Sentiss Pharma is hosting a walk-in interview for Quality Assurance (QA) and Production roles on Saturday, November 14, 2026, at its manufacturing facility in Nalagarh, Himachal Pradesh.
Event & Venue Details
- Date & Time. Saturday, November 14, 2026, from 10:00 AM to 4:00 PM.
- Venue. Sentiss Pharma Manufacturing Plant at Plant-Village Kehra Nihala, Tehsil Nalagarh, District Solan, Himachal Pradesh – 174101.
- Contact Numbers. 62309-16292 and 62309-16293.
Quality Assurance (QA)
- Executive – EM / Sr Executive – EM. Requires B.Pharma, M.Pharma, or M.Sc. with 4–8 years of experience in Environmental Monitoring (EM) in cleanroom areas, line clearance, in-process and bulk sampling, gowning qualification, nitrogen gas and compressed air sampling, SOPs, Change Controls (CC), Risk Assessments, and periodic HVAC/equipment qualification.
- Executive – IPQA / Sr Executive – IPQA. Requires B.Pharma, M.Pharma, or M.Sc. with 4–8 years of experience in line clearance, in-process and bulk sampling, IPQA activities, AQL inspection, QMS handling, SOP/investigation/risk assessment management, batch record review, and GMP-compliant HVAC/equipment qualification and validation.
- Executive – Validation. Requires B.Pharma, M.Pharma, or M.Sc. with 6–8 years of experience in QA Validation, including equipment qualification, process and cleaning validation, HVAC/utilities qualification, protocol and report review, risk assessment, change control, and GMP compliance.
Production
- Operator / Sr. Operator. Requires ITI or Diploma with 5–10 years of experience in CIP/SIP of manufacturing and holding tanks, filling machine operation, autoclave operation, homogenizer and bead mill operation, area cleaning, and aseptic manufacturing activities, including exposure to a Groninger three-piece filling machine.
- Jr Executive. Requires B.Pharma, M.Pharma, or M.Sc. with 2–5 years of experience in manufacturing suspension formulations, autoclave and CPZ operations, dispensing, filtration, sterilization, CIP/SIP, filter integrity testing, sanitization, and GMP compliance.
- Executive. Requires B.Pharma, M.Pharma, or M.Sc. with 5–8 years of experience in batch processing, sterilization, autoclave and CPZ operations, CIP/SIP, material dispensing, filter integrity testing, sanitization, and GMP compliance.
- Sr Executive. Requires B.Pharma, M.Pharma, or M.Sc. with 8–10 years of experience in shift operations, batch processing, sterilization, autoclave and CPZ activities, CIP/SIP, material dispensing, compliance management, sanitization, filter integrity testing, and QMS activities.
Candidate Requirements & How to Apply
Preferred Profile. Candidates should have experience in Ophthalmic formulations or a Sterile Injectable Plant, exposure to regulatory audits (USFDA, MHRA, EU GMP, WHO, TGA), and strong knowledge of GMP, compliance, quality systems, and documentation practices.
Walk-In Requirements. Bring an updated resume and your latest salary slip to the venue.
Email Option. You can also send your resume to planthr@sentisspharma.com using the subject line “Designation – Department”, or explore more openings on the Sentiss Pharma Careers Page
Are you planning to apply for a specific role here? If you share your current designation, qualification, and years of experience, I can help tailor your resume summary or draft an application email for the HR team.