NAARI Walk-in R&D, QA, QC, Production

NAARI Walk-in R&D, QA, QC, Production

MSc MPharm ITI Jobs at NAARI Pharma Rudrapur | Walk-in

NAARI Pharma hiring R&D, QA, QC, Production professionals in Rudrapur. Multiple vacancies for MSc, M.Pharm, B.Pharm, ITI.

NAARI, a growing pharmaceutical organization known for its inclusive culture and regulated manufacturing standards, is conducting a walk-in interview to strengthen its R&D, Quality, and Production teams. This hiring drive is ideal for experienced professionals seeking long-term growth in a compliant, innovation-driven pharma environment supporting regulated markets.

Company Overview

NAARI is a professionally managed pharmaceutical company focused on quality-driven development and manufacturing of solid oral dosage forms. With a strong emphasis on regulatory compliance, process excellence, and people-first culture, NAARI continues to expand its operations across research, quality systems, and manufacturing. The organization actively supports GMP, GLP, and global regulatory expectations, making it a strong workplace for professionals aiming to build sustainable pharma careers.

Job Role & Responsibilities

Analytical R&D – Research Associate / Research Scientist

Experience: 3–8 Years
Qualification: M.Sc Chemistry

Key Responsibilities:

  • Analytical method development and validation for drug products
  • Analytical method transfer and cleaning validation activities
  • Preparation and review of protocols, reports, and SOPs
  • Ensuring compliance with GMP and GLP requirements
  • Supporting regulatory submissions and audits

Formulation R&D – Research Associate / Research Scientist

Experience: 3–8 Years
Qualification: M.Pharm (Pharmaceutics)

Key Responsibilities:

  • Formulation development of solid oral dosage forms for regulated markets
  • Process validation, scale-up, and troubleshooting activities
  • Lifecycle management of products to ensure long-term efficiency
  • MSAT support and technology transfer documentation
  • Collaboration with Analytical, QA, and Production teams

Quality Assurance – Executive

Experience: 4–6 Years
Qualification: M.Sc / M.Pharm

Key Responsibilities:

  • Oversight of GMP and GDP compliance across departments
  • Handling deviations, CAPA, change control, and investigations
  • Supporting internal and external regulatory audits
  • Ensuring compliance with SOPs and quality systems

Quality Control – Senior Officer / Executive

Experience: 3–6 Years
Qualification: M.Sc

Key Responsibilities:

  • Performing drug purity and dissolution testing
  • Analysis using UV/VIS, IR, and HPLC (Waters)
  • Stability studies and daily water analysis
  • Maintaining laboratory documentation as per cGMP

Production – Operator

Experience: 2–6 Years
Qualification: ITI / Diploma

Key Responsibilities:

  • Operation of compression, coating, granulation, and blending processes
  • Online BMR filling and documentation
  • Compliance with ALCOA and ALCOA+ principles
  • Adherence to cGMP and SOP requirements

Production – Senior Officer / Executive

Experience: 3–6 Years
Qualification: B.Pharm / M.Pharm

Key Responsibilities:

  • Supervising solid oral dosage manufacturing activities
  • Maintaining BMRs and equipment logbooks
  • Ensuring production activities meet cGMP norms
  • Supporting audits and validation activities

Eligibility / Qualifications

  • Educational background: M.Sc Chemistry, M.Pharm, B.Pharm, ITI, Diploma
  • Prior experience in regulated pharmaceutical manufacturing preferred
  • Exposure to USFDA and EU-GMP environments is an advantage

Relevant Courses

M.Sc Chemistry, M.Pharm Pharmaceutics, B.Pharm, Diploma in Pharmacy, ITI Mechanical / Production.

Location & Salary

Work Location: Rudrapur, Uttarakhand
Employment Type: Full-time

Salary will be offered as per industry standards and commensurate with experience and role.

Walk-in Interview Details

Date: 21st December 2025
Time: 9:30 AM – 5:30 PM

Venue: Hotel Le Mariet, Baddi–Nalagarh, Himachal Pradesh

Candidates unable to attend the walk-in may share their CV at ta@naari.co.

Application Process

  • Attend the walk-in interview with updated resume
  • Shortlisted candidates will be contacted for further rounds

FAQs

1. Is experience in regulated markets mandatory?
Preferred, especially USFDA and EU-GMP exposure, but not mandatory for all roles.

2. Can candidates from outside Uttarakhand apply?
Yes, candidates from any location may apply.

3. Are both R&D and Production roles available?
Yes, openings are available across R&D, Quality, and Production departments.

4. Is this a permanent position?
Yes, all roles are full-time permanent positions.

Summary Table

Company                                     NAARI Pharmaceuticals
Vacancies                                     Multiple – R&D, QA, QC, Production
Required Education                     M.Sc, M.Pharm, B.Pharm, ITI, Diploma
Experience                                   2–8 Years depending on role

NAARI Walk-in R&D, QA, QC, Production
NAARI Walk-in R&D, QA, QC, Production

To apply for this job email your details to ta@naari.co


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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