Rednex Pharmaceuticals Limited is hosting a Walk-In Interview from October 12 to 14, 2026, for various roles in Production, Quality Control, Quality Assurance, and Packing. The company seeks candidates with relevant experience in pharmaceutical formulation, welcoming both fresh graduates and seasoned professionals. Eligibility is restricted to candidates based in Gujarat. The available positions include roles such as Production QMS, Production Manager, Production Senior Officer, QC Reviewer, QC Officer, QA Officer, and Packing Officer, each requiring specific qualifications and experience levels. The interview will take place at the company’s location in Bavla, Ahmedabad, Gujarat, from 9:00 AM to 3:00 PM. Interested candidates can contact the company at +91 8799 692 591 during the specified hours or reach out via email at hr.rednex@gmail.com for further inquiries.
Vacancy details
1. Production QMS
- Qualification: B.Sc / M.Sc / B.Pharm
- Experience: 1–3 Years
- Openings: 02
- Job Description:
- Preparation of BPR, BMR, MPR & MFR
- Handling Quality Management System (QMS) activities in production
- Issuance of documents from QA
- Managing other production documentation activity
2. Production Manager
- Qualification: B.Sc./ M.Sc. / B.Pharm
- Experience: 5–7 Years
- Openings: 01
- Job Description:
- Tablets
- Capsules
- Oral Liquids
- External Preparations
3. Senior Officer – Production
- Qualification: B.Sc / M.Sc / B.Pharm
- Experience: 2–3 Years
- Openings: 02
- Job Description:
- Oral Liquid
- External Preparation
4. Reviewer – Quality Control
- Qualification: B.Sc. / M.Sc. / B.Pharm
- Experience: 5–7 Years
- Openings: 01
- Job Description:
- Review documents
- Dossier preparation
- Customer follow-up
- Respond to queries from customers
- Respond to regulatory authorities
5. Officer – Quality Control
- Qualification: M.Sc. / B.Pharm
- Experience: 0–1 Years
- Openings: 03
- Job Description:
- Documentation
- Chemical & Instrumental analysis including HPLC operations
6. Officer – Quality Assurance
- Qualification: M.Pharm
- Experience: 2 Years
- Openings: 02
- Job Description:
- ALL Master (Raw Material Master, Packing Material Master, Product Master, Formula Master) Handle
- Handling of Stability & Retain handling in Cloud Software
- Review of raw materials, Packing material, In-process & Finished-product Files.
7. Packing Officer
- Qualification: B.Sc. / M.Sc. / B.Pharm
- Experience: 2–3 Years
- Openings: 03
- Job Description:
- Responsible for managing and supervising the packaging process, Ensure compliance with GMP and SOPs
- Oversee the quality of finished products
Walk-in interview details
Date of interview: 12th – 14th October 2026
Interview Time: 9:00 AM – 3:00 PM
Interview Venue: Rednex Pharmaceuticals Limited, Survey No. 586 & 231, Near SKF Bearing, Bavla Bagodara NH-8A, Kerala, Ta. Bavla, Ahmedabad, Gujarat – 382220.
Contact +91 8799 692 591
Call Time 9:00 AM – 3:00 PM
Email: hr.rednex@gmail.com
Documents Required
- Updated Resume
- Increment Letter
- Last 3 months’ payslips from current organization
- Previous organization’s Relieving & Service Certificates
- All Educational Documents
- Aadhaar Card
Important Eligibility Note:
Only Gujarat-based candidates will be considered for the above position.
About Rednex Pharmaceuticals Pvt. Ltd.
Rednex Pharmaceuticals Pvt. Ltd. is a pharmaceutical enterprise established by experienced industry professionals and equipped with advanced technological infrastructure that adheres to WHO-GMP and PIC/S-GMP standards. The organization is committed to producing and supplying premium-quality pharmaceutical products, including Amoxicillin Capsules, Ampicillin Dicloxacillin Capsules, Cefixime Dicloxacillin Tablets, Cefixime Cloxacillin Tablets, Sultamicillin Tablets, and related formulations. Since its inception in 2017, the company has maintained a consistent focus on manufacturing excellence through the active involvement of its founding team. The organization operates a technologically advanced manufacturing facility situated in Ahmedabad, Gujarat, India, representing a substantial progression in pharmaceutical production capabilities. The facility incorporates state-of-the-art equipment and automation systems designed to reduce manual processes while maintaining rigorous standards across all operational divisions, including production, quality assurance, quality control, and research and development departments.