Sentiss Pharma has announced a Walk-in Drive for experienced professionals in Production (Manufacturing & Filling), Quality Assurance, Quality Control, HR, and IT. Eligible candidates can attend the interview on 28 June 2026 at the specified venue in Paonta Sahib, Himachal Pradesh.
Sentiss Pharma is a leading ophthalmic, ENT, and inhalation pharmaceutical company with a strong global presence. The company is recognized as a Great Place to Work and continues to expand its manufacturing operations.
Company Overview
Sentiss Pharma specializes in ophthalmic, ENT, and inhalation pharmaceutical products and has operations across India, Russia, CIS, Europe, the USA, and other international markets. The company acquired Akorn AG in 2023, strengthening its global footprint and USFDA-compliant manufacturing capabilities.
Walk-in Interview Details
Company: Sentiss Pharma
Job Type: Walk-in Interview
Job Location: Nalagarh, Himachal Pradesh
Interview Date: 28 June 2026
Interview Time: 10:00 AM – 3:30 PM
Interview Venue: Hotel Grand Riviera, NH-72, Near Bata Bridge, Paonta Sahib (HP)
Departments, Qualification & Experience
1. Production (Manufacturing & Filling)
Operator
Qualification: ITI / Diploma
Experience: 3–7 Years
Skills:
Three-piece filling machine
Filter integrity testing
ORAB gloves integrity
Filtration vessels
LAF
Homogenizer
Area cleaning & sanitization
Documentation and machine qualification
Junior Executive
Qualification: B.Pharm / M.Pharm / M.Sc.
Experience: 2–5 Years
Skills:
Sterile manufacturing
Ophthalmic formulations
Autoclave operations
Batch manufacturing
GMP & Quality compliance
Executive
Qualification: B.Pharm / M.Pharm / M.Sc.
Experience: 4–8 Years
Skills:
Sterile filling operations
Autoclave handling
Ophthalmic manufacturing
Batch processing
GMP compliance
Senior Executive
Qualification: B.Pharm / M.Pharm / M.Sc.
Experience: 5–10 Years
Skills:
Sterile manufacturing
Filling operations
Autoclave operations
Quality systems
GMP standards
2. Quality Assurance
Junior Executive
Qualification: B.Pharm / M.Pharm / M.Sc.
Experience: 2–5 Years
Skills:
Equipment & Utility Validation
EM
IPQA
Aseptic manufacturing
Senior Executive
Qualification: B.Pharm / M.Pharm / M.Sc.
Experience: 5–10 Years
Skills:
Validation
Training
QMS
GLP (Lab Setup)
Aseptic manufacturing
3. Quality Control
Executive
Qualification: M.Sc. / M.Pharm / B.Pharm
Experience: 4–8 Years
Required Skills
Water validation
Risk assessment
IQ/OQ protocol readiness
Raw material sampling
Packing material testing
4. Human Resources (HR)
Executive / Senior Executive
Qualification: MBA (HR)
Experience: 5–10 Years
Experience in Talent Acquisition
Only female candidates with pharma experience are eligible.
5. Information Technology (IT)
Executive
Qualification: B.Tech (IT)
Experience: 4–8 Years
Skills
Validation methodologies
Infrastructure management
Automation
Networking
Equipment implementation
Documentation review
Documents to Carry
Updated Resume
Educational Certificates
Experience Certificates
Latest Salary Documents
Government ID Proof
Passport-size Photographs
Resume Submission
Candidates who are unable to attend the interview can send their updated resume to:
Email: planthr@sentisspharma.com
Subject Line: Designation – Department
Contact Number: 6230916292
Technical FAQs
1. What GMP knowledge is expected for Production roles?
Candidates should understand GMP requirements, sterile manufacturing practices, SOP compliance, documentation, batch manufacturing records, and contamination control.
2. What validation experience is required for QA positions?
QA candidates should have experience in Equipment & Utility Validation, EM monitoring, IPQA, QMS documentation, GLP, and aseptic process validation.
3. What technical skills are required in Quality Control?
QC professionals should have expertise in water validation, IQ/OQ protocols, risk assessment, raw material sampling, packing material testing, and laboratory documentation.
4. What equipment knowledge is important for Manufacturing & Filling roles?
Experience with three-piece filling machines, autoclaves, filtration systems, LAF units, homogenizers, filter integrity testing, and ORAB glove integrity testing is preferred.
5. What should candidates prepare before attending the interview?
Candidates should revise GMP, GDP, aseptic manufacturing, validation concepts, sterile operations, equipment qualification, documentation practices, and department-specific technical knowledge while carrying all required documents.


Leave a Comment