NAARI has announced a Walk-In Interview Drive for experienced professionals in the pharmaceutical industry. The company is hiring for Production, Packing, Warehouse, and Engineering Projects departments for its Rudrapur, Uttarakhand manufacturing facility. Candidates with experience in USFDA/MHRA regulated plants and exposure to Hormones/Potent Molecules will be preferred.

If you are looking for a career opportunity in the pharma manufacturing sector, this recruitment drive offers multiple openings for operators, officers, executives, and managerial roles.

NAARI Recruitment – Overview

Particular Details

Company Name

NAARI

Job Type

Walk-In Interview

Work Location

Rudrapur, Uttarakhand

Walk-In Date

19th July 2026

Interview Time

9:30 AM to 5:30 PM

Interview Venue

Spice Hotel, Chakrata Road, Selakui Industrial Area, Dehradun, Uttarakhand

Industry

Pharmaceutical Manufacturing

Preferred Experience

USFDA/MHRA regulated plant, Hormones/Potent Molecules

Department-wise Vacancy Details

1. Production Department

Operator

Experience: 2–6 Years

Qualification: ITI / Diploma

Officer / Sr. Officer / Executive

Experience: 3–8 Years

Qualification: B.Pharm / M.Pharm

Required Skills

Compression

Coating

Granulation

Blending

BMR Documentation

Logbook Maintenance

ALCOA/ALCOA+

cGMP Compliance

SOP Compliance

QMS Activities

2. Packing Department

Blister (Primary & Secondary) Operator

Experience: 3–8 Years

Qualification: ITI / Diploma

Primary & Secondary Officer / Sr. Officer / Executive

Experience: 3–8 Years

Qualification: B.Pharm / M.Pharm

Required Skills

Blister Packing

Auto Cartoner

Serialization

Pouch Packing

Line Clearance

Dispensing

Changeovers

Calibration

Validation

Preventive Maintenance

CAPA

Change Control

Deviation Management

USFDA / EU-GMP / WHO Guidelines

3. Warehouse Department

Officer / Senior Officer

Experience: 2–8 Years

Qualification: B.Com / M.Com (Any Graduate)

Required Skills

AS/RS Warehouse Operations

GWP & GDP Compliance

ALCOA+

QMS

SOP Compliance

Real-Time Data Entry

Audit Readiness

Temperature & Usage Log Monitoring

Coordination with QA, QC, Production & Accounts

4. Engineering Projects

Sr. Executive / Assistant Manager / Deputy Manager

Experience: 10–15 Years

Qualification: B.E./B.Tech./M.E./M.Tech (Mechanical/Electrical/Civil)

Required Skills

Project Planning & Tracking

Deviation Reporting

Corrective Actions

Purchase Order Management

Delivery Coordination

Contractor Management

Documentation

Statutory Compliance

Audit Readiness

Team Coordination

Preferred Candidate Profile

Experience in USFDA/MHRA regulated pharmaceutical plants

Exposure to Hormones or Potent Molecule manufacturing

Strong understanding of cGMP, SOPs, QMS, ALCOA+, CAPA, Validation, and Documentation

Good communication and coordination skills

Documents Required

Candidates are requested to bring:

Updated Resume

Aadhaar Card

Salary Slips (Last 3 Months)

Educational Certificates

Experience Certificates

Recent Passport Size Photographs

Why Join NAARI?

Opportunity to work in a regulated pharmaceutical environment

Exposure to international quality standards

Career growth across multiple manufacturing functions

Professional work culture with advanced manufacturing practices

Technical FAQs

1. What regulatory experience is preferred for NAARI recruitment?

Candidates having experience in USFDA and MHRA regulated pharmaceutical manufacturing facilities will be given preference.

2. What is ALCOA+ in pharmaceutical documentation?

ALCOA+ stands for Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available, ensuring data integrity in pharma operations.

3. What is CAPA in pharmaceutical manufacturing?

CAPA (Corrective and Preventive Action) is a quality management process used to investigate deviations, eliminate root causes, and prevent recurrence of quality issues.

4. What is serialization in pharmaceutical packaging?

Serialization is the process of assigning a unique identification code to every medicine pack, enabling product traceability and helping prevent counterfeit drugs.

5. What is cGMP and why is it important?

Current Good Manufacturing Practices (cGMP) are regulatory standards that ensure medicines are consistently manufactured, tested, and controlled for quality, safety, and efficacy.