Accuprec Research Labs Walk-In Interview for Analytical Development & Quality Control

Accuprec Research Labs Pvt. Ltd., a leading pharmaceutical research and analytical testing organization, has announced a Walk-In Interview Drive for multiple positions in the Analytical Development (ADL) and Quality Control (QC) departments. The recruitment is being conducted to support the company’s ongoing expansion and offers excellent career opportunities for freshers and experienced professionals in the pharmaceutical and analytical research sectors.

Candidates with qualifications such as B.Sc, M.Sc, B.Pharm, M.Pharm, BCA, BA, and B.Com can participate in the interview process based on the role requirements.

About Accuprec Research Labs

Accuprec Research Labs Pvt. Ltd. is a reputed analytical research and testing organization providing services in pharmaceutical analysis, method development, validation, impurity profiling, stability studies, and regulatory support. The company is known for its advanced analytical infrastructure and compliance with global quality standards.

Walk-In Interview Overview

Company Name

Accuprec Research Labs Pvt. Ltd.

Department

Analytical Development & Quality Control

Job Type

Permanent

Interview Date

6th June 2026

Interview Mode

Walk-In

Industry

Pharmaceutical / Analytical Research

Location

Ahmedabad, Gujarat

Available Positions

Quality Control (COA Preparation)

Experience: 0–1 Year

Qualification:

BA

B.Com

BCA

B.Sc

B.Pharm

Equivalent Qualification

Analytical & Instrumentation Roles

Experience: 3–5 Years

Positions include:

HPLC & IC – QC

HPLC – AMV

LC-MS/MS – QC + AMV

LC-MS/Q-TOF

GC – QC + AMV

GC-MS/MS – QC + AMV

Qualification:

B.Sc

M.Sc

B.Pharm

M.Pharm

Equivalent Qualification

ICP Analysis Roles

Experience: 3–5 Years

Positions:

ICP-OES – QC + AMV

ICP-MS – QC + AMV

Qualification:

B.Sc

M.Sc

B.Pharm

M.Pharm

Equivalent Qualification

Wet Lab & Particle Size Distribution

Experience: 1–3 Years

Positions:

Wet Lab Analyst

PSD (Malvern & Zeta Potential)

Qualification:

B.Sc

M.Sc

B.Pharm

M.Pharm

Equivalent Qualification

Reviewer & Documentation Roles

Experience: 5–8 Years

Positions:

Reviewer – QC

Reviewer – AMV

Reviewer – GC / GC-MS

Reviewer – QC (GLP Activities)

Documentation – AMV

Qualification:

B.Sc

M.Sc

B.Pharm

M.Pharm

Equivalent Qualification

Skills Preferred

Candidates having hands-on experience with the following analytical instruments will be preferred:

HPLC

IC (Ion Chromatography)

LC-MS/MS

Q-TOF

GC & GC-MS/MS

ICP-OES

ICP-MS

Particle Size Analyzer (Malvern)

Zeta Potential Analyzer

Method Development & Validation

GLP Documentation

Why Join Accuprec Research Labs?

Opportunity to work with advanced analytical technologies.

Exposure to regulated pharmaceutical projects.

Career growth in analytical research and quality control.

Learning environment with experienced scientists and researchers.

Expansion-driven hiring with multiple openings.

Selection Process

The recruitment process may include:

Technical Discussion

Instrumentation Knowledge Assessment

HR Interaction

Final Selection

Candidates should carry updated resumes, educational certificates, experience documents, and identity proof during the interview.

Technical FAQs

1. What is the difference between HPLC and LC-MS/MS?

HPLC separates compounds based on their chemical properties, while LC-MS/MS combines liquid chromatography with mass spectrometry for highly sensitive identification and quantification of analytes, impurities, and trace compounds.

2. What is Q-TOF in pharmaceutical analysis?

Q-TOF (Quadrupole Time-of-Flight) is an advanced mass spectrometry technique used for accurate mass determination, impurity characterization, metabolite identification, and structural elucidation.

3. Why is ICP-MS preferred for elemental impurity analysis?

ICP-MS offers extremely low detection limits and can accurately measure trace metal impurities as per ICH Q3D guidelines, making it one of the most reliable techniques for pharmaceutical elemental analysis.

4. What is AMV in analytical laboratories?

AMV stands for Analytical Method Validation. It is the process of demonstrating that an analytical method consistently produces reliable, accurate, precise, and reproducible results according to regulatory requirements.

5. What is the role of GLP in Quality Control laboratories?

Good Laboratory Practice (GLP) ensures data integrity, documentation accuracy, instrument compliance, and standardized laboratory procedures, helping organizations meet regulatory expectations and maintain product quality.

Disclaimer: Candidates are advised to verify all recruitment details directly with the company before attending the interview. Selection and hiring decisions are solely at the discretion of Accuprec Research Labs Pvt. Ltd.