Gufic walk-in QC, QA, Production Injectables

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

Experience Requirement

• Quality Control (Chemical): 3 to 8 years with strong analytical instrument exposure
• Quality Control (Microbiology): 3 to 6 years with sterility and environmental monitoring experience
• Quality Assurance (Injectable): 2 to 6 years in sterile injectable QA and IPQA roles
• Production (Injectable): 3 to 5 years in aseptic manufacturing, SVP/LVP, and lyophilization

Preference will be given to candidates with prior experience in sterile pharmaceutical manufacturing plants.

Location & Salary

The work location is Ahmedabad, Gujarat. Salary will be competitive and aligned with industry standards for injectable manufacturing roles. Final compensation will depend on role, experience, and interview performance.

Walk-in Interview & Application Process

Walk-in Interview Details

Interview Venue:
Pinnacle Grand Hotel & Banquet,
Vrundavan Party Plot Road, Opposite Kargil Petrol Pump,
Near Doctor House, Sola, Ahmedabad – 380060, Gujarat

Date: 03 January 2026 (Saturday)
Time: 10:00 AM to 04:00 PM

Candidates are requested to carry the following documents:

• Updated resume
• Last 3 months salary slips
• Latest appointment letter
• Latest increment letter (if applicable)

Email Application Option

Candidates who are unable to attend the walk-in may share their resume to:

• binal.kapadia@guficbio.com

Immediate joiners will be given preference.

FAQs

Who can attend this walk-in interview?

Experienced professionals with relevant injectable, QC, QA, or production experience can attend.

Are freshers eligible?

No. These roles require prior experience in pharmaceutical manufacturing.

Is sterile injectable experience mandatory?

Yes. Preference is given to candidates with sterile plant exposure.

What designations are offered?

Officer, Senior Officer, and Executive positions based on experience.

Can I apply by email instead of walk-in?

Yes. You can email your resume if unable to attend the walk-in.

Summary Table

Company	Gufic Biosciences Limited
Vacancies	QC, QA & Production – Injectables
Required Education	M.Pharm, B.Pharm, M.Sc, B.Sc (Chemistry, Microbiology, Biotechnology)
Experience	2–8 Years (Sterile Injectables)