Cohance Life Sciences Limited has announced a walk-in recruitment drive for experienced professionals across Production, Quality Assurance, Quality Control, Analytical Quality Assurance, and Engineering departments. The hiring drive is aimed at strengthening its API and Formulation manufacturing operations located in Hyderabad, Telangana.

This recruitment initiative offers opportunities for candidates with pharmaceutical manufacturing, quality systems, analytical testing, and engineering backgrounds. Interested applicants meeting the eligibility criteria are encouraged to attend the walk-in interview with the required documents.

Company Overview

Cohance Life Sciences is a pharmaceutical organization engaged in the development and manufacturing of Active Pharmaceutical Ingredients (API) and Finished Dosage Formulations (FDF). The company focuses on quality-driven manufacturing practices, regulatory compliance, and advanced pharmaceutical technologies.

Walk-In Interview Details

Interview Date: 30 August 2026

Interview Time: 9:00 AM to 2:30 PM

Venue:

FDF Unit – I

Cohance Life Sciences Limited

A-19/CA-23A & A-23B, Road No. 18, IDA Nacharam, Uppal, Medchal-Malkajgiri, Telangana – 500076, India

Available Positions

1. Production – OSD

Experience: 2–10 Years

Qualification: B.Sc / Diploma

Designation: Operator / Executive

Location: Nacharam

Skill Requirements:

Pellet manufacturing

Glatt Fluid Bed Coater (FBC)

Pellet coating pan operations

OSD manufacturing processes

2. IPQA – OSD

Experience: 3–6 Years

Qualification: M.Sc / B.Pharm

Designation: Executive

Location: Nacharam

Skill Requirements:

Quality Management Systems (QMS)

Documentation practices

Regulatory compliance

In-process quality assurance activities

3. Quality Control – OSD

Experience: 3–6 Years

Qualification: M.Sc / B.Pharm

Designation: Executive

Location: Nacharam

Skill Requirements:

HPLC operation and troubleshooting

Gas Chromatography (GC)

UV Spectrophotometry

Analytical testing and documentation

4. API/OSD – Analytical Quality Assurance (AQA)

Experience: 3–8 Years

Qualification: M.Sc / B.Pharm

Designation: Executive

Location: Nacharam / Jaggaiapet

Skill Requirements:

Analytical data review

QC monitoring

Audit trail review

Data integrity compliance

Laboratory quality systems

5. Engineering & Maintenance – OSD

Experience: 3–5 Years

Qualification: Diploma / B.Tech

Designation: Engineer

Location: Pashamylaram

Skill Requirements:

Instrumentation systems

Equipment validation

Preventive maintenance

Calibration activities

Documents Required

Candidates should carry the following documents:

Updated Resume/CV

Photocopies of all Educational Certificates

Last Three Months’ Salary Slips

Current CTC Structure Details

Government Photo ID Proof

Experience Certificates (if available)

Why Join Cohance Life Sciences?

Exposure to regulated pharmaceutical manufacturing environments

Career growth in API and Formulation businesses

Opportunity to work with advanced analytical and production technologies

Strong focus on quality, compliance, and professional development

Collaborative work culture with experienced industry professionals

Technical FAQs

1. What is the role of HPLC in Quality Control laboratories?

High Performance Liquid Chromatography (HPLC) is one of the most important analytical techniques used in pharmaceutical QC laboratories. It helps determine assay, impurities, degradation products, and content uniformity of drug products. HPLC ensures that pharmaceutical products meet predefined quality standards before release.

2. Why is Audit Trail Review important in Analytical Quality Assurance?

Audit trail review is a critical data integrity requirement under global regulatory guidelines. It records every change made to electronic data, ensuring traceability, transparency, and compliance with regulations such as US FDA 21 CFR Part 11 and EU GMP requirements.

3. What are the key responsibilities of an IPQA professional in OSD manufacturing?

IPQA professionals monitor manufacturing activities in real time, verify process compliance, review batch records, conduct line clearance, ensure GMP adherence, and identify deviations during production to maintain product quality.

4. What is Fluid Bed Coating (FBC) used for in pellet manufacturing?

Fluid Bed Coating technology is used to apply functional coatings on pellets for controlled release, taste masking, moisture protection, and stability enhancement. It is widely utilized in Oral Solid Dosage (OSD) manufacturing.

5. What is equipment validation in pharmaceutical engineering?

Equipment validation is the documented process of demonstrating that manufacturing equipment consistently performs according to predetermined specifications. It includes IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) activities.

Conclusion

The Cohance Life Sciences Walk-In Drive 2026 presents an excellent opportunity for experienced pharmaceutical professionals seeking career growth in Production, Quality Assurance, Quality Control, Analytical Quality Assurance, and Engineering functions. Candidates possessing the required qualifications and experience should attend the interview with all necessary documents and take advantage of this opportunity to join a leading pharmaceutical organization.