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Halewood Laboratories Pvt. Ltd. Announces Walk-In Interview Drive for Multiple Roles – 21st March 2026
Halewood Laboratories Pvt. Ltd., a rapidly growing pharmaceutical manufacturing company, has announced a walk-in interview drive to hire talented professionals across multiple departments. The company is also extending opportunities to freshers looking to begin their careers in the pharmaceutical industry.
Walk-In Interview Details
Date: 21st March 2026
Time: 09:00 AM to 04:00 PM
Venue:
Sub Plot No. 10, Unit No. 27,
Insta Industrial Park, Bavla,
Halewood Laboratories Pvt. Ltd.
Opportunities for Freshers
Halewood Laboratories is inviting applications from fresh graduates including:
B. Pharma
M. Pharma
M.Sc.
Selected candidates may be offered roles as Apprentices, providing a strong foundation to build a successful pharmaceutical career.
Departments & Open Positions
Quality Assurance (QA)
QMS Lead (AM) – 10–13 years
QMS Sr. Executive – 5–7 years
AM – Validation & Documentation – 9+ years
IPQA Executive / Sr. Executive – 3–5 years
Quality Control (QC)
RM Analysis – 2–6 years
PM Analysis – 2–4 years
IP/FP Analysis – 2–6 years
Stability Analysis – 2–6 years
Water Analysis – 2–4 years
Reviewer – 5–9 years
QC-QMS – 6–9 years
AMV / AMT Analyst – 4–7 years
Sampling Person – Fresher
Production
Granulation Operator – 2–10 years
Liquid Manufacturing Operator – 2–10 years
Cream/Ointment Manufacturing Operator – 2–10 years
Granulation Supervisor – 2–10 years
Liquid Manufacturing Supervisor – 2–10 years
Cream/Ointment Manufacturing Supervisor – 2–10 years
Production QMS – 2–10 years
Packing
Sachet Operator – 4–8 years
Track & Trace Operator – 4–9 years
Packing Operator – 4–10 years
Packing Supervisor – 4–11 years
Warehouse
Officer / Senior Officer – 2–4 years
Executive / Sr. Executive – 4+ years
Engineering
HVAC Operator – 2–5 years
Plant Maintenance – 2–5 years
Technician – Instrument – 3–5 years
Fitter Utility – 1–3 years
Utility Executive – 4–7 years
Boiler Operator – 3–5 years
ADL (Analytical Development Laboratory)
Executive / Sr. Executive – 3+ years
F&D (Formulation & Development)
Executive / Sr. Executive – 3+ years
Why Join Halewood Laboratories?
Halewood Laboratories offers a dynamic work environment, exposure to advanced pharmaceutical manufacturing processes, and opportunities for both experienced professionals and freshers to grow within the organization.
Contact Information
Phone: 63563 64656
Email: hr.halewoodlabs@gmail.com
FAQ:
1. What is IPQA and what are its key responsibilities in pharmaceutical manufacturing?
Answer:
In-Process Quality Assurance (IPQA) ensures that manufacturing processes comply with GMP standards during production. Key responsibilities include line clearance, in-process checks, monitoring critical parameters, reviewing batch records, and ensuring adherence to SOPs to maintain product quality.
2. What are the differences between RM, PM, and FP analysis in Quality Control?
Answer:
RM (Raw Material): Testing of incoming raw materials before use.
PM (Packing Material): Testing packaging components like bottles, strips, and labels.
FP (Finished Product): Final testing of the manufactured product before market release.
Each stage ensures quality and compliance with pharmacopeial standards.
3. What is process validation and why is it important?
Answer:
Process validation is documented evidence that a manufacturing process consistently produces a product meeting its predetermined specifications. It is important to ensure product quality, regulatory compliance, and reproducibility of results across batches.
4. What are common instruments used in QC and ADL labs?
Answer:
Common instruments include HPLC, GC, UV-Visible Spectrophotometer, Dissolution Apparatus, FTIR, and Karl Fischer titrator. These instruments are used for qualitative and quantitative analysis of pharmaceutical substances.
5. What is the role of HVAC in pharmaceutical manufacturing?
Answer:
HVAC (Heating, Ventilation, and Air Conditioning) systems control environmental conditions such as temperature, humidity, and air cleanliness. It helps maintain cleanroom classifications, prevents contamination, and ensures compliance with regulatory standards like GMP.
