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Apnar Pharma Walk-in Interview on 12 April 2026 | Vacancies in Production, QA, QC & Validation in Vadodara

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Explore exciting pharma jobs at Apnar Pharma, a subsidiary of Senores Pharmaceuticals. This walk-in interview on 12 April 2026 offers multiple openings in Production, Packaging, Quality Control (QC), Quality Assurance (QA), Microbiology, and Central Validation Lab. Ideal for professionals seeking pharmaceutical careers in India with USFDA-compliant manufacturing experience.

About the Company

Senores Pharmaceuticals is a rapidly growing, thought-leading global pharmaceutical company committed to innovation, quality, and global wellness. Through its subsidiary Apnar Pharma Private Limited, the company operates a modern, USFDA, UK-MHRA, and Health Canada-approved manufacturing facility in Vadodara, Gujarat.

Apnar Pharma specializes in the development and manufacturing of high-quality generic formulations for regulated markets including the US, UK, and Canada. The recent acquisition strengthens Senores’ manufacturing capabilities, adds valuable ANDAs, and supports expanded capacity for complex generics and international supply.

Job Details

  • Company Name: Apnar Pharma Private Limited (A Subsidiary of Senores Pharmaceuticals Limited)
  • Experience: Varies by role (3–12 years)
  • Qualification: B.Pharm, M.Pharm, M.Sc, B.Sc, M.Sc (Microbiology)
  • Location: Apnar Pharma Plant, Block No. 102, At & Post Gavasad, Padra Jambusar Road, Taluka Padra, District Vadodara-391430, Gujarat
  • Work Type: On-site

Job Description

Apnar Pharma is actively hiring experienced professionals for various roles across production, packaging, quality control, quality assurance, microbiology, and validation departments. These positions focus on USFDA compliance, advanced manufacturing processes, and quality systems in a state-of-the-art facility.

Assistant Manager – Production

  • Department: Production
  • Role: Supervision of overall production activities
  • Experience: 10–12 years
  • Education/Qualification: B.Pharm, M.Pharm

Executive / Sr. Executive – Production (Compression/Coating)

  • Department: Production
  • Role: Compression/Coating process area supervision, documentation, USFDA compliance
  • Experience: 4–7 years
  • Education/Qualification: B.Pharm, M.Pharm, M.Sc

Operator – Production (Coating/Capsule Milling)

  • Department: Production
  • Role: Coating/Capsule Milling machine operation (fully automatic)
  • Experience: 3–7 years

Executive / Sr. Executive – Production Packaging

  • Department: Production-Packaging
  • Role: Primary & secondary bottle packing on CVC line, documentation, USFDA compliance
  • Experience: 4–7 years
  • Education/Qualification: B.Pharm, M.Pharm, M.Sc

Operator – Production Packaging

  • Department: Production-Packaging
  • Role: Primary & secondary bottle packing area, CVC line machine operation
  • Experience: 4–7 years

Executive / Sr. Executive – Central Validation Lab (AMV/AMT)

  • Department: Central Validation Lab
  • Role: Method validation & transfer, HPLC/GC, assay/impurities, dissolution & solvents, GLP & ICH
  • Experience: 4–7 years
  • Education/Qualification: B.Sc, M.Sc

Asst. Manager – QC

  • Department: Quality Control
  • Role: Review of QC records, GLP section, QMS investigation
  • Experience: 8–10 years
  • Education/Qualification: M.Sc, B.Pharm, M.Pharm

Officer / Executive / Sr. Executive – QC

  • Department: Quality Control
  • Role: Analysis of RM/FP/Stability by HPLC/GC
  • Experience: 3–8 years
  • Education/Qualification: M.Sc, B.Pharm, M.Pharm

Executive / Sr. Executive – Microbiology

  • Department: Microbiology
  • Role: MLT, Water Testing, EM, Method Validation
  • Experience: 4–7 years
  • Education/Qualification: M.Sc (Microbiology)

Asst. Manager – QA

  • Department: Quality Assurance
  • Role: QMS, Cleaning validation, Training Management, IPQA, AQA
  • Experience: 8–10 years
  • Education/Qualification: B.Pharm, M.Pharm, M.Sc

Officer / Executive / Sr. Executive – QA

  • Department: Quality Assurance
  • Role: Documentation, QMS, Validation and Qualification, AQA
  • Experience: 3–4 years
  • Education/Qualification: B.Pharm, M.Pharm

Skills/Qualifications

  • Strong experience in USFDA-regulated manufacturing and documentation practices
  • Proficiency in GMP, GLP, ICH guidelines, and regulatory compliance
  • Hands-on knowledge of HPLC, GC, analytical method validation, and stability studies
  • Expertise in compression, coating, capsule milling, and automated CVC bottle packing lines
  • Experience in QMS, deviation/investigation handling, cleaning validation, and training
  • Team supervision and problem-solving skills in a fast-paced pharma environment
  • Relevant pharmaceutical or science degree with proven industry track record

Key Responsibilities

  • Supervise daily production and packaging operations while ensuring USFDA compliance
  • Perform and review analytical testing, method validation, and transfer activities
  • Handle documentation, QMS investigations, and quality record reviews
  • Operate and maintain fully automatic coating, milling, and CVC packing machines
  • Conduct microbiology testing including MLT, water analysis, and environmental monitoring
  • Support cleaning validation, training management, and qualification activities
  • Ensure timely reporting and adherence to international quality standards

Benefits/Perks

  • Excellent career growth opportunities in a globally expanding organization
  • Exposure to USFDA-approved facility and regulated international markets
  • Continuous learning in advanced pharma manufacturing and validation techniques
  • Collaborative and innovation-driven work culture
  • Competitive salary and industry-standard benefits
  • Long-term stability with a forward-looking pharmaceutical group

How to Apply

Share your updated resume at career@senorespharma.com or call +91 91066 17844 if you cannot attend the walk-in.

Apnar Pharma Walk-in Interview on 12 April 2026

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Don’t miss this opportunity — update your CV and prepare for a promising step in your pharmaceutical career!

Walk-in Interview Details

  • Date: 12 April 2026 (Sunday)
  • Time: 10:00 AM to 03:00 PM
  • Venue: Ginger RCR, 9, Race Course Rd, Near RBL Bank, Gadapura, Diwalipura, Vadodara, Gujarat-390007
  • Contact/Email: career@senorespharma.com | +91 91066 17844
  • Job Location: Apnar Pharma Plant, Block No. 102, Gavasad, Padra, Vadodara-391430, Gujarat

Why You Should Join

Apnar Pharma, backed by Senores Pharmaceuticals, offers a dynamic environment focused on quality, compliance, and innovation. Professionals joining now will benefit from long-term career stability, exposure to cutting-edge processes, and growth in regulated global markets.

The company’s commitment to high international standards creates an ideal setting for skill development and meaningful contributions to global healthcare.

FAQs

What qualifications are needed for these pharma jobs at Apnar Pharma?

Most roles require B.Pharm, M.Pharm, M.Sc, or B.Sc/M.Sc (Microbiology) with relevant experience in pharmaceutical manufacturing or quality.

Is USFDA experience mandatory?

Experience in USFDA/GMP-compliant environments is highly preferred, especially for production, QA, QC, and validation roles.

Are freshers eligible for the walk-in interview?

No. All positions require a minimum of 3 years of relevant experience.

What growth opportunities does Apnar Pharma offer?

Candidates can expect rapid career progression, international exposure, and involvement in new product launches within a growing regulated-market focused company.

Where exactly is the plant located?

The manufacturing facility is at Gavasad on Padra Jambusar Road, Taluka Padra, Vadodara district, Gujarat.

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