APDM Pharmaceuticals Pvt. Ltd. has announced a Walk-In Interview for multiple Quality Control (QC) positions. This recruitment drive is an excellent opportunity for Freshers and experienced professionals (up to 8 years) who are looking to build a career in the pharmaceutical quality domain. Candidates with M.Pharm or M.Sc. (Organic Chemistry) qualifications are invited to attend the interview.

If you are passionate about pharmaceutical quality systems, laboratory analysis, and regulatory compliance, this walk-in drive could be the right opportunity for you.

Job Overview

Particular Details

Company Name

APDM Pharmaceuticals Pvt. Ltd.

Job Type

Walk-In Interview

Department

Quality Control (QC)

Designation

Trainee to Sr. Executive

Experience

Freshers to 8 Years

Qualification

M.Pharm, M.Sc. (Organic Chemistry)

Walk-In Date

22 July 2026 (Wednesday)

Interview Time

1:00 PM to 4:00 PM

Job Location

Ahmedabad, Gujarat, India

Departments Hiring

1. QC Documentation

Responsibilities include:

Documentation management

Review and compliance

Data Integrity

GMP documentation practices

2. QC – QMS

Key responsibilities:

Quality Management System (QMS)

SOP preparation and review

Record management

Compliance with audits and regulatory requirements

3. HPLC & GC Analysis

Candidates should have knowledge of:

HPLC operation

Gas Chromatography (GC)

Method development

Sample analysis

Result interpretation and reporting

Eligibility Criteria

Candidates should possess:

M.Pharm

M.Sc. (Organic Chemistry)

Experience:

Freshers are eligible.

Candidates with up to 8 years of pharmaceutical QC experience can apply.

Walk-In Interview Details

Date: 22 July 2026 (Wednesday)

Time: 1:00 PM – 4:00 PM

Venue: APDM Pharmaceuticals Pvt. Ltd.

Sakodara, Ahmedabad – 382210, Gujarat, India

Resume Submission

Candidates who are unable to attend may send their resumes to:

Email: career@apdmpharma.com

Email Subject: Application – QC – [Position]

Important Note

Candidates who have already attended an interview at APDM Pharmaceuticals are requested not to attend again.

Carry updated resume, educational certificates, experience documents (if applicable), passport-size photographs, and government-issued ID proof.

Why Join APDM Pharmaceuticals?

APDM Pharmaceuticals promotes a professional work culture based on:

Quality

Integrity

Innovation

Teamwork

The organization provides opportunities to work in regulated pharmaceutical manufacturing with exposure to GMP, GLP, quality systems, and modern analytical instruments.

5 Technical FAQs

1. What is the role of HPLC in Quality Control?

Answer: High Performance Liquid Chromatography (HPLC) is used to identify, separate, and quantify pharmaceutical compounds. It ensures products meet quality specifications and regulatory requirements.

2. What is Data Integrity in pharmaceutical QC?

Answer: Data Integrity ensures laboratory data is complete, accurate, consistent, and attributable throughout its lifecycle. It follows ALCOA+ principles and is essential for regulatory compliance.

3. What is the purpose of a Quality Management System (QMS)?

Answer: A QMS establishes procedures for document control, deviations, CAPA, change control, training, and audits to maintain product quality and regulatory compliance.

4. What is the difference between HPLC and GC?

Answer: HPLC analyzes non-volatile or thermally unstable compounds using a liquid mobile phase, while Gas Chromatography (GC) is used for volatile compounds with a gaseous mobile phase.

5. Why are SOPs important in pharmaceutical laboratories?

Answer: Standard Operating Procedures (SOPs) provide standardized instructions for laboratory activities, ensuring consistency, compliance with GMP/GLP guidelines, improved data reliability, and reduced operational errors.