Stallion Laboratories Pvt. Ltd., a USFDA-approved pharmaceutical manufacturing company, has announced a major hiring drive for experienced pharma professionals. The company is inviting applications for various positions across Production, Packing, Warehouse, Engineering, Quality Control (QC), Quality Assurance (QA), ADL, and Corporate Quality Assurance (CQA) departments at its Unit-II facility in Ahmedabad, Gujarat.

This recruitment drive offers excellent opportunities for Diploma, ITI, B.Pharm, M.Pharm, M.Sc., B.Sc., and B.Com graduates seeking growth in a regulated pharmaceutical manufacturing environment.

Company Overview

Company Name: Stallion Laboratories Pvt. Ltd.

Industry: Pharmaceutical Manufacturing

Facility Type: USFDA Approved Manufacturing Unit

Location: Ahmedabad, Gujarat, India

Stallion Laboratories is known for its commitment to quality, regulatory compliance, and manufacturing excellence. The organization offers a professional work environment with strong career growth opportunities.

Available Departments & Open Positions

1. Production Department

Qualification

Experience

Designation

Required Skills

Diploma / ITI

1–3 Years

FTE

Compression, Granulation

B.Pharm / M.Pharm

2–4 Years

Officer

QMS, BMR Preparation, BPR Preparation

2. Packing Department

Qualification

Experience

Designation

Required Skills

B.Pharm / M.Pharm

2–4 Years

Officer / Sr. Officer

Blister Packing, CVC Packing

3. Warehouse Department

Qualification

Experience

Designation

Required Skills

ITI / Diploma

2–4 Years

Technician / Operator

RM, PM & FG Warehouse Activities

B.Pharm / B.Sc / M.Sc / B.Com

10–12 Years

Manager

Warehouse Management, Pharma Cloud, FG Dispatch, Export Documentation

4. Engineering Department

Qualification

Experience

Designation

Required Skills

Second Class Boiler Operator

1–3 Years

Operator

Boiler Operations, ETP

5. Quality Control (QC)

Qualification

Experience

Designation

Required Skills

B.Pharm / M.Pharm / M.Sc

2–4 Years

Officer / Sr. Officer

AMV, AMT

B.Pharm / M.Pharm / M.Sc

2–4 Years

Officer / Sr. Officer

HPLC Analysis

B.Pharm / M.Pharm / M.Sc

8–10 Years

AM / DM

QMS, OOS, OOT, CAPA, GLP, Audit, Regulatory Compliance

B.Pharm / M.Pharm / M.Sc

8–10 Years

AM / DM

FP, FG Validation, HT, Cleaning Validation, In-Process Activities

6. Quality Assurance (QA)

Qualification

Experience

Designation

Required Skills

B.Pharm / M.Pharm

2–4 Years

Officer / Sr. Officer

IPQA

B.Pharm / M.Pharm

2–4 Years

Officer / Sr. Officer

Document Control, BMR/BPR Issuance, SOP Management

B.Pharm / M.Pharm

2–4 Years

Officer / Sr. Officer

Stability

B.Pharm / M.Pharm

7–8 Years

Executive

AQA

7. ADL (Analytical Development Laboratory)

Qualification

Experience

Designation

Required Skills

B.Pharm / M.Pharm / M.Sc

2–4 Years

Officer / Sr. Officer

Method Validation, Method Development

8. Corporate Quality Assurance (CQA)

Qualification

Experience

Designation

Required Skills

B.Pharm / M.Pharm

5–7 Years

Executive

GMP Compliance, QMS Management

Required Documents

Candidates should keep the following documents ready:

Updated Resume/CV

Last Three Months Salary Slips

Appointment Letter

Current CTC Structure

Educational Certificates

Experience Certificates

Government ID Proof

Company Address

Stallion Laboratories Pvt. Ltd. – Unit II

Gallops Industrial Park II, D-4,5,6,17,18,19

Opp. Meldi Mata Mandir,

Vasana, Chacharwadi, Changodar, Bavla,

Ahmedabad – 382110, Gujarat, India

Contact Details

Email ID: paresh.patel@stallionlabs.com

Mobile Number: 9104744518

Why Join Stallion Laboratories?

USFDA-approved manufacturing facility

Career growth opportunities

Exposure to global regulatory standards

Modern pharmaceutical manufacturing environment

Strong quality and compliance culture

Equal Opportunity Employer

Technical FAQs

1. What is BMR and BPR in pharmaceutical manufacturing?

BMR (Batch Manufacturing Record) and BPR (Batch Packaging Record) are controlled documents used to record manufacturing and packaging activities. They ensure product traceability, GMP compliance, and regulatory adherence.

2. What is HPLC analysis in Quality Control?

High Performance Liquid Chromatography (HPLC) is an analytical technique used to identify, quantify, and verify pharmaceutical compounds, impurities, and finished products according to approved specifications.

3. What is the difference between OOS and OOT investigations?

OOS (Out of Specification): Test result falls outside approved limits.

OOT (Out of Trend): Test result is within specification but shows unusual variation compared to historical data.

4. What is CAPA in pharmaceutical quality systems?

CAPA (Corrective and Preventive Action) is a structured process used to investigate deviations, identify root causes, implement corrections, and prevent recurrence to maintain product quality and compliance.

5. What is Method Validation in ADL?

Method Validation confirms that an analytical method consistently produces accurate, precise, specific, robust, and reproducible results suitable for its intended pharmaceutical application.