India's DMPLOI - Jobs & Networking AppGufic Biosciences Limited, one of India’s leading pharmaceutical companies specializing in lyophilized injectables, has announced a Walk-In Interview Drive for Freshers at its Navsari, Gujarat facility. This recruitment initiative offers an excellent opportunity for recent graduates from pharmaceutical, microbiology, biotechnology, logistics, and HR backgrounds to begin their careers in a WHO-GMP and internationally accredited manufacturing environment.
The company is inviting enthusiastic and career-oriented candidates who graduated in 2024 or 2025 to join its growing workforce and contribute to the pharmaceutical industry’s evolving landscape.
About Gufic Biosciences
Established in 1970, Gufic Biosciences is recognized for its expertise in injectable formulations and lyophilization technology. The company operates manufacturing facilities that comply with global regulatory standards, including approvals from WHO-GMP, EU-GMP, Canada, Russia, and several international markets.
Working with Gufic provides exposure to advanced pharmaceutical manufacturing systems, quality standards, and regulatory practices.
Departments and Educational Qualifications
Microbiology (Male Candidates Only)
Qualification:
M.Sc. Microbiology
M.Sc. Biotechnology
B.Sc. Microbiology
Production (Injectable) / Quality Assurance (API) (Male Candidates Only)
Qualification:
M.Pharm
B.Pharm
M.Sc.
Store (Male Candidates Only)
Qualification:
M.A.
M.Com.
B.Sc.
MBA (Logistics & Supply Chain Management)
Human Resources (HR)
Qualification:
MBA (HR)
MHRD
PGHRD
Eligibility Criteria
Candidates must fulfill the following requirements:
Passed out in 2024 or 2025
Possess a valid degree certificate from a recognized university
Interested in building a career in the pharmaceutical industry
Ready to work in a professional manufacturing environment
Walk-In Interview Details
Date: 13 June 2026 (Saturday)
Time: 10:00 AM to 03:00 PM
Venue
Gufic Biosciences Ltd.
N.H. 48, Near GEB Grid,
Kabilpore, Navsari – 396424, Gujarat
Documents Required
Candidates should carry:
Updated Resume/CV
One Recent Passport Size Photograph
Educational Certificates
Identity Proof
Relevant Academic Documents
Contact Information
Email: binal.kapadia@guficbio.com
Mobile: +91 63599 21281
Why Join Gufic Biosciences?
Opportunity to work with a reputed pharmaceutical manufacturer
Exposure to injectable and lyophilization technologies
Learning environment for fresh graduates
Career growth in Production, QA, Microbiology, Stores, and HR
Experience with globally regulated manufacturing operations
Freshers seeking a strong foundation in the pharmaceutical industry should consider attending this walk-in drive and exploring the opportunities available at Gufic Biosciences.
Technical FAQs
1. What is lyophilization in injectable manufacturing?
Lyophilization, or freeze-drying, is a process used to remove water from pharmaceutical products under low temperature and vacuum conditions. It improves product stability, shelf life, and effectiveness, especially for sensitive injectable formulations.
2. What are the key responsibilities of a Quality Assurance (QA) professional in API manufacturing?
QA professionals ensure compliance with GMP guidelines, review batch manufacturing records, investigate deviations, monitor documentation practices, and maintain quality systems to ensure product safety and consistency.
3. Why is environmental monitoring important in pharmaceutical microbiology?
Environmental monitoring helps assess microbial contamination levels in cleanrooms and manufacturing areas. It ensures aseptic conditions are maintained and supports compliance with regulatory requirements.
4. What is the role of inventory management in pharmaceutical stores?
Inventory management ensures proper storage, receipt, dispensing, and tracking of raw materials, packaging materials, and finished products while maintaining traceability and regulatory compliance.
5. What are GMP guidelines and why are they important?
Good Manufacturing Practices (GMP) are regulations that ensure pharmaceutical products are consistently produced and controlled according to quality standards. GMP helps maintain product safety, efficacy, and regulatory compliance.
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