Stallion Laboratories Pvt. Ltd. has announced a Walk-In Interview Drive for experienced pharmaceutical professionals at its Unit II manufacturing facility in Changodar, Ahmedabad, Gujarat. The company is inviting applications for multiple positions in Production, Packing, Warehouse, Engineering, Quality Assurance (QA), and Corporate Quality Assurance (CQA).

Candidates with B.Pharm, M.Pharm, B.Sc, B.Com, ITI, Diploma, and Second Class Boiler Operator Certification along with relevant pharmaceutical experience are encouraged to apply.

Job Overview

Particular Details

Company Name

Stallion Laboratories Pvt. Ltd.

Job Type

Walk-In Interview / Email Application

Industry

Pharmaceutical Manufacturing

Job Location

Changodar, Ahmedabad, Gujarat

Experience

2–6 Years

Employment Type

Full Time

Department-wise Vacancy Details

1. Production

Qualification: B.Pharm / M.Pharm

Experience: 2–4 Years

Designation: Officer / Senior Officer

Required Skill: QMS (Quality Management System)

2. Packing

Qualification: B.Pharm

Experience: 2–4 Years

Designation: Officer / Senior Officer

Skills Required:

Blister Packing

CVC Packing

3. Warehouse

Operator/FTE

Qualification: ITI / Diploma

Experience: 2–4 Years

Designation: FTE / Operator

Skills:

Raw Material (RM)

Packing Material (PM)

Finished Goods (FG)

Officer/Senior Officer

Qualification: B.Sc / B.Com

Experience: 2–4 Years

Designation: Officer / Senior Officer

Skills:

Warehouse Activities

RM, PM & FG Handling

Dispensing

4. Engineering

Qualification: Second Class Boiler Operator Certificate

Experience: 2–4 Years

Designation: Technician / Operator

Skill Required: Boiler Operations

5. Quality Assurance (QA)

Qualification: B.Pharm / M.Pharm

Experience: 2–4 Years

Designation: Officer / Senior Officer

Skill Required: Stability Management

6. Corporate Quality Assurance (CQA)

Qualification: B.Pharm / M.Pharm

Experience: 4–6 Years

Designation: Senior Officer / Executive

Skill Required:

Audit

Compliance

Required Documents

Candidates should send the following documents:

Updated Resume

Passport Size Photograph

Educational Certificates

Experience Certificates

Last 3 Months Salary Slips

Current CTC

Expected CTC

Aadhaar Card

PAN Card

Email ID for Application

Send your updated CV to:

paresh.patel@stallionlabs.com

aarti.oberoi@stallionlabs.com

Contact Numbers:

9104744518

9409309964

Company Address

Stallion Laboratories Pvt. Ltd. – Unit II

Gallops Industrial Park II,

D-4, 5, 6, 17, 18 & 19,

Opp. Meldi Mata Mandir,

Vasna-Chacharwadi,

Changodar, Bavla,

Ahmedabad – 382110,

Gujarat

Why Join Stallion Laboratories?

Reputed pharmaceutical manufacturing company

Career growth opportunities

Exposure to GMP-compliant manufacturing

Professional work environment

Opportunities across Production, QA, Warehouse, Engineering, and Packing

Technical FAQs

1. What is QMS in pharmaceutical manufacturing?

QMS (Quality Management System) ensures that pharmaceutical products are consistently manufactured and controlled according to GMP requirements through proper documentation, deviations, CAPA, change control, and risk management.

2. What is the role of Stability Management in QA?

Stability Management involves monitoring drug products under defined storage conditions to determine shelf life, ensuring quality, safety, and efficacy throughout the product’s lifecycle as per ICH guidelines.

3. What are RM, PM, and FG in Warehouse operations?

RM: Raw Materials used in manufacturing.

PM: Packing Materials used for packaging.

FG: Finished Goods ready for distribution after quality approval.

4. What is CVC Blister Packing?

CVC (Continuous Vertical Cartoner/Packaging System) blister packing is an automated pharmaceutical packaging process used to pack tablets and capsules into blister packs with high accuracy, productivity, and GMP compliance.

5. What are GMP Audit and Compliance responsibilities in CQA?

CQA professionals conduct internal audits, monitor regulatory compliance, review SOPs, investigate deviations, oversee CAPA implementation, and ensure adherence to GMP, WHO, and regulatory standards.