences
  • Analytical Chemistry
  • Microbiology
  • Industrial Pharmacy
  • Quality Assurance / Regulatory Affairs

Experience

  • 2 to 6 years of experience in QA/QC roles
  • Mandatory experience in sterile or injectable pharmaceutical plants

Skills Required

  • Strong understanding of GMP and GLP guidelines
  • Experience in sterile manufacturing environments
  • Documentation and audit handling expertise
  • Analytical and problem-solving skills
  • Knowledge of quality systems and compliance

Salary & Benefits

  • Salary Range: β‚Ή3.5 LPA – β‚Ή7.5 LPA
  • Additional benefits as per company policy
  • Work in a GMP-compliant injectable facility
  • Exposure to global regulatory standards
  • Career growth in QA/QC and regulatory domains
  • Training and skill enhancement opportunities

Selection Process

The selection process generally includes:

  1. Resume Screening
  2. Technical Interview
  3. HR Discussion
  4. Final Selection

How to Apply

Interested candidates can apply via email application:

πŸ“§ Send your updated CV to: hr@erisbionxt.com

Make sure your resume clearly highlights your experience in sterile or injectable pharmaceutical manufacturing.


Important Dates

  • Published On: 10 April 2026
  • Apply early as positions may be filled quickly

Why Apply for This Job?

The QA & QC Executive job at Eris Bionxt Private Limited is a great opportunity for experienced pharma professionals aiming to advance in sterile manufacturing and quality systems.

  • Work in a modern injectable manufacturing facility
  • Gain exposure to GMP, GLP, and regulatory audits
  • Strengthen expertise in QA/QC and compliance systems
  • Opportunity to grow into senior quality and regulatory roles
  • Be part of a reputed pharmaceutical group
READ THIS  Regulatory Affairs Jobs at Provis Biolabs

FAQs

1. Who can apply for this QA & QC Executive job?

Candidates with B.Pharm, M.Pharm, B.Sc, or M.Sc and 2–6 years of experience can apply.

2. Is sterile experience mandatory?

Yes, candidates must have experience in injectable or sterile pharmaceutical manufacturing.

3. What is the salary offered?

The salary ranges from β‚Ή3.5 LPA to β‚Ή7.5 LPA depending on experience and role.

4. How can I apply for this job?

You can apply by sending your updated resume to hr@erisbionxt.com.

5. What skills are required for this role?

Candidates should have knowledge of GMP, GLP, documentation, audits, and analytical testing.


Conclusion

If you have experience in sterile pharmaceutical environments and want to grow in quality operations, this opportunity at Eris Bionxt Private Limited is worth applying for. With strong exposure to regulatory practices and advanced manufacturing systems, this role can significantly boost your career in QA/QC. Don’t miss this chanceβ€”apply today.


Disclaimer

PharmaJobHub.in is an independent job information platform. We do not provide jobs or recruitment and are not affiliated with any company.


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