Apnar Walk-In Production, QA, QC & Microbiology

Apnar Pharma Walk-In Interview 2026 | 25+ Vacancies in Production, QA, QC & Microbiology

Apnar Pharma Private Limited, a subsidiary of Senores Pharmaceuticals, is conducting a walk-in interview for multiple vacancies across Production, Quality Assurance, Quality Control, Microbiology, and Validation departments at its Vadodara facility. The company is offering more than 25 openings ranging from Operator to Assistant Manager positions, making this a high-value opportunity for experienced pharma professionals.

This hiring drive is scheduled on 12th April 2026 in Vadodara, Gujarat, and is ideal for candidates with 3 to 12 years of experience in regulated pharmaceutical manufacturing, especially those with exposure to USFDA compliance, GMP systems, and formulation production.

Company Overview

Apnar Pharma Private Limited operates under Senores Pharmaceuticals, a globally recognized research-driven pharmaceutical company. The organization focuses on developing and manufacturing high-quality pharmaceutical products for regulated markets such as the US and Canada, along with emerging markets worldwide.

With a strong emphasis on regulatory compliance, innovation, and quality systems, the company provides a robust platform for professionals to grow in areas like formulation development, quality assurance, validation, and pharmaceutical manufacturing operations.

Job Role & Responsibilities

Production Department

• Supervise manufacturing activities including compression, coating, and capsule filling
• Handle documentation and ensure compliance with GMP and USFDA guidelines
• Operate automated equipment and maintain batch production records

Packaging Department

• Manage primary and secondary bottle packing operations
• Handle CVC line operations and packaging documentation
• Ensure regulatory compliance in packaging processes

Quality Control (QC)

• Perform analysis of raw materials, finished products, and stability samples
• Operate analytical instruments such as HPLC and GC
• Maintain documentation, support investigations, and ensure GLP compliance

Microbiology

• Conduct environmental monitoring (EM) and water testing
• Perform microbial limit testing (MLT)
• Support method validation and microbiological analysis

Quality Assurance (QA)

• Handle QMS documentation, validation, and qualification activities
• Manage IPQA, AQA, and cleaning validation processes
• Ensure compliance with regulatory and quality standards

Validation (Central Lab)

• Perform method validation and transfer activities
• Work on analytical validation using HPLC/GC techniques
• Ensure compliance with ICH and GLP guidelines

Eligibility / Qualifications

Required Education

B.Pharm, M.Pharm, M.Sc, ITI

Relevant Courses

Pharmaceutical Sciences, Microbiology, Biotechnology, Analytical Chemistry, Industrial Pharmacy, Quality Assurance, Process Engineering

Experience

• Operator Roles: 3–7 years
• Executive Roles: 3–8 years
• Assistant Manager Roles: 8–12 years
• Experience in USFDA-regulated pharma environment preferred

Skills Required

• Strong knowledge of GMP, GLP, and regulatory compliance
• Experience in pharmaceutical manufacturing and quality systems
• Hands-on expertise in HPLC, GC, validation, or production equipment
• Good documentation and audit readiness skills

Location & Salary

Job Location

Apnar Pharma Pvt. Ltd., Vadodara, Gujarat

Salary

• Competitive salary based on experience and designation
• Additional benefits as per company policy

Application Process

Walk-In Interview Details

• Date: 12th April 2026 (Sunday)
• Time: 10:00 AM to 03:00 PM
• Venue: Ginger Hotel, Race Course Road, Vadodara, Gujarat

Alternative Application

Candidates unable to attend can email their CV to:

• career@senorespharma.com

Contact Details

• Phone: +91 91066 17844

Why This Opportunity Matters

• Work with a global pharmaceutical company serving regulated markets
• Exposure to USFDA compliance and advanced manufacturing systems
• Career growth in QA, QC, production, and validation domains
• Opportunity to work in high-demand pharma roles with long-term stability

FAQs

How many vacancies are available?

There are 25+ vacancies across multiple departments.

What qualifications are required?

B.Pharm, M.Pharm, M.Sc, and ITI candidates are eligible.

What experience is required?

3 to 12 years depending on the role.

Is USFDA experience required?

Preferred but not mandatory for all roles.

How can I apply?

Attend the walk-in interview or email your CV to the provided address.

Summary Table

Company	Apnar Pharma Pvt. Ltd.
Vacancies	Production, QA, QC, Microbiology, Validation Roles
Required Education	B.Pharm, M.Pharm, M.Sc, ITI
Experience	3–12 Years