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Naprod Life Sciences Walk-In Interview 2026 – Production, F&D, QA, Microbiology, EHS & Engineering Jobs in Boisar

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Exciting pharma jobs alert! Naprod Life Sciences is conducting walk-in interviews for freshers and experienced candidates in Production, F&D, QA, Microbiology, EHS, and Engineering roles at its EU GMP-approved injectable plant in Boisar, Maharashtra. Perfect opportunity for pharmaceutical careers in India.

About the Company

Naprod Life Sciences Pvt. Ltd. is a fast-growing Indian pharmaceutical company specializing in oncology (anti-cancer) and injectable formulations. The company operates a state-of-the-art EU GMP-approved manufacturing plant at MIDC Tarapur, Boisar, along with a dedicated Research and Development Centre at Dahisar.

It holds WHO cGMP approval, ISO 9001:2008 certification, and has recently secured ANVISA GMP renewal, demonstrating strong regulatory compliance. Naprod exports high-quality specialty products to around 30 countries, including regulated markets in Europe. As a pioneer in lyophilization and oncology injectables, the company focuses on innovation, advanced drug delivery systems, and excellence in manufacturing.

Job Details

  • Company Name: Naprod Life Sciences Pvt. Ltd.
  • Experience: 1 to 7 years (Experienced) / Freshers also eligible
  • Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc / Diploma / ITI / Any Graduates
  • Location: Plot No. G-17/1, MIDC, Boisar, Dist. Palghar, Maharashtra
  • Work Type: On-site

Job Description

Naprod Life Sciences is hiring multiple professionals for its EU GMP-approved injectable manufacturing plant in Boisar. The walk-in drive targets candidates from formulation and injectable plants for key departments including Production, Formulation & Development (F&D), Quality Assurance (QA), Microbiology, Environment Health & Safety (EHS), and Engineering.

These roles offer excellent opportunities in pharma production jobs, QA jobs, and related fields within a regulated, export-oriented environment.

Multiple Openings (Officer / Sr. Officer / Executive / Technician)

  • Department: Production / F&D / QA / Microbiology / EHS / Engineering
  • Market: Domestic + International (exports to ~30 countries)
  • Role: Officer / Sr. Officer / Executive / Technician
  • Experience: 1–7 years (Freshers welcome for select positions)
  • Education/Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc, Diploma, ITI, or Any Graduate

Skills/Qualifications

  • Relevant experience in sterile injectable or oncology formulation manufacturing (preferred)
  • Strong knowledge of cGMP, EU GMP, WHO GMP, and other regulatory standards
  • Hands-on experience in production, quality control/assurance, microbiology testing, or engineering maintenance
  • Ability to handle documentation, validation, and compliance processes
  • Team-oriented mindset with good communication and problem-solving skills
  • Freshers with relevant qualifications and eagerness to learn in a pharma environment

Key Responsibilities

  • Execute daily production activities as per SOPs and batch records
  • Perform quality assurance checks and documentation
  • Conduct microbiological testing and environmental monitoring
  • Ensure EHS compliance and safety protocols
  • Support formulation development and process optimization
  • Handle engineering maintenance and equipment qualification
  • Maintain regulatory records for audits and inspections

Benefits/Perks

  • Career growth in a rapidly expanding oncology-focused company
  • Exposure to international regulatory standards and global markets
  • Learning opportunities in advanced injectable and lyophilization technology
  • Competitive salary packages with performance-based increments
  • Professional work culture emphasizing innovation and compliance
  • Long-term stability in a WHO and EU GMP-approved facility

For more pharma job opportunities across India, explore listings on Pharma Recruiter.

How to Apply

Candidates meeting the eligibility criteria should attend the walk-in interview with all required documents.

Naprod Life Sciences Walk-In Interview 2026 – Production, F&D, QA, Microbiology, EHS & Engineering Jobs in Boisar

Documents Required:

  • Updated Resume
  • Last 3 Months Salary Slips
  • Increment & Appointment Letters
  • Original Qualification Certificates

Official Email: seema.patel@naprodgroup.com (for queries only)

Strong CTA: Don’t miss this chance to build your pharmaceutical career with a reputed oncology company. Prepare your documents and attend the walk-in drive!

Walk-in Interview Details

  • Date: 8th to 11th April 2026
  • Time: 10:00 AM – 4:00 PM
  • Venue: Plot No. G-17/1, MIDC, Boisar, Dist. Palghar, Maharashtra
  • Contact: 8421403723 / 7507846478
  • Email: seema.patel@naprodgroup.com

Why You Should Join

Joining Naprod Life Sciences means becoming part of a dynamic team committed to quality, innovation, and global healthcare. The company offers a supportive culture with recognition for performance, excellent learning platforms in cutting-edge oncology manufacturing, and long-term career stability in a compliant, growth-oriented environment.
With its strong regulatory track record and international presence, this is an ideal platform for professionals seeking pharma jobs in Maharashtra with global exposure.

FAQs

Q1: Who can apply for Naprod Life Sciences walk-in interview 2026?

A: Freshers and candidates with 1–7 years of experience in pharma production, QA, Microbiology, or related fields with relevant qualifications (B.Pharm, M.Pharm, B.Sc, etc.) can apply.

Q2: Is prior injectable or oncology experience mandatory?

A: Preferred for experienced roles, but freshers with suitable degrees are also encouraged, especially for entry-level positions in Production, QA, and Microbiology.

Q3: What documents are needed for the walk-in?

A: Bring your updated resume, last 3 months’ salary slips, increment/appointment letters, and original qualification certificates.

Q4: Are there growth opportunities at Naprod Life Sciences?

A: Yes. The company is expanding in regulated markets and offers clear career progression, skill development, and exposure to EU GMP and international standards.

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