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Indus Pharma Pvt. Ltd., a WHO-GMP Certified Sterile Injectable Manufacturing Company, is inviting applications from experienced pharmaceutical professionals for multiple vacancies across Purchase, Microbiology, Quality Control, Quality Assurance, Regulatory Affairs, and Production departments.
If you’re looking to advance your pharmaceutical career with a quality-driven organization, this is an excellent opportunity to join Indus Pharma’s state-of-the-art manufacturing facility in Neemrana, Rajasthan.
Company Details
- Company: Indus Pharma Pvt. Ltd.
- Industry: Pharmaceutical Manufacturing
- Facility: WHO-GMP Certified Sterile Injectable Manufacturing Facility
- Job Location: Neemrana, District Alwar, Rajasthan
- Employment Type: Full-Time
Current Openings
Purchase Department – Executive / Senior Executive
Experience Required: 5–6 Years
Job Responsibilities
- Procurement of Raw Materials (RM) and Packing Materials (PM)
- Vendor development, evaluation, and management
- Cost negotiation and timely material procurement
- Maintain purchase documentation and records
- Coordinate with QA, QC, Stores, and Production departments
Microbiology Department – Senior Executive
Experience Required: 5–6 Years
Job Responsibilities
- Perform sterility testing of pharmaceutical products
- Conduct environmental monitoring and trend analysis
- Media and reagent preparation
- Microbial identification and investigation
- Maintain laboratory documentation as per cGMP guidelines
Quality Control (QC) – Executive / Senior Executive
Experience Required: 7–8 Years
Job Responsibilities
- Operate and maintain HPLC systems
- Perform Analytical Method Validation (AMV)
- Conduct stability studies and prepare reports
- Analyze raw materials and finished products
- Ensure compliance with GLP, cGMP, and data integrity requirements
Quality Assurance (QA) – Senior Officer
Experience Required: 3–5 Years
Job Responsibilities
- Artwork review, approval, and change control
- Ensure compliance of packaging materials
- Review BMRs, BPRs, SOPs, and QA documentation
- Handle deviations, CAPA, and change control activities
- Support internal audits and regulatory inspections
Regulatory Affairs (RA) – Executive
Experience Required: 2–5 Years
Job Responsibilities
- Prepare CTD/eCTD dossiers
- Handle regulatory submissions to DCGI and State Authorities
- Compile technical and regulatory documentation
- Manage product registration and lifecycle activities
- Coordinate with regulatory agencies
Blister Operator
Experience Required: 2–4 Years
Job Responsibilities
- Operate blister packing machines
- Perform machine setup, line clearance, and format changes
- Carry out in-process quality checks
- Troubleshoot machine-related issues
- Follow cGMP, safety, and documentation practices
Eligibility Criteria
Candidates should possess:
- Relevant pharmaceutical industry experience in the applied department
- Good understanding of cGMP/GLP guidelines
- Strong documentation and compliance knowledge
- Good communication and teamwork skills
Job Location
Neemrana, District Alwar, Rajasthan
How to Apply
Interested candidates can send their updated resume mentioning the position applied for in the email subject line.
Email: hr@induspharmaindia.com
Contact Number: +91 99903 34200
Why Join Indus Pharma Pvt. Ltd.?
- WHO-GMP Certified Sterile Injectable Manufacturing Facility
- Opportunity to work with an experienced pharmaceutical team
- Professional and growth-oriented work environment
- Exposure to advanced pharmaceutical manufacturing practices
- Excellent career development opportunities
