Halewood Laboratories Pvt. Ltd. has announced a Walk-In Drive 2026 for experienced professionals across multiple pharmaceutical departments. The recruitment drive will be held in Ahmedabad, Gujarat, offering opportunities in Quality Assurance, Quality Control, Production & Packing, Engineering, R&D, and Regulatory Affairs.

If you have experience in the pharmaceutical industry and are looking for career growth with a reputed organization, this walk-in interview is an excellent opportunity.

Walk-In Drive Details

Particular Details

Company Name

Halewood Laboratories Pvt. Ltd.

Job Type

Walk-In Interview

Interview Date

28th June 2026 (Sunday)

Time

09:00 AM – 04:00 PM

Interview Venue

Sachi Banquet, Hotel Binori, Thaltej, Ahmedabad, Gujarat

Job Location

Ahmedabad, Gujarat

Current Openings

Quality Assurance (QA)

QMS Lead – AM (10+ Years)

QMS Executive – Pharma Cloud, Artwork, Masters Review (4–6 Years)

QMS & Technology Transfer Executive (4–6 Years)

Validation & Qualification Lead – Up to AM (10+ Years)

QMS Documentation Executive / Sr. Executive (4–6 Years)

IPQA Shift Incharge – Executive (5 Years)

Engineering

Electrician – Plant Maintenance

Officer – Plant Maintenance

Officer / Sr. Officer – Civil

Fitter – Plant Maintenance

Production & Packing

Operators

Qualification: 12th / ITI / Diploma

Experience: 2–10 Years

Departments:

Manufacturing

Filling

Blister

Sachet Packing

Track & Trace

Washing Machine

Granulation

Officers / Supervisors

Qualification:

B.Pharm

M.Pharm

B.Sc

M.Sc

Experience: 2–5 Years

Departments:

Granulation

Liquid & Topical Manufacturing

Production QMS

Packing

Quality Control (QC)

Position: QC Analyst (Officer / Sr. Officer)

Experience: 1–5 Years

Sections:

GLP

PM

FP

Research & Development (R&D)

TT Documentation (1–5 Years)

ADL Executive (5 Years)

DQA (1–5 Years)

F&D Executive (2–5 Years)

Regulatory Affairs

Executive / Senior Executive

Experience: 3–7 Years

How to Apply

Candidates who meet the eligibility criteria can directly attend the walk-in interview with:

Updated Resume/CV

Educational Certificates

Experience Certificates

Latest Passport Size Photographs

Government Photo ID Proof

Latest Salary Documents (if applicable)

Resume Email: hr.halewoodlabs@gmail.com

Contact Number: +91 63563 364656

Why Join Halewood Laboratories?

Reputed pharmaceutical company

Career growth opportunities

Multiple technical departments

Professional working environment

Opportunities for experienced pharma professionals

Technical FAQs

1. What is IPQA and why is it important in pharmaceutical manufacturing?

Answer: In-Process Quality Assurance (IPQA) ensures manufacturing activities comply with GMP guidelines through continuous monitoring, process verification, line clearance, and documentation to maintain product quality.

2. What does Validation & Qualification involve in a pharma plant?

Answer: Validation confirms that manufacturing processes consistently produce quality products, while equipment qualification (DQ, IQ, OQ, PQ) verifies that machinery performs according to predefined specifications.

3. What is the role of GLP in Quality Control?

Answer: Good Laboratory Practices (GLP) ensure laboratory testing is accurate, reliable, traceable, and compliant with regulatory standards through proper documentation and validated analytical procedures.

4. What is Technology Transfer (TT) in pharmaceutical manufacturing?

Answer: Technology Transfer is the structured process of transferring product knowledge, manufacturing methods, analytical procedures, and process parameters from R&D to commercial production while maintaining product quality and regulatory compliance.

5. What are the responsibilities of Regulatory Affairs professionals?

Answer: Regulatory Affairs professionals prepare and maintain product dossiers, ensure compliance with national and international regulations, coordinate with health authorities, manage product registrations, and support audits and regulatory submissions.