Ind Swift Laboratories Walk In for QA / QC Departments on 12th July 2026

A globally recognized pharmaceutical company, operating in over 85 countries, is hosting a walk-in drive to recruit experienced professionals for its Quality Assurance (QA) and Quality Control (QC) departments. The company is seeking skilled individuals to join its state-of-the-art manufacturing facility located in Derabassi, Punjab.

This recruitment drive targets candidates for Officer, Senior Officer, and Executive positions, offering a full-time career opportunity within the pharmaceutical industry.

Walk-in Interview Details:

  • Date: Sunday, July 12, 2026
  • Time: 9:00 AM – 6:00 PM
  • Interview Mode: Walk-in Interview
  • Work Location: Derabassi, Punjab

Interview Venue:
Redfox by Lemon Tree Hotels
Plot No. 1, Vasundhara Nagar, U.I.T.
Bhiwadi, Rajasthan – 301019

Educational Qualifications:
Applicants must hold one of the following degrees:

  • B.Pharm
  • M.Pharm
  • M.Sc. (Chemistry)

Department-wise Openings and Responsibilities:

Quality Assurance (QA)

  • Experience Required: 1–6 Years
  • Key Responsibilities: Professionals in QA will be involved in In-Process Quality Assurance (IPQA) activities, supporting validation processes, maintaining and implementing Quality Management System (QMS) procedures, ensuring compliance with Current Good Manufacturing Practices (cGMP), preparing and reviewing quality documentation, and contributing to regulatory compliance and quality improvement initiatives.

Quality Control (QC)

  • Experience Required: 1–8 Years
  • Key Responsibilities: QC professionals will perform analytical testing of various pharmaceutical samples and operate and maintain a range of analytical instruments. This includes proficiency with High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Particle Size Analyzers (PSA), UV Spectrophotometers, and Karl Fischer (KF) Titrators. Responsibilities also cover adhering to Good Manufacturing Practices (GMP) and laboratory procedures, maintaining meticulous laboratory documentation and analytical records, and ensuring compliance with all relevant quality standards and regulatory requirements.

Required Skills:

  • For QA: IPQA, Validation, QMS, cGMP Compliance, Documentation, Regulatory Compliance.
  • For QC: HPLC, Gas Chromatography (GC), Particle Size Analyzer (PSA), UV Spectrophotometer, Karl Fischer (KF), Laboratory Documentation, cGMP, Analytical Testing.

Preferred Candidate Profile:
The company values candidates with a strong background in pharmaceutical quality systems and excellent documentation and communication abilities. Preference will be given to professionals who have demonstrated experience in regulatory environments and have worked in regulated pharmaceutical manufacturing settings.

Documents to Carry for Interview:
Candidates attending the walk-in interview are requested to bring the following essential documents:

  • An updated Resume/CV
  • Original and photocopies of Educational Certificates
  • Experience Certificates from previous roles
  • Latest Salary Slips (if applicable)
  • A valid Government Photo ID Proof (such as Aadhaar, PAN, Passport, or Driving Licence)
  • Recent Passport-size Photographs

Why Join This Opportunity?
This is an excellent opportunity to build a robust career with a globally respected pharmaceutical leader. Employees gain exposure to advanced analytical instruments and comprehensive quality systems, while contributing to an organization known for its strong focus on innovation, quality, and compliance. The company is committed to employee development and offers significant career growth opportunities within both QA and QC functions.

Eligible candidates are encouraged to attend the walk-in interview on the specified date and time with all the required documents. Professionals with regulatory exposure will be given special consideration during the selection process.


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