Sentiss Pharma, a globally recognized ophthalmic pharmaceutical company, has announced a Walk-In Drive on 21 June 2026 for experienced professionals across multiple departments. The company is known for its strong presence in ophthalmic, ENT, and inhalation segments and has consistently maintained high-quality manufacturing standards across international markets.

With a workforce of over 1,200 employees and recognition as a Great Place to Work, Sentiss Pharma offers excellent career opportunities for candidates looking to grow in sterile manufacturing, quality assurance, engineering, and validation functions.

Company Overview

Sentiss Pharma has established itself as one of the leading ophthalmic pharmaceutical companies with operations across India, Russia, CIS countries, Europe, the USA, and other international markets. The acquisition of Akorn AG has further strengthened its global footprint and manufacturing capabilities.

The company focuses on innovation, quality compliance, and continuous improvement while maintaining international regulatory standards.

Open Positions

Production (Manufacturing & Filling)

Operator

Qualification: ITI / Diploma

Experience: 3–7 Years

Jr. Executive

Qualification: B.Pharm / M.Pharm / M.Sc.

Experience: 2–5 Years

Executive

Qualification: B.Pharm / M.Pharm / M.Sc.

Experience: 4–8 Years

Sr. Executive

Qualification: B.Pharm / M.Pharm / M.Sc.

Experience: 5–10 Years

Quality Assurance

Jr. Executive

Qualification: B.Pharm / M.Pharm / M.Sc.

Experience: 2–5 Years

Sr. Executive

Qualification: B.Pharm / M.Pharm / M.Sc.

Experience: 5–10 Years

Quality Control

Executive

Qualification: M.Sc. / M.Pharm / B.Pharm

Experience: 4–8 Years

Engineering

Technician

Qualification: ITI / Diploma

Experience: 2–5 Years

Sr. Executive

Qualification: B.Tech (Mechanical)

Experience: 5–10 Years

EHS

ETP Operator

Qualification: ITI / Diploma

Experience: 2–5 Years

IT

Executive

Qualification: B.Tech (IT)

Experience: 4–8 Years

Walk-In Interview Details

Company: Sentiss Pharma

Date: 21 June 2026

Time: 10:00 AM – 4:00 PM

Venue: Hotel Le Mariet

Resume Submission

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

Email: planthr@sentisspharma.com

Subject Line: Designation – Department

Contact Number: 6230916292

Why Join Sentiss Pharma?

Global pharmaceutical organization

Strong focus on ophthalmic formulations

International regulatory exposure

Great Place to Work certified

Opportunities in sterile manufacturing and validation

Career growth in quality-driven environment

Technical FAQs

1. What is Filter Integrity Testing in sterile manufacturing?

Filter Integrity Testing verifies that sterilizing-grade filters are functioning properly and have not been damaged during processing. Common methods include Bubble Point, Diffusion, and Pressure Hold tests to ensure microbial retention capability.

2. What is ORAB glove integrity testing?

ORAB (Open Restricted Access Barrier) glove integrity testing ensures that gloves used in aseptic processing remain leak-free and maintain contamination control. Regular testing helps prevent microbial ingress into sterile manufacturing areas.

3. What is IQ/OQ/PQ in pharmaceutical validation?

IQ (Installation Qualification): Verifies equipment installation.

OQ (Operational Qualification): Confirms equipment operates as intended.

PQ (Performance Qualification): Demonstrates consistent performance under actual production conditions.

4. Why is HVAC critical in pharmaceutical manufacturing?

HVAC systems control temperature, humidity, pressure differentials, and airborne particles. Proper HVAC performance ensures GMP compliance and minimizes contamination risks in cleanroom environments.

5. What is Water System Validation in pharmaceutical facilities?

Water System Validation demonstrates that purified water and water-for-injection systems consistently produce water meeting predefined quality specifications. It includes monitoring microbial, chemical, and operational parameters.