Gufic Biosciences Limited has announced recruitment opportunities for experienced professionals at its manufacturing facility in Navsari, Gujarat. The company is inviting applications for multiple positions in Production, Quality Assurance (QA), Quality Control (QC), QC Microbiology and QC Reviewer departments.

Candidates with relevant pharmaceutical qualifications and 3–10 years of experience can apply for these opportunities. Interested applicants should send their updated CV to the email address mentioned below.

Company Details

• Company Name: Gufic Biosciences Limited
• Job Location: Kabilpore, Navsari, Gujarat, India
• Job Type: Experienced Professionals
• Experience Required: 3–10 Years
• Positions: Officer / Senior Officer / Executive
• Industry: Pharmaceutical Manufacturing

1. Production Department

Qualification: B.Pharm / M.Pharm / M.Sc

Candidates should have relevant experience in pharmaceutical injectable manufacturing and production operations.

Key responsibilities and required experience include:

• Vial and ampoule filling
• Sealing and PFS operations
• Lyophilization injection
• Dry powder injection manufacturing
• Liquid injection manufacturing
• CIP/SIP operations

Candidates with experience in sterile injectable production and pharmaceutical manufacturing processes can apply.

2. Quality Assurance (QA) Department

Qualification: B.Pharm / M.Pharm / M.Sc

Candidates should have experience in quality assurance activities in an injectable manufacturing facility.

Key areas include:

• IPQA (In-Process Quality Assurance)
• Quality Management System (QMS)
• Change control
• Audit compliance
• Process validation
• Smoke studies
• Cleaning validation in injectable plants

Applicants with knowledge of GMP documentation, pharmaceutical quality systems and regulatory compliance will be suitable for these positions.

3. Quality Control – Microbiology Department

Qualification: M.Sc (Microbiology / Biotechnology)

Candidates should have relevant experience in microbiological testing and quality control activities in pharmaceutical manufacturing.

Key responsibilities include:

• Environmental monitoring
• Sterility testing
• Microbial Limit Test (MLT)
• Bacterial Endotoxin Test (BET)
• Media preparation

Experience in microbiological quality control and sterile pharmaceutical manufacturing will be beneficial.

4. Quality Control (QC) Department

Qualification: B.Sc / M.Sc / B.Pharm

Candidates with experience in pharmaceutical analytical testing and laboratory operations can apply.

Key responsibilities include:

• Analytical Method Validation (AMV)
• HPLC analysis
• Stability studies
• Raw material analysis
• Finished product analysis

Applicants should have relevant knowledge of analytical instruments, laboratory documentation and pharmaceutical quality control procedures.

5. Quality Control – Reviewer

Qualification: B.Sc / M.Sc / B.Pharm

Candidates should have experience in reviewing analytical data and pharmaceutical quality control documentation.

Key responsibilities include:

• Audit trail review
• Analytical data review
• Out-of-Specification (OOS) investigation and data review
• Out-of-Trend (OOT) investigation and data review

Candidates with knowledge of data integrity, laboratory compliance and analytical documentation will be suitable for this role.

How to Apply for Gufic Biosciences Recruitment 2026

Interested and eligible candidates should prepare their updated CV and send it to the recruitment email address provided in the official recruitment advertisement.

Email: binal.kapadia@guficbio.com

Contact Number: +91 63599 21281

Company Address: Gufic Biosciences Ltd., N.H. 48, Near GEB Grid, Kabilpore, Navsari – 396424, Gujarat, India.

Applicants should mention their preferred department and relevant experience in their application. Candidates are advised to verify the latest vacancy details before applying.

5 Technical FAQs – Gufic Biosciences Recruitment

1. What is the difference between vial filling and ampoule filling in pharmaceutical production?

Vial filling involves filling liquid or other suitable pharmaceutical preparations into vials, which are generally sealed with stoppers and caps. Ampoule filling involves filling the product into glass ampoules, which are hermetically sealed, typically by melting the glass neck.

2. What is IPQA, and why is it important in injectable manufacturing?

In-Process Quality Assurance (IPQA) monitors manufacturing activities to ensure compliance with approved procedures, GMP requirements and quality standards. It helps identify deviations and maintain consistent product quality during production.

3. What is the purpose of HPLC in pharmaceutical quality control?

High-Performance Liquid Chromatography (HPLC) is an analytical technique used to identify, separate and quantify components in pharmaceutical samples. It is commonly used for assay testing, impurity analysis and stability studies.

4. What is the difference between sterility testing, MLT and BET?

Sterility testing checks whether a pharmaceutical product is free from viable contaminating microorganisms. Microbial Limit Testing (MLT) evaluates microbial counts and specified microorganisms where applicable. Bacterial Endotoxin Testing (BET) detects bacterial endotoxins in products for which the test is required.

5. What are OOS, OOT and audit trail review in pharmaceutical QC?

Out-of-Specification (OOS) refers to a test result that falls outside established acceptance criteria. Out-of-Trend (OOT) refers to a result that deviates from expected historical or established trends. Audit trail review examines electronic records of actions and changes to help ensure data integrity and traceability.