Psychotropics India Ltd. has announced a recruitment opportunity for experienced professionals in the Quality Control (QC) – HPLC department at its facility in Haridwar, Uttarakhand. Candidates with 4 to 5 years of relevant experience in HPLC analysis and pharmaceutical quality control can apply for this position.

This opportunity is suitable for pharmaceutical professionals with practical experience in handling HPLC instruments, analytical method execution, and routine quality control activities in accordance with Standard Operating Procedures (SOPs).

Job Overview

• Company Name: Psychotropics India Ltd.
• Department: Quality Control (QC) – HPLC
• Job Location: Haridwar, Uttarakhand
• Experience Required: 4 to 5 years
• Job Type: Pharmaceutical Industry
• Application Mode: Email
• Email ID: hrplant4@pilindia.in
• Contact Number: 7351010062

About Psychotropics India Ltd.

Psychotropics India Ltd. is a pharmaceutical company committed to better health. The company emphasizes quality-driven operations and professional development. This recruitment opportunity is intended for candidates with relevant analytical experience in pharmaceutical quality control.

Job Responsibilities

Selected candidates will be responsible for the following activities:

• Handling and operating HPLC instruments for pharmaceutical analysis.
• Performing routine quality control testing according to approved procedures.
• Executing analytical methods as per established protocols.
• Following Standard Operating Procedures (SOPs) and applicable laboratory practices.
• Supporting routine QC activities and maintaining accurate analytical records.
• Ensuring proper instrument operation and compliance with laboratory quality requirements.
• Assisting with documentation and reporting of analytical results.

Eligibility Criteria

Candidates applying for this position should have:

• 4 to 5 years of relevant experience in pharmaceutical Quality Control.
• Practical experience in HPLC operation and analysis.
• Knowledge of analytical method execution and routine laboratory procedures.
• Familiarity with SOPs and pharmaceutical quality control documentation.

The recruitment poster does not specify the required educational qualification, salary package, or application deadline. Candidates should confirm these details directly with the company before applying.

How to Apply

Interested and eligible candidates can apply by sending their updated CV to the official recruitment email address mentioned in the advertisement.

Email: hrplant4@pilindia.in

Contact Number: 7351010062

Location: Psychotropics India Ltd., Haridwar, Uttarakhand.

Candidates should mention “Application for QC – HPLC” in the email subject line and include their relevant work experience, technical skills, and contact information in their CV.

Before sharing personal documents, candidates should verify the recruitment details through the company.

Technical FAQs

1. What is HPLC in pharmaceutical Quality Control?

High-Performance Liquid Chromatography (HPLC) is an analytical technique used to separate, identify, and quantify components in pharmaceutical samples. It is widely used for assay testing, impurity profiling, and stability analysis of drug products.

2. What are the major components of an HPLC system?

The main components include the solvent reservoir, degasser, pump, sample injector or autosampler, analytical column, detector, and data acquisition system. Each component contributes to the separation, detection, and analysis of sample components.

3. What is the difference between HPLC assay and related substances testing?

An assay determines the amount or concentration of the active pharmaceutical ingredient (API) in a sample. Related substances testing evaluates impurities and degradation products present in the sample to help assess pharmaceutical quality and purity.

4. What are the important HPLC system suitability parameters?

Common system suitability parameters include retention time, peak area precision, resolution, theoretical plate count, and tailing factor. The applicable acceptance criteria depend on the approved analytical method and relevant pharmacopoeial or regulatory requirements.

5. What should a QC analyst check when an HPLC result fails acceptance criteria?

The analyst should review the chromatogram, sample preparation, standard preparation, mobile phase composition, instrument parameters, system suitability results, and relevant documentation. The issue should be investigated according to the laboratory’s approved procedure, with appropriate documentation and authorization before any repeat analysis.

Conclusion

Psychotropics India Ltd. offers a potential career opportunity for experienced pharmaceutical professionals in the QC – HPLC department at Haridwar. Candidates with 4 to 5 years of relevant HPLC and pharmaceutical quality control experience can submit their updated CV to hrplant4@pilindia.in or contact 7351010062 for further information.

Note: Vacancy availability and recruitment conditions should be confirmed directly with the company before applying.