Ind-Swift Laboratories Limited has announced a Walk-In Drive 2026 for experienced pharmaceutical professionals at its Derabassi location. The company is hiring candidates for multiple positions in the Quality Control, Packing, and Production departments.

Candidates with qualifications such as B.Pharm, M.Pharm, M.Sc Chemistry, 10+2, and ITI, along with relevant pharmaceutical industry experience, can participate in this recruitment drive.

The walk-in interview is scheduled for 19th July 2026 at Baddi, Himachal Pradesh. Interested candidates should carefully review the eligibility criteria, technical requirements, and interview details before attending.

Ind-Swift Laboratories Recruitment – Overview

Particulars Details

Company Name

Ind-Swift Laboratories Limited

Job Location

Derabassi

Departments

Quality Control, Packing & Production

Positions

Officer, Sr. Officer, Executive, Operator & Sr. Operator

Qualifications

B.Pharm, M.Pharm, M.Sc Chemistry, 10+2 or ITI

Experience Required

1 to 8 Years, depending on position

Walk-In Date

Sunday, 19th July 2026

Interview Time

9:00 AM to 6:00 PM

Walk-In Location

Lemon Tree Hotel, Baddi, Himachal Pradesh

Industry

Pharmaceutical Industry

About Ind-Swift Laboratories Limited

Ind-Swift Group was founded in 1986 and is headquartered in Chandigarh, India. The company is a globally recognized pharmaceutical organization with a presence in more than 85 countries.

Ind-Swift Laboratories focuses on scientific advancement, innovation, pharmaceutical quality, and ethical business practices. The organization operates in both domestic and export pharmaceutical markets.

This recruitment drive offers experienced pharmaceutical professionals an opportunity to work in Quality Control, Packing, and Production operations.

Ind-Swift Laboratories Vacancy Details

Quality Control Department

Position: Officer / Senior Officer / Executive

Qualification:

B.Pharm / M.Pharm / M.Sc Chemistry

Experience Required: 1 to 8 Years

Technical Profile & Responsibilities:

Candidates should have practical knowledge of Finished Goods (FG), Raw Materials (RM), and Packing Materials (PM) testing and documentation.

Applicants should understand laboratory procedures and pharmaceutical quality systems and be responsible for adherence to current Good Manufacturing Practices (cGMP) guidelines.

Packing Department

Position: Officer / Senior Officer

Qualification: B.Pharm

Experience Required: 1 to 8 Years

Technical Profile & Responsibilities:

Candidates should have supervisory experience in pharmaceutical packing operations.

Applicants should possess knowledge of:

Pharmaceutical packing operations

Batch Operating System (BOS)

Auto-cartonator machines

Packing line supervision

cGMP compliance and documentation

Candidates will be responsible for ensuring that packing activities are performed according to approved procedures and cGMP requirements.

Production Department – Officer / Senior Officer / Executive

Qualification: B.Pharm

Experience Required: 2 to 7 Years

Technical Profile & Responsibilities:

Candidates should have practical knowledge of pharmaceutical manufacturing operations, including:

Granulation

Compression

Capsule Filling

Selected professionals will be responsible for manufacturing activities and adherence to applicable cGMP guidelines.

Production Department – Operator / Senior Operator

Qualification: 10+2 or ITI

Experience Required: 1 to 7 Years

Technical Profile & Responsibilities:

Candidates should have hands-on experience in pharmaceutical manufacturing operations, including:

Compression

Granulation

Coating

Applicants should understand equipment operation, manufacturing procedures, safety requirements, and cGMP practices.

Note: Candidates having regulatory exposure will be preferred.

Walk-In Interview Details

Walk-In Date: Sunday, 19th July 2026

Interview Time: 9:00 AM to 6:00 PM

Interview Venue:

Lemon Tree Hotel

NH 21A, Baddi-Nalagarh Highway,

Bhud, Solan District,

Baddi, Himachal Pradesh

How to Apply for Ind-Swift Laboratories Recruitment

Eligible candidates can attend the walk-in interview directly at the mentioned venue on 19th July 2026.

Candidates may also forward their updated CVs to the recruitment contacts provided by the company.

Email Addresses:

hr.gbu@indswiftlabs.com

hrbp.rd@indswiftlabs.com

Contact Numbers:

8219133802

8894599858

Candidates can also use the QR code provided in the official recruitment advertisement to register for the recruitment drive.

Documents to Carry for the Walk-In Interview

Candidates are advised to carry an updated resume/CV, recent passport-size photographs, educational certificates, experience certificates, salary slips or current CTC proof, Aadhaar Card or another valid government-issued photo ID, and copies of relevant pharmaceutical training or technical certificates.

Important Instructions for Candidates

Candidates should verify that their qualifications and professional experience match the requirements of the position before attending.

Arrive at the interview venue on time and carry all relevant documents. Candidates working in pharmaceutical manufacturing should be prepared to answer questions related to cGMP, SOPs, GDP, data integrity, deviation handling, equipment operations, documentation, and regulatory compliance.

Regulatory exposure may provide an advantage during the selection process.

5 Technical FAQs for Ind-Swift Laboratories Walk-In Interview

1. What is the difference between Raw Material, Packing Material, and Finished Goods testing in Quality Control?

Answer: Raw Material testing verifies the identity, purity, potency, and quality of materials before they are released for manufacturing. Packing Material testing evaluates packaging components such as bottles, foils, cartons, and labels against approved specifications. Finished Goods testing confirms that the manufactured product complies with approved specifications before batch release.

2. What is cGMP, and why is it important in pharmaceutical manufacturing?

Answer: cGMP stands for current Good Manufacturing Practices. It is a regulatory framework that ensures pharmaceutical products are consistently manufactured, tested, documented, and controlled according to established quality standards. Compliance with cGMP helps prevent contamination, mix-ups, documentation errors, and product quality failures.

3. What are the critical parameters monitored during tablet compression?

Answer: Important parameters include tablet weight, hardness, thickness, friability, disintegration time, compression force, machine speed, appearance, and metal detection. Operators and production officers must monitor these parameters according to the Batch Manufacturing Record and approved SOPs.

4. What is the purpose of granulation in pharmaceutical manufacturing?

Answer: Granulation improves the flow properties, compressibility, content uniformity, and handling characteristics of powder mixtures. Wet granulation and dry granulation are commonly used methods. Critical process parameters must be controlled to achieve consistent granule quality and final product performance.

5. What is line clearance in pharmaceutical production and packing areas?

Answer: Line clearance is a documented procedure performed before starting manufacturing or packing operations. It ensures that materials, documents, labels, products, and residues from previous batches have been removed from the area. Proper line clearance helps prevent product mix-ups, cross-contamination, and labeling errors.

Conclusion

The Ind-Swift Laboratories Walk-In Drive 2026 is an excellent opportunity for experienced candidates seeking pharmaceutical jobs in Quality Control, Packing, and Production departments.

Eligible candidates with 1 to 8 years of relevant experience can attend the walk-in interview on 19th July 2026 at Lemon Tree Hotel, Baddi, Himachal Pradesh.

Candidates are advised to review the job requirements, prepare relevant technical interview topics, carry all necessary documents, and verify the recruitment information from the official advertisement before attending.