Amoli Organics, a division of Umedica Laboratories Pvt. Ltd., has announced a Walk-in Interview for experienced professionals in Analytical Research & Development (ARD/ADL), Chemical Research & Development (CRD), and Quality Control (QC). This recruitment is aimed at candidates with API pharmaceutical experience, particularly in Oncology for ARD and CRD roles.

If you have experience in API manufacturing, analytical research, process development, or quality control, this is an excellent opportunity to join one of the leading pharmaceutical organizations in Gujarat.

Job Overview

Particular Details

Company Name

Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.)

Job Type

Walk-in Interview

Walk-in Date

26 July 2026 (Sunday)

Interview Time

09:00 AM to 12:00 PM

Job Location

Amoli Organics, 422 ECP Canal Road, Village Luna, Ta. Padra, Dist. Vadodara, Gujarat – 391440

Interview Venue

Baroda Productivity Council, Productivity House, 2nd Floor, BPC Road, Alkapuri, Vadodara, Gujarat – 390007

Preferred Candidates

Only Male Candidates

Department-wise Vacancy Details

1. ARD / ADL (Analytical Research & Development)

Qualification

M.Sc / Ph.D

Experience

2 to 5 Years

Required Skills

API Oncology product analysis

Routine analytical testing

HPLC

Gas Chromatography (GC)

Wet Chemistry

Analytical Method Development

Method Validation

Analytical Documentation

Important: Oncology background is mandatory for ARD candidates.

2. CRD (Chemical Research & Development)

Qualification

M.Sc / Ph.D

Experience

1 to 6 Years

Required Skills

API synthesis of Oncology molecules

Isolator system handling

API process development

Process optimization

Technology transfer

Technical documentation

Experimental record preparation

Important: Oncology background is mandatory for CRD candidates.

3. Quality Control (QC)

Qualification

M.Sc. (Chemistry)

Experience

1 to 12 Years

Required Skills

UV Spectrophotometer

FTIR

Malvern 3000

Karl Fischer

Potentiometer

Polarimeter

HPLC Operation & Calibration

Preparation of Specifications

MOA

Analytical Worksheets

QMS Documentation

Note: Candidates should have experience only in the API industry.

Walk-in Interview Details

Date: 26 July 2026

Time: 09:00 AM to 12:00 PM

Interview Venue: Baroda Productivity Council, Productivity House, 2nd Floor, BPC Road, Alkapuri, Vadodara, Gujarat – 390007

Job Location

Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.)

422 ECP Canal Road, Village Luna, Ta. Padra, District Vadodara, Gujarat – 391440

Documents to Carry

Updated Resume/CV

Educational Certificates

Experience Certificates

Latest Salary Slips (if available)

Government Photo ID

Passport-size Photographs

Why Join Amoli Organics?

Opportunity to work with a reputed pharmaceutical API manufacturer.

Exposure to Oncology API research and manufacturing.

Professional growth in R&D and Quality Control.

Work with advanced analytical instruments and GMP-compliant systems.

Excellent career prospects in the pharmaceutical sector.

Technical FAQs

1. What is the role of HPLC in pharmaceutical quality control?

HPLC (High Performance Liquid Chromatography) is used for identification, assay, impurity profiling, stability studies, and quality evaluation of pharmaceutical products.

2. Why is analytical method validation important?

Method validation ensures analytical methods are accurate, precise, specific, robust, and suitable for regulatory compliance according to ICH guidelines.

3. What is the purpose of Karl Fischer titration?

Karl Fischer titration is used to determine moisture content accurately in APIs and pharmaceutical raw materials.

4. What is technology transfer in API manufacturing?

Technology transfer is the systematic process of transferring product and manufacturing knowledge from R&D to commercial production while maintaining product quality and consistency.

5. Why is Oncology API experience mandatory for ARD and CRD roles?

Oncology APIs require specialized handling due to their high potency. Professionals must understand containment systems, safety protocols, process development, analytical testing, and regulatory compliance specific to oncology products.