Finecure Pharmaceuticals Limited, a leading pharmaceutical formulations manufacturer, has announced a Walk-In Interview for multiple positions across Manufacturing, Quality Control, Engineering, Warehouse, and Regulatory Affairs departments. The company manufactures Tablets, Capsules, and Dry Powder for Syrup and operates manufacturing facilities at Sanand/Changodar, Ahmedabad, Gujarat.

Candidates with relevant pharmaceutical (OSD) experience are invited to attend the interview on 05 July 2026 (Sunday).

About Finecure Pharmaceuticals Limited

Finecure Pharmaceuticals Limited is a well-established pharmaceutical company engaged in the manufacturing and marketing of high-quality pharmaceutical formulations. The company serves domestic and international markets while maintaining stringent quality standards. Its facilities are USFDA Audited, reflecting its commitment to global regulatory compliance and quality manufacturing.

Walk-In Interview Details

Company Name: Finecure Pharmaceuticals Limited

Interview Type: Walk-In Interview

Walk-In Date: 05 July 2026 (Sunday)

Reporting Time: 09:00 AM to 03:30 PM

Interview Venue: Finecure Pharmaceuticals Limited, A-1201, Mondeal Heights, Near Iskcon Circle, S.G. Highway, Ahmedabad, Gujarat

Departments, Qualifications & Vacancy Details

1. Manufacturing

Position 1

Department: Manufacturing

Experience: 1–4 Years

Qualification: B.Pharm / M.Pharm

Designation: Jr. Officer / Officer

Required Skills:

Primary Packing

Secondary Packing

QMS

Position 2

Department: Manufacturing

Experience: 2–6 Years

Qualification: B.Pharm / M.Pharm

Designation: Officer / Sr. Officer / Executive

Required Skills:

Production Chemist

2. Quality Control

Experience: 2–8 Years

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

Designation: Officer / Sr. Officer / Executive

Required Skills:

HPLC

Reviewer

Stability Studies

3. Engineering

Engineer Position

Experience: 1–3 Years

Qualification: B.E / B.Tech

Designation: Jr. Officer / Officer

Skills Required:

Plant Maintenance

HVAC

QMS

Electrical

Water System

Operator Position

Experience: 1–4 Years

Qualification: ITI / Diploma

Designation: Operator

Skills:

Water System

Electrical Maintenance

4. Warehouse

Experience: 2–8 Years

Qualification: B.Sc / M.Sc / B.Com

Designation: Officer / Sr. Officer / Executive / Sr. Executive

Skills Required:

RM Store

PM Store

Dispensing

Documentation

5. Regulatory Affairs

Experience: 2–5 Years

Qualification: B.Pharm / M.Pharm

Designation: Officer / Sr. Officer

Skills Required:

Dossier Preparation

ROW Market

US Market Documentation

Documents to Carry

Candidates should bring:

Updated Resume/CV

Recent Passport Size Photograph

Educational Certificates

Experience Certificates

Current Salary Documents (if applicable)

Government ID Proof

Latest Salary Slip

Why Join Finecure Pharmaceuticals?

USFDA Audited manufacturing environment

Career growth opportunities

Exposure to regulated markets

Modern OSD manufacturing facilities

Professional work culture

Learning opportunities across multiple pharmaceutical functions

Selection Process

Resume Screening

Technical Interview

HR Interview

Document Verification

Final Selection

Who Can Apply?

Candidates with relevant OSD pharmaceutical industry experience in Manufacturing, Quality Control, Engineering, Warehouse, or Regulatory Affairs who meet the qualification criteria are encouraged to attend the walk-in interview.

5 Technical FAQs

1. What is OSD manufacturing in the pharmaceutical industry?

OSD (Oral Solid Dosage) manufacturing involves the production of tablets, capsules, and similar oral dosage forms through processes such as granulation, compression, coating, capsule filling, and packaging under GMP guidelines.

2. Why is HPLC knowledge important for Quality Control?

High Performance Liquid Chromatography (HPLC) is used to identify, quantify, and verify the purity and potency of pharmaceutical products, making it one of the most essential analytical techniques in QC laboratories.

3. What does QMS mean in pharmaceutical manufacturing?

QMS (Quality Management System) is a structured framework that ensures pharmaceutical products are manufactured consistently according to GMP standards through documentation, deviation handling, CAPA, change control, and risk management.

4. What is the role of HVAC and Water Systems in pharmaceutical plants?

HVAC systems maintain controlled temperature, humidity, and air cleanliness to prevent contamination, while purified water systems supply water meeting pharmacopeial standards for manufacturing and cleaning processes.

5. What is dossier preparation in Regulatory Affairs?

Dossier preparation involves compiling technical and regulatory documents—including product quality, safety, efficacy, manufacturing, and stability data—for submission to health authorities in ROW (Rest of World) and regulated markets such as the US.