Job Description
M.Pharm, B.Pharm Injectable Jobs – Gufic Ahmedabad Walk-in
Gufic Biosciences walk-in interview Ahmedabad for QC, QA, Production Injectables. M.Pharm, B.Pharm, MSc eligible. 2–8 years exp.
Gufic Biosciences Limited is conducting a walk-in interview in Ahmedabad for experienced professionals across Quality Control, Quality Assurance, and Production departments in its injectable manufacturing division. This hiring drive targets skilled candidates who want to work in sterile injectable manufacturing within a globally recognized pharmaceutical organization.
This opportunity is highly relevant for professionals searching for injectable pharma jobs, sterile manufacturing roles, QC microbiology jobs, QA injectable positions, and production roles in regulated pharmaceutical plants. Gufic Biosciences offers exposure to advanced injectable technologies, strong quality systems, and long-term career stability in one of India’s leading injectable-focused pharma companies.
Immediate joiners with prior experience in sterile pharmaceutical plants will be given preference.
Company Overview
Gufic Biosciences Limited is a well-established Indian pharmaceutical company globally recognized as a major destination for injectable formulations. The company operates state-of-the-art sterile manufacturing facilities and follows stringent global regulatory standards across its operations.
With a strong portfolio of lyophilized injectables, liquid injectables, SVP and LVP products, Gufic Biosciences supplies to domestic and international markets. The organization is known for its robust quality culture, regulatory compliance, and continuous investment in advanced manufacturing technologies, making it a preferred employer for injectable professionals.
Job Role & Responsibilities
Quality Control – Chemical & Microbiology
QC professionals will be responsible for analytical and microbiological testing in compliance with pharmacopeial and regulatory standards.
Key responsibilities include:
• Analysis using HPLC, UPLC, GC, UV, and related instruments
• Chemical testing of raw materials, in-process samples, and finished products
• Microbiological testing including BET, sterility, MLT, media preparation, and environmental monitoring
• Maintaining analytical documentation and data integrity
• Supporting regulatory audits and inspections
Quality Assurance – Injectable
QA professionals will ensure compliance of injectable manufacturing operations with global quality and regulatory requirements.
Responsibilities include:
• In-process quality assurance (IPQA) activities in sterile areas
• Review of batch manufacturing and batch packing records
• Handling deviations, CAPA, change controls, and validations
• Ensuring compliance with GLP, QMS, and audit requirements
• Vendor qualification and regulatory documentation support
Production – Injectable
Production professionals will be involved in sterile injectable manufacturing operations.
Responsibilities include:
• Operating and monitoring aseptic manufacturing processes
• Handling SVP, LVP, and lyophilization operations
• Following sterile area practices and contamination control
• Maintaining production documentation
• Coordinating with QA and QC during manufacturing activities
These roles directly contribute to patient safety, product quality, and regulatory compliance in injectable pharmaceutical manufacturing.
Eligibility / Qualifications
Educational Qualification
M.Pharm, B.Pharm, M.Sc Chemistry, B.Sc Chemistry, M.Sc Microbiology, B.Sc Microbiology, M.Sc Biotechnology
