PSA Chemicals & Pharmaceuticals Pvt. Ltd. has announced a Walk-In Interview Drive for experienced pharmaceutical professionals. The company is hiring candidates with 4–8 years of experience for multiple departments, including Quality Control (QC), Quality Assurance (QA), Analytical Method Validation (AMV), IPQA, and Stability Analysis. Candidates with hands-on expertise in HPLC, GC, UV-Visible Spectrophotometer, and FTIR/IR are encouraged to attend the interview.

About PSA Chemicals & Pharmaceuticals Pvt. Ltd.

PSA Chemicals & Pharmaceuticals Pvt. Ltd. is a fast-growing pharmaceutical organization serving international markets including ROW (Rest of the World), European Union (EU), and TGA-regulated countries. The company focuses on manufacturing affordable, high-quality medicines while maintaining compliance with global regulatory standards such as USFDA and EU GMP.

Job Details

Particular Details

Company Name

PSA Chemicals & Pharmaceuticals Pvt. Ltd.

Job Type

Walk-In Interview

Experience

4–8 Years

Departments

QC, QA, Analytical Method Validation, IPQA, Stability Analyst

Industry

Pharmaceutical

Interview Dates

01 August 2026 to 08 August 2026

Job Location

Pithampur, Madhya Pradesh

Open Positions

QC Analyst

QA Professional

Analytical Method Validation Expert

IPQA Professional

Stability Analyst

Required Experience

Candidates should possess 4–8 years of relevant pharmaceutical industry experience in:

Quality Control

Quality Assurance

Analytical Method Validation

In-Process Quality Assurance

Stability Studies

Instrument Knowledge Required

Applicants should have hands-on experience operating:

HPLC (High Performance Liquid Chromatography)

GC (Gas Chromatography)

UV-Visible Spectrophotometer

FTIR/IR (Fourier Transform Infrared Spectroscopy)

Mandatory Requirements

Candidates should have experience in:

HPLC, GC, UV-Visible and FTIR/IR operation

Analytical Method Validation as per ICH Guidelines

IPQA activities including line clearance, in-process checks and documentation review

Stability studies as per ICH Q1A guidelines

USFDA and EU GMP regulatory requirements

GMP Documentation

Data Integrity

Quality Management Systems (QMS)

Deviation Management

Why Join PSA?

Global exposure with ROW, EU and TGA markets

Opportunity to work with international regulatory standards

Innovation-driven work culture

Career growth opportunities

Patient-focused pharmaceutical manufacturing

Strong commitment to quality and compliance

Interview Details

Interview Dates: 01 August 2026 – 08 August 2026

Venue

PSA Chemicals & Pharmaceuticals Pvt. Ltd.

Plant – Indore SEZ,

Pithampur, Madhya Pradesh – 454775

Resume Submission

Candidates unable to attend the walk-in interview may send their updated resume to:

qc4.works@psachem.com

qc7.works@psachem.com

qa1.works@psachem.com

Contact Number: 9753793548

Documents to Carry

Candidates should bring:

Updated Resume

Educational Certificates

Experience Certificates

Latest Salary Slip/CTC Details

Government Photo ID

Passport-size Photographs

Selection Process

Walk-In Registration

HR Screening

Technical Interview

Department Discussion

Final HR Round

Offer for Selected Candidates

Technical FAQs

1. What is Analytical Method Validation (AMV)?

Analytical Method Validation is the process of demonstrating that an analytical method consistently produces reliable, accurate, precise and reproducible results according to ICH Q2(R2) guidelines.

2. Why is HPLC widely used in pharmaceutical quality control?

HPLC is used to identify, separate and quantify pharmaceutical compounds, impurities and degradation products with high accuracy and precision.

3. What is the role of IPQA in pharmaceutical manufacturing?

IPQA monitors manufacturing activities through line clearance, in-process checks, documentation review, sampling and GMP compliance to ensure consistent product quality.

4. What are Stability Studies according to ICH Q1A?

Stability studies evaluate how a drug product maintains its quality, safety and efficacy under different environmental conditions to establish shelf life and storage requirements.

5. Why are USFDA and EU GMP regulations important?

Compliance with USFDA and EU GMP ensures pharmaceutical products are manufactured under internationally accepted quality standards, enabling approval for regulated global markets.

Conclusion

The PSA Chemicals & Pharmaceuticals Walk-In Interview offers an excellent opportunity for experienced pharma professionals specializing in QC, QA, AMV, IPQA, and Stability Analysis. Candidates with expertise in analytical instruments, GMP documentation, regulatory compliance, and quality systems should take advantage of this recruitment drive and attend the interview with all required documents.