India's DMPLOI - Jobs & Networking AppGUFIC Biosciences Limited has announced a Walk-In Interview for experienced pharmaceutical professionals and freshers at its injectable manufacturing facility in Navsari, Gujarat. The recruitment drive is scheduled for 11th July 2026 (Saturday).
The company is hiring candidates for Quality Assurance, Quality Control, Quality Control Microbiology, and Production (Injectable) departments. Candidates with qualifications such as M.Pharm, B.Pharm, M.Sc, and B.Sc and relevant pharmaceutical industry experience can attend the interview.
This recruitment drive offers opportunities ranging from Apprentice and Officer positions to Senior Officer, Executive, and Senior Executive roles.
GUFIC Biosciences Walk-In Interview Overview
Particulars Details
Company Name
GUFIC Biosciences Limited
Industry
Pharmaceutical / Injectable Manufacturing
Job Location
Navsari, Gujarat
Departments
Quality Assurance, Quality Control, QC Microbiology & Production
Designations
Apprentice, Officer, Sr. Officer, Executive & Sr. Executive
Qualifications
M.Pharm, B.Pharm, M.Sc & B.Sc
Experience Required
Freshers and candidates with 2–10 years of relevant experience, depending on the position
Walk-In Date
11th July 2026 (Saturday)
Interview Time
10:00 AM to 3:00 PM
Interview Mode
Walk-In Interview
About GUFIC Biosciences Limited
GUFIC Biosciences Limited is an established pharmaceutical company operating in the pharmaceutical industry since 1970. The company’s injectable manufacturing facility is located at Navsari, Gujarat.
According to the official recruitment advertisement, GUFIC has expertise in lyophilized injections and offers a wide range of API products. Its Navsari facility holds various international regulatory accreditations, including WHO GMP, EU GMP, Canada, Russia, Anvisa, Yemen, and Uzbekistan approvals, as stated in the recruitment notification.
Department-Wise Vacancy Details
1. Quality Assurance – Injectable
Qualification: M.Pharm / B.Pharm / M.Sc
Experience: 3 to 6 years
Designation: Officer / Senior Officer
Candidates should have experience working in an injectable manufacturing facility and knowledge of:
Validation of injection filling lines
Lyophilization equipment and processes
Autoclave operations
Dry Heat Sterilization (DHS)
Quality Management Systems (QMS)
2. Quality Control – Male Candidates Only
Qualification: M.Pharm / B.Pharm / M.Sc / B.Sc
Experience & Designation:
Candidates with 3 to 7 years of experience may be considered for Officer, Senior Officer, or Executive positions.
Applicants should have practical knowledge of analytical instruments, including:
HPLC
UPLC
Gas Chromatography (GC)
UV Spectrophotometer
Analytical Method Validation (AMV)
Candidates with 8 to 10 years of relevant experience and knowledge of HPLC and Analytical Method Validation may be considered for Executive or Senior Executive positions.
3. Quality Control Microbiology – Male Candidates Only
Qualification:
M.Sc (Microbiology/Biotechnology) or B.Sc (Microbiology/Biotechnology)
Experience: 2 to 6 years
Designation: Officer / Senior Officer
Candidates should possess knowledge and practical experience in:
Bacterial Endotoxin Test (BET)
Environmental Monitoring
Sterility Testing
Microbial Limit Test (MLT)
Culture handling
Media preparation
4. Production – Injectable (Male Candidates Only)
Qualification: M.Pharm / B.Pharm
Experience: 2 to 5 years
Designation: Officer / Senior Officer
Candidates should have experience in injectable manufacturing operations and knowledge of:
Injectable plant operations
Aseptic practices
Lyophilization
SVP/LVP manufacturing lines
PFS operations
Cartridge filling
Freshers can also attend the walk-in interview for Apprentice opportunities.
Walk-In Interview Date and Time
Date: 11th July 2026 (Saturday)
Time: 10:00 AM to 3:00 PM
Candidates are advised to reach the interview venue on time and carry all necessary documents.
Interview Venue
GUFIC Biosciences Limited
N.H. 48, Near GEB Grid,
Kabilpore, Navsari – 396424,
Gujarat.
Documents Required for the Interview
Interested candidates should carry:
Updated CV/Resume
One recent photograph
Educational certificates and mark sheets
Experience certificates, if applicable
Current salary slips and appointment letter, if available
Valid government-issued photo ID
How to Apply
Eligible candidates can directly attend the walk-in interview at the mentioned venue.
Candidates who are unable to attend or want to share their profiles can send their updated CV to:
Email: binal.kapadia@guficbio.com
Mobile Number: +91 63599 21281
Candidates should mention the department and position applied for in the email subject line for easier identification of their application.
Why Should Candidates Consider This Opportunity?
The GUFIC Biosciences recruitment drive provides opportunities for pharmaceutical professionals with experience in regulated injectable manufacturing environments.
Candidates with practical knowledge of GMP documentation, aseptic manufacturing, analytical instruments, microbiological testing, validation activities, QMS, and lyophilization technology may find relevant career opportunities through this recruitment drive.
Fresh B.Pharm and M.Pharm candidates interested in starting their careers in injectable pharmaceutical manufacturing can also attend for available Apprentice opportunities.
5 Technical FAQs for GUFIC Biosciences Walk-In Interview
1. What is lyophilization, and why is it used in injectable manufacturing?
Lyophilization, commonly known as freeze-drying, is a pharmaceutical manufacturing process used to remove water from temperature-sensitive products through freezing, primary drying (sublimation), and secondary drying (desorption).
It improves product stability, extends shelf life, and is commonly used for injectable products that are unstable in liquid formulations.
2. What is the difference between HPLC and UPLC?
HPLC (High-Performance Liquid Chromatography) uses conventional particle-size columns and operates at relatively lower pressures.
UPLC (Ultra-Performance Liquid Chromatography) generally uses smaller particle-size columns and higher operating pressures, which can provide faster analysis, improved resolution, and greater sensitivity.
Both techniques are widely used in pharmaceutical Quality Control laboratories for assay, impurity, dissolution, and stability testing.
3. What is Environmental Monitoring in an injectable manufacturing facility?
Environmental Monitoring is a systematic program used to evaluate the microbiological and particulate conditions of controlled manufacturing areas.
Common monitoring activities include active air sampling, passive air sampling using settle plates, surface monitoring, personnel monitoring, and non-viable particle monitoring.
The objective is to demonstrate that cleanrooms and aseptic manufacturing areas remain under a state of microbiological control.
4. What is the difference between Sterility Testing and the Bacterial Endotoxin Test (BET)?
Sterility Testing evaluates whether viable contaminating microorganisms are present in a pharmaceutical product.
BET detects or quantifies bacterial endotoxins, primarily lipopolysaccharides originating from Gram-negative bacteria.
A product can pass a sterility test but still contain unacceptable levels of bacterial endotoxins, so the tests serve different quality-control purposes.
5. What are the critical principles of aseptic practices in injectable production?
Critical aseptic practices include proper gowning, personnel hygiene, minimizing unnecessary interventions, maintaining first-air protection, correct material transfer procedures, regular disinfection, adherence to cleanroom behavior, and compliance with validated Standard Operating Procedures (SOPs).
Personnel working in aseptic areas should understand contamination-control principles and follow GMP requirements throughout manufacturing operations.
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