Unichem Laboratories Recruitment 2026
QC Officer & Senior Officer Vacancy
Unichem Laboratories Recruitment 2026: Unichem Laboratories is inviting applications for Quality Control positions at its pharmaceutical manufacturing facility in Ghaziabad, Uttar Pradesh. Candidates with pharmaceutical and analytical testing backgrounds can explore this career opportunity.
📋 Job Overview
Complete recruitment details – Unichem Laboratories
About Unichem Laboratories
Unichem Laboratories is an established pharmaceutical company engaged in the development and manufacturing of pharmaceutical products. The company operates in the pharmaceutical and life sciences sector, with a focus on pharmaceutical quality and manufacturing.
Working in a pharmaceutical Quality Control department provides professionals with opportunities to develop technical knowledge in analytical testing, instrumental analysis, laboratory operations, documentation and pharmaceutical quality systems.
The current recruitment for QC Officer and Senior Officer positions at Ghaziabad offers an opportunity for eligible pharmacy and life science graduates to explore roles involving HPLC analysis, analytical data processing, laboratory software and pharmaceutical sample testing.
🧪 Job Responsibilities
Key roles and responsibilities for QC Officer and Senior Officer at Unichem Laboratories.
1. HPLC Instrument Handling
- Handle and operate HPLC instruments for routine pharmaceutical analysis.
- Operate HPLC systems using Empower 3 software.
- Perform analytical testing of raw materials and finished products.
- Ensure proper instrument operation according to approved analytical procedures.
- Monitor chromatographic performance during analysis.
2. HPLC Calibration and Troubleshooting
- Perform calibration of HPLC instruments as per approved procedures.
- Independently handle day-to-day HPLC troubleshooting.
- Identify problems such as pressure fluctuations, baseline noise and peak splitting.
- Investigate chromatographic abnormalities.
- Maintain instrument calibration and troubleshooting records.
3. Empower 3 Software Handling
- Handle Empower 3 software for chromatographic data acquisition.
- Perform chromatographic integration and data processing.
- Review chromatograms and analytical results.
- Perform audit trail reviews in Empower software.
- Maintain electronic analytical records and data integrity.
4. TC Navigator Software Handling
- Handle TC Navigator software for analytical data management.
- Perform integration and analytical data processing.
- Review analytical data and associated records.
- Conduct audit trail reviews.
- Ensure accurate and traceable analytical documentation.
5. Pharmaceutical Sample Testing
- Perform testing of pharmaceutical raw materials.
- Carry out finished product and bulk finished product analysis.
- Perform analytical testing of stability samples.
- Handle Analytical Method Validation samples.
- Perform testing of Analytical Method Verification samples.
6. Analytical Method Validation & Verification
- Perform analytical testing as per approved validation protocols.
- Follow approved analytical procedures.
- Generate and document analytical results.
- Maintain validation and verification records.
7. Analytical Documentation & Reporting
- Report analytical test results in analytical worksheets.
- Maintain laboratory records as per Good Documentation Practices (GDP).
- Ensure accuracy and completeness of analytical records.
- Maintain traceable and properly documented laboratory data.
8. LIMS Handling
- Handle Laboratory Information Management System (LIMS).
- Enter and review analytical testing information.
- Maintain sample-related records and analytical results.
- Support laboratory workflow and electronic documentation.
🎯 Desired Skills & Requirements
Candidates should possess relevant pharmaceutical industry knowledge and practical analytical skills.
🌍 Preferred Regulatory Exposure
🎓 Educational Qualification
Candidates with the following educational qualifications can apply, subject to the employer’s eligibility criteria.
📘 Undergraduate Qualifications
📗 Postgraduate Qualifications
⏳ Required Work Experience
Experience in pharmaceutical Quality Control and analytical testing.
Candidates should have at least 60% overall academic marks, as mentioned in the job description.
📚 QC Interview Preparation Guide
Important technical topics candidates should revise before appearing for the Quality Control interview.
1. HPLC Fundamentals
Principle of HPLC, instrumentation, mobile phase, stationary phase, pumps, injectors, detectors, columns, chromatograms and system suitability.
2. HPLC Troubleshooting
High pressure, low pressure, baseline noise, peak tailing, peak fronting, peak splitting, retention time variation and ghost peaks.
