Ind-Swift Laboratories Limited has announced a Walk-In Drive 2026 for experienced pharmaceutical professionals in the Quality Assurance (QA) and Quality Control (QC) departments. Candidates with relevant educational qualifications and experience in pharmaceutical quality systems, analytical instruments, cGMP, and regulatory practices can attend the interview.

The recruitment drive is for the company’s Derabassi location, while the walk-in interview will be conducted in Bhiwadi, Rajasthan, on 12th July 2026.

Ind-Swift Laboratories Recruitment– Overview

Particulars Details

Company Name

Ind-Swift Laboratories Limited

Recruitment Type

Walk-In Drive

Departments

Quality Assurance & Quality Control

Positions

Officer / Senior Officer / Executive

Job Location

Derabassi

Qualifications

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

Experience

1–8 Years, depending on department

Walk-In Date

Sunday, 12th July 2026

Interview Time

9:00 AM to 6:00 PM

Interview Location

Red Fox by Lemon Tree Hotels, Bhiwadi, Rajasthan

Registration Mode

QR Code Registration / Walk-In Interview

About Ind-Swift Laboratories Limited

Ind-Swift Laboratories Limited is part of the Ind-Swift Group, which was founded in 1986 and is headquartered in Chandigarh, India.

The group operates in domestic and international pharmaceutical markets and has a presence in more than 85 countries. The company focuses on pharmaceutical innovation, quality, scientific advancement, healthcare excellence, and ethical business practices.

The latest recruitment drive offers an opportunity for experienced pharmaceutical professionals to build their careers in Quality Assurance and Quality Control functions.

Available Positions and Eligibility Criteria

Quality Assurance Department

Positions: Officer / Senior Officer / Executive

Qualification:

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

Experience Required:

1 to 6 years

Required Knowledge and Job Profile:

Candidates should have practical knowledge and experience in:

IPQA (In-Process Quality Assurance)

Validation activities

Quality Management Systems (QMS)

cGMP guidelines and compliance

Pharmaceutical quality systems

Documentation and quality procedures

Selected candidates will be responsible for ensuring compliance with cGMP guidelines and maintaining pharmaceutical quality standards.

Quality Control Department

Positions: Officer / Senior Officer / Executive

Qualification:

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

Experience Required:

1 to 8 years

Required Knowledge and Job Profile:

Candidates should have knowledge and hands-on experience in:

Finished Goods (FG) analysis

Raw Material (RM) testing

Packing Material (PM) testing

HPLC (High-Performance Liquid Chromatography)

GC (Gas Chromatography)

pH analysis

KF (Karl Fischer) analysis

cGMP guidelines and compliance

Candidates should have strong analytical skills and practical knowledge of pharmaceutical laboratory operations.

Important Note: Candidates with regulatory exposure will be preferred.

Walk-In Interview Details

The Ind-Swift Laboratories Walk-In Drive will be conducted as per the following schedule:

Walk-In Date: Sunday, 12th July 2026

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

Interview Venue:

Red Fox by Lemon Tree Hotels

Plot No. 1, Vasundhara Nagar,

U.I.T., Bhiwadi,

Rajasthan – 301019

How to Apply for Ind-Swift Laboratories Recruitment

Interested and eligible candidates can attend the walk-in interview at the scheduled venue. Candidates may also register by scanning the QR code provided in the official recruitment advertisement.

Applicants can forward their updated CVs to the official recruitment email addresses mentioned below:

Email: hr.gbu@indswiftlabs.com

Email: hrbp.gbu@indswiftlabs.com

Contact Numbers: 7087978441, 8219133802

Candidates should mention their relevant department, current experience, and position applied for while sending their CV.

Documents to Carry for the Walk-In Interview

Candidates are advised to carry an updated resume, passport-size photographs, educational certificates, experience certificates, current salary details, recent salary slips, identity proof, and other relevant professional documents.

Original documents may be required for verification during the recruitment process.

Important Instructions for Candidates

Candidates should carefully verify their eligibility criteria before attending the interview. Arriving early at the venue can help candidates complete registration and document verification smoothly.

Applicants should revise important technical topics related to their respective departments, including cGMP, QMS, validation, IPQA, HPLC, GC, data integrity, laboratory investigations, and pharmaceutical documentation practices.

Candidates with regulatory exposure should clearly highlight their relevant experience in their resumes and during the interview.

5 Technical FAQs for Ind-Swift Laboratories Interview

1. What is the difference between Quality Assurance and Quality Control in the pharmaceutical industry?

Answer: Quality Assurance is a system-oriented function focused on preventing quality problems by establishing procedures, systems, controls, and compliance processes. Quality Control is product-oriented and focuses on sampling, testing, analysis, and confirming that raw materials, in-process samples, and finished products meet predefined specifications.

2. What is IPQA, and what are the major responsibilities of an IPQA professional?

Answer: IPQA stands for In-Process Quality Assurance. Major responsibilities include line clearance, verification of manufacturing activities, review of batch records, in-process checks, environmental monitoring oversight, sampling, deviation reporting, and ensuring compliance with approved SOPs and cGMP requirements.

3. What is system suitability testing in HPLC?

Answer: System suitability testing is performed before or during sample analysis to confirm that the chromatographic system is capable of producing reliable and reproducible results. Common parameters include theoretical plates, tailing factor, resolution, retention time, and percentage relative standard deviation (%RSD).

4. What is the difference between deviation, CAPA, and change control?

Answer: A deviation is an unplanned departure from an approved procedure, specification, or established process. CAPA involves corrective actions to eliminate the cause of an existing problem and preventive actions to reduce the possibility of recurrence. Change control is a formal system used to evaluate, approve, implement, and document planned changes that may affect product quality or regulatory compliance.

5. What is data integrity in the pharmaceutical industry?

Answer: Data integrity refers to the completeness, consistency, accuracy, and reliability of data throughout its lifecycle. Pharmaceutical companies commonly follow the ALCOA+ principles, meaning data should be Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available.