Curefox Healthcare Pvt. Ltd., a rapidly growing pharmaceutical company committed to USFDA, WHO-GMP, and EU-GMP compliant manufacturing, has announced multiple job openings for its Injectable Small Volume Parenteral (SVP) Facility in Ahmedabad, Gujarat. The company is inviting applications from experienced professionals as well as freshers for Quality Control positions.

If you are looking for a career in the pharmaceutical manufacturing industry, this is an excellent opportunity to join a fast-growing organization offering career growth, transportation facilities, and a professional work environment.

Company Overview

Company Name: Curefox Healthcare Pvt. Ltd.

Curefox Healthcare specializes in pharmaceutical manufacturing with a strong focus on regulatory compliance and high-quality injectable products. The company is expanding its SVP Injectable Manufacturing Facility in Ahmedabad and is hiring talented professionals across Quality Control, Quality Assurance, Microbiology, and Engineering departments.

Job Details

Company: Curefox Healthcare Pvt. Ltd.

Industry: Pharmaceutical Manufacturing

Facility: Injectable Small Volume Parenteral (SVP)

Location: Ahmedabad, Gujarat

Employment Type: Full-Time

Application Mode: Email

Available Departments & Positions

Department

Designation

Qualification

Experience

Quality Control (QMS)

Executive / Sr. Executive

M.Sc., B.Pharm, M.Pharm

4–6 Years

Quality Control (AMV)

Executive / Sr. Executive

M.Sc., B.Pharm, M.Pharm

4–6 Years

Quality Control (Microbiology)

Officer / Executive

M.Sc.

2–5 Years

Quality Assurance

Officer / Executive

M.Sc., B.Pharm, M.Pharm

2–5 Years

Engineering

Officer

B.E. / Diploma

2–4 Years

Engineering

RO Operator

ITI / Diploma

2–4 Years

Freshers Opportunity

Curefox Healthcare has also invited freshers to apply for Quality Control (QC) positions.

This is a valuable opportunity for recent graduates looking to begin their careers in pharmaceutical manufacturing.

Required Qualifications

Applicants should possess one of the following qualifications depending on the position:

M.Sc.

B.Pharm

M.Pharm

B.E.

Diploma

ITI

Experience Required

Freshers: Eligible for Quality Control (QC) positions.

Experienced Candidates: 2 to 6 years, depending on the role.

Employee Benefits

Selected candidates will receive several benefits, including:

Transportation facility (Naroda, Bopal, Gota & Dholka)

Subsidized canteen

Growth-oriented work environment

Opportunity to work in a USFDA, WHO-GMP & EU-GMP compliant manufacturing facility

Career development in injectable pharmaceutical manufacturing

Job Location

Curefox Healthcare Pvt. Ltd.

Plot No. 86, Akshar Industrial Park,

Opposite Zydus Pharma, Sarkhej Bavla Road,

Vasna Chacharwadi,

Ahmedabad – 382213, Gujarat, India.

How to Apply

Interested candidates should send their updated CV to:

Email: hr@curefox.in

Applicants should mention the position applied for in the email subject line and ensure their resume includes updated educational qualifications, work experience, and contact details.

Why Join Curefox Healthcare?

Expanding Injectable SVP manufacturing facility

USFDA, WHO-GMP & EU-GMP compliant operations

Excellent learning opportunities

Career growth in pharmaceutical manufacturing

Freshers welcome for Quality Control positions

Employee-friendly work environment with transportation and canteen facilities

Technical FAQs

1. What is an SVP (Small Volume Parenteral) manufacturing facility?

SVP manufacturing facilities produce sterile injectable medicines generally packed in vials, ampoules, prefilled syringes, or small infusion containers. These facilities follow strict aseptic processing and regulatory standards.

2. What is the role of Quality Control (QMS and AMV) in pharmaceutical manufacturing?

Quality Control ensures raw materials, in-process samples, finished products, and stability samples meet predefined specifications. QMS focuses on quality systems and documentation, while AMV (Analytical Method Validation) verifies analytical methods for accuracy, precision, specificity, and robustness.

3. What are the responsibilities of a Quality Assurance Officer?

Quality Assurance professionals oversee GMP compliance, document review, deviation investigations, change control, CAPA implementation, internal audits, validation activities, and batch record approval to ensure consistent product quality.

4. What does a Microbiology Officer do in an injectable pharmaceutical plant?

Microbiology professionals perform environmental monitoring, water testing, sterility testing, microbial limit testing, media preparation, culture maintenance, and contamination control to ensure sterile manufacturing conditions.

5. What is the role of an RO Operator in a pharmaceutical facility?

An RO (Reverse Osmosis) Operator manages purified water systems by operating and monitoring RO equipment, conducting routine maintenance, recording operational parameters, and ensuring water quality complies with pharmaceutical standards for manufacturing.