3. Empower 3 Software
Data acquisition, chromatographic integration, processing methods, result review, audit trails and electronic data management.
4. TC Navigator Software
Software handling, analytical data processing, integration, result review and audit trail review.
5. HPLC Calibration
Calibration procedures and applicable performance checks for HPLC instruments, as per approved protocols and procedures.
6. Analytical Method Validation
Accuracy, precision, specificity, linearity, range, robustness, LOD and LOQ.
7. Pharmaceutical Analytical Testing
Assay, related substances, dissolution, content uniformity, raw material testing and finished product analysis.
8. Stability Testing
ICH stability guidelines, long-term studies, accelerated stability studies, stability chambers and stability sample analysis.
9. Good Documentation Practices (GDP)
Laboratory records, analytical worksheets, contemporaneous documentation, corrections, data traceability and documentation control.
10. Data Integrity – ALCOA+
Attributable, Legible, Contemporaneous, Original and Accurate, along with complete, consistent, enduring and available records.
11. LIMS
Laboratory Information Management System, sample tracking, result entry, sample status and electronic laboratory records.
12. Regulatory Compliance
Understanding of USFDA, MHRA, EU GMP, TGA requirements and pharmaceutical laboratory compliance.
Focus especially on HPLC troubleshooting, Empower 3 software, audit trail review, analytical method validation and data integrity. Prepare practical examples from your laboratory experience wherever applicable.
🚀 Why Should You Apply?
Explore the professional learning opportunities associated with pharmaceutical Quality Control roles.
Advanced Instrument Exposure
Develop practical knowledge of HPLC instruments and analytical testing.
Software Expertise
Gain exposure to Empower 3, TC Navigator and LIMS systems.
Analytical Skills
Strengthen knowledge of raw material, finished product and stability testing.
Regulatory Knowledge
Understand pharmaceutical documentation, data integrity and regulatory expectations.
Professional Development
Build technical expertise in pharmaceutical Quality Control and analytical operations.
Industry Experience
Explore laboratory operations and pharmaceutical quality systems.
📩 How to Apply?
Interested candidates should follow these steps to explore and apply for the advertised vacancy.
Check Your Eligibility
Review the educational qualifications, experience requirements and technical skills mentioned in the job description.
Prepare Your Updated Resume
Prepare your latest CV highlighting your HPLC experience, analytical testing skills, software knowledge and pharmaceutical industry experience.
Review the Recruitment Details
Visit the company’s recruitment listing to check the latest vacancy information and official application instructions.
View Unichem Laboratories Careers ↗Submit Your Application
Follow the application instructions provided in the recruitment listing. Ensure that all the information submitted is correct.
Candidates are advised to verify the current vacancy status and eligibility criteria before applying. Salary details have not been disclosed in the available job description.
❓ Frequently Asked Questions
Important questions about Unichem Laboratories Recruitment 2026.
1. Which positions are available at Unichem Laboratories?
The advertised positions are QC Officer and Senior Officer in the Quality Control department.
2. Where is the job location?
The job location is Meerut Road Industrial Area, Ghaziabad, Uttar Pradesh.
3. What is the required experience?
The advertised experience range is 0–5 years. Candidates should check the specific role requirements before applying.
4. What qualifications are required?
The listed undergraduate qualifications include B.Pharm and B.Sc. Postgraduate qualifications include M.Pharm, M.Sc. (Science), and MS. The job details also mention M.Sc. in Biochemistry.
5. Is HPLC knowledge required?
HPLC handling and analytical testing are among the key technical skills highlighted for these Quality Control positions.
6. Which software knowledge is useful?
Knowledge of Empower 3, TC Navigator and LIMS is relevant to the responsibilities described in the job information.
7. What is the salary for these positions?
Salary details have not been disclosed in the available job description. Candidates can confirm compensation during the recruitment process.
8. What is the minimum academic percentage?
The job details mention a minimum of 60% overall academic marks.
9. How can candidates apply?
Candidates should review the recruitment listing and follow the application instructions provided by the employer.
Pharmaacademias shares recruitment information for educational and career-awareness purposes. Candidates should verify the vacancy status and application process through the employer’s recruitment channel before submitting an application.
🚀 Interested in This Opportunity?
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Editorial Note
This article has been carefully researched and written by Deepak Rajput with a focus on accuracy, clarity, and evidence-based healthcare information. Pharmaacademias.com
