Tirupati Group Announces Multiple Career Opportunities at Paonta Sahib Facility

Tirupati Wellness Pvt. Ltd., a WHO-GMP certified pharmaceutical manufacturing organization under the Tirupati Group, has announced multiple openings for experienced professionals at its Paonta Sahib, Himachal Pradesh facility. The recruitment drive is focused on the EVT Tablet manufacturing division and offers opportunities across Production, Warehouse, Engineering, and Quality Assurance departments.

The company is seeking skilled candidates who are looking to build a long-term career in the pharmaceutical manufacturing sector. Positions are available from Operator level to Executive and Senior Officer roles, depending on department requirements and experience.

Available Departments and Open Positions

1. Production Department

Functions:

Granulation

Compression

Coating

Packing

Designation Level:

Operator to Executive

Production professionals will be responsible for manufacturing operations, equipment handling, batch processing, documentation, and compliance with GMP requirements.

2. Warehouse Department

Functions:

RM (Raw Material)

PM (Packing Material)

FG (Finished Goods)

Dispatch

Designation Level:

Officer to Senior Officer

Warehouse personnel will manage inventory control, material receipt, storage, dispensing, reconciliation, and dispatch activities while maintaining regulatory compliance.

3. Engineering Department

Functions:

HVAC

Fitter

Electrician

Water System

Designation Level:

Technician

Experience Required:

3–8 Years

Engineering professionals will ensure smooth operation and maintenance of manufacturing utilities, preventive maintenance programs, and equipment reliability.

4. Quality Assurance Department

Functions:

IPQA (In-Process Quality Assurance)

Qualification & Validation

Designation Level:

Senior Officer to Executive

Experience Required:

4–7 Years

QA professionals will oversee compliance activities, process validation, qualification protocols, batch review, investigations, and quality management systems.

Why Join Tirupati Wellness Pvt. Ltd.?

WHO-GMP Certified Manufacturing Facility

Growth-Oriented Work Environment

Opportunities Across Multiple Departments

Career Development and Learning Programs

Exposure to Modern Pharmaceutical Manufacturing Technologies

Professional and Compliance-Driven Culture

The company encourages talented professionals to become part of its growing pharmaceutical operations and contribute to maintaining high-quality manufacturing standards.

Contact Details

Contact Person: Vashu Kashyap

Designation: HR – Talent Acquisition

Company: Tirupati Wellness Pvt. Ltd.

Location: Paonta Sahib, Himachal Pradesh

Mobile: +91 78078 30308

Email: careers@tirupatigroup.co.in

Technical FAQs

1. What is a WHO-GMP certified pharmaceutical facility?

A WHO-GMP certified facility follows World Health Organization Good Manufacturing Practices to ensure medicines are consistently produced and controlled according to quality standards, safety requirements, and regulatory guidelines.

2. What are the key responsibilities in tablet production operations?

Tablet production professionals perform granulation, compression, coating, packing, equipment operation, batch documentation, line clearance, and adherence to GMP and safety procedures.

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

IPQA (In-Process Quality Assurance) monitors manufacturing activities in real time, verifies process compliance, checks documentation, and ensures product quality throughout production stages.

4. Why are HVAC and water systems important in pharmaceutical plants?

HVAC systems maintain temperature, humidity, and air cleanliness, while pharmaceutical water systems ensure purified water quality required for manufacturing and cleaning operations.

5. What is Qualification and Validation in the pharmaceutical industry?

Qualification and Validation are documented processes that confirm equipment, utilities, systems, and manufacturing processes consistently perform according to predefined specifications and regulatory requirements.