Ind-Swift Laboratories Limited, a globally trusted pharmaceutical company with operations in more than 85 countries, is conducting a Walk-in Drive for experienced professionals in Quality Assurance (QA) and Quality Control (QC). The company is looking for talented candidates with experience in pharmaceutical quality systems, regulatory compliance, and analytical testing to join its Derabassi manufacturing facility.
🌟 Walk-in Drive Highlights
| Particulars | Details |
|---|---|
| Company Name | Ind-Swift Laboratories Limited |
| Industry | Pharmaceutical |
| Departments | Quality Assurance (QA) & Quality Control (QC) |
| Job Type | Full-Time |
| Positions | Officer / Sr. Officer / Executive |
| Experience Required | 1–8 Years |
| Interview Date | 12 July 2026 (Sunday) |
| Interview Time | 9:00 AM – 6:00 PM |
| Work Location | Derabassi, Punjab |
| Interview Mode | Walk-in Interview |
📢 Department-wise Openings
| Department | Position | Qualification | Experience |
|---|---|---|---|
| Quality Assurance (QA) | Officer / Sr. Officer / Executive | B.Pharm / M.Pharm / M.Sc. (Chemistry) | 1–6 Years |
| Quality Control (QC) | Officer / Sr. Officer / Executive | B.Pharm / M.Pharm / M.Sc. (Chemistry) | 1–8 Years |
🎓 Educational Qualification
Candidates should possess any one of the following qualifications:
- B.Pharm
- M.Pharm
- M.Sc. (Chemistry)
💼 Job Responsibilities
🧪 Quality Assurance (QA)
Experience: 1–6 Years
Key Responsibilities
- Handle IPQA (In-Process Quality Assurance) activities.
- Support Validation activities.
- Maintain and implement Quality Management System (QMS) procedures.
- Ensure compliance with Current Good Manufacturing Practices (cGMP).
- Prepare and review quality documentation.
- Support regulatory compliance and quality improvement initiatives.
🔬 Quality Control (QC)
Experience: 1–8 Years
Key Responsibilities
- Perform analytical testing of pharmaceutical samples.
- Operate and maintain analytical instruments including:
- HPLC
- Gas Chromatography (GC)
- Particle Size Analyzer (PSA)
- UV Spectrophotometer
- Karl Fischer (KF) Titrator
- Follow Good Manufacturing Practices (GMP) and laboratory procedures.
- Maintain laboratory documentation and analytical records.
- Ensure compliance with quality standards and regulatory requirements.
🎯 Required Skills
Quality Assurance
- IPQA
- Validation
- Quality Management System (QMS)
- cGMP Compliance
- Documentation
- Regulatory Compliance
Quality Control
- HPLC
- Gas Chromatography (GC)
- Particle Size Analyzer (PSA)
- UV Spectrophotometer
- Karl Fischer (KF)
- Laboratory Documentation
- cGMP
- Analytical Testing
⭐ Preferred Candidate Profile
- Candidates with regulatory exposure will be given preference.
- Strong knowledge of pharmaceutical quality systems.
- Good documentation and communication skills.
- Experience working in regulated pharmaceutical manufacturing environments.
📅 Walk-in Interview Schedule
| Event | Details |
|---|---|
| Interview Date | 12 July 2026 (Sunday) |
| Interview Time | 9:00 AM – 6:00 PM |
📍 Interview Venue
Redfox by Lemon Tree Hotels
Plot No. 1
Vasundhara Nagar
U.I.T., Bhiwadi
Rajasthan – 301019
📍 Work Location
Ind-Swift Laboratories Limited
NH-21, Village Jawaharpur
Derabassi
District SAS Nagar (Mohali)
Punjab – 140507
📄 Documents to Carry
Candidates should bring:
- Updated Resume/CV
- Educational Certificates (Original & Photocopies)
- Experience Certificates
- Latest Salary Slips (if applicable)
- Government Photo ID Proof (Aadhaar/PAN/Passport/Driving Licence)
- Recent Passport-size Photographs
📧 Email IDs
Interested candidates may also forward their updated resumes to:
📞 Contact Numbers
- 7087978441
- 8219133802
✅ Who Can Apply?
- B.Pharm, M.Pharm, and M.Sc. (Chemistry) graduates.
- Professionals with 1–8 years of experience in Quality Assurance or Quality Control.
- Candidates with experience in IPQA, Validation, QMS, HPLC, GC, PSA, UV, or Karl Fischer.
- Professionals with regulatory exposure are preferred.
⭐ Why Join Ind-Swift Laboratories?
- Work with a globally recognized pharmaceutical company operating in 85+ countries.
- Opportunity to build a career in a regulated pharmaceutical manufacturing environment.
- Exposure to advanced analytical instruments and quality systems.
- Strong focus on innovation, quality, compliance, and employee development.
- Career growth opportunities in QA and QC functions.
📢 Important Note
Eligible candidates are requested to attend the walk-in interview on 12 July 2026 between 9:00 AM and 6:00 PM with all required documents. Candidates who are unable to attend may send their updated resumes to the official email IDs provided above. Professionals with regulatory exposure will be given preference during the selection process.
