Join Halewood Laboratories Pvt. Ltd., a leading pharmaceutical manufacturer established in 1984, headquartered in Ahmedabad, Gujarat, with a revenue of ₹341 Cr (FY 2023). Specializing in contract manufacturing of tablets, capsules, and oral rehydration salts (ORS), Halewood operates a USFDA-compliant facility in Vatva GIDC, exporting to 40+ countries.

Rated 3.8/5 on AmbitionBox for job security (4.0/5), Halewood is hosting a walk-in interview on May 17, 2025, in Ahmedabad for roles in Quality Control (QC), Quality Management System (QMS), Corporate Quality Assurance (CQA), Validation, and Microbiological Analysis, targeting candidates with 0-10 years of experience in GMP-compliant OSD manufacturing.

Event Details: Walk-In Interview

This walk-in drive seeks professionals for Halewood’s Vatva facility, a GMP-compliant plant with a 75-lakh tablet/day capacity, focusing on raw material (RM), packing material (PM), in-process (IP), finished product (FP), process validation (PV), stability, QMS, CQA, and microbiological roles.

Date and Time

Date: Saturday, May 17, 2025
Time: 10:00 AM – 4:00 PM IST

Interview Venue

Hotel Aaram Orchard
Hitek Building, Bhagtacharya Rd, Near N.I.D, Opposite Museum, Paldi Gaam, Paldi, Ahmedabad, Gujarat – 380007

Work Location

Halewood Laboratories Pvt. Ltd.
319, GIDC Industrial Estate, Phase II, Vatva, Ahmedabad, Gujarat – 382445

Job Opportunities at Halewood Laboratories

We’re hiring for multiple roles across QC, QMS, CQA, Validation, and Microbiological sections to support OSD production at our Vatva facility, audited by SGS India for Canadian importers. Candidates with experience in RM/PM, IP/FP/PV, stability, and microbiological analysis are preferred.

1. Raw Material (RM)

Roles:
- Sampling: 0-1 years (M.Sc. Chemistry, B.Pharm)
- Analysis: 1-3 years (M.Sc. Chemistry, B.Pharm)
- Analysis (GC): 2-6 years (M.Sc. Chemistry, B.Pharm)
Vacancies: Multiple (likely 4-6)
Key Responsibilities:
- Sample RM per SOPs and perform chemical analysis
- Conduct GC testing for impurities and solvents
- Document results in Empower software per GLP
- Support RM release and audit preparations
Key Skills:
- Knowledge of GC, wet chemistry, and cGMP
- Proficiency in GLP and documentation
- Familiarity with 21CFR Part 211
Salary: ₹2.0–5.0 Lakhs/year (estimated for Ahmedabad)

2. Packing Material (PM)

Roles:
- Analysis: 0-2 years (M.Sc. Chemistry, B.Pharm)
- Section Head: 6-10 years (M.Sc. Chemistry, B.Pharm)
Vacancies: Multiple (likely 2-4)
Key Responsibilities:
- Test PM (blisters, foils) for quality and compliance
- Lead PM section, oversee testing, and train staff (Section Head)
- Document results per cGMP and support audits
- Ensure PM meets USFDA standards
Key Skills:
- Expertise in PM testing and cGMP
- Leadership and training skills (Section Head)
- Proficiency in documentation and audit readiness
Salary: ₹2.0–7.0 Lakhs/year (estimated for Ahmedabad)

3. In-Process/Finished Product/Process Validation (IP/FP/PV)

Roles:
- Analysis: 2-6 years (M.Sc. Chemistry, B.Pharm)
- Section Head: 6-10 years (M.Sc. Chemistry, B.Pharm)
Vacancies: Multiple (likely 4-6)
Key Responsibilities:
- Perform IP/FP testing using HPLC, UV, and dissolution
- Conduct PV to ensure process consistency
- Lead IP/FP/PV section and manage compliance (Section Head)
- Support batch release and USFDA audits
Key Skills:
- Expertise in HPLC, dissolution, and PV
- Knowledge of cGMP and ICH Q2(R1)
- Leadership and audit skills (Section Head)
Salary: ₹3.0–7.0 Lakhs/year (estimated for Ahmedabad)

4. Stability

Role: Analysis (2-6 years, M.Sc. Chemistry, B.Pharm)
Vacancies: Multiple (likely 2-4)
Key Responsibilities:
- Conduct stability studies per ICH Q1A(R2)
- Test samples using HPLC and walk-in stability chambers
- Document results and support audit readiness
- Ensure data integrity per cGMP
Key Skills:
- Expertise in stability testing and HPLC
- Knowledge of ICH guidelines and GLP
- Proficiency in data integrity and documentation
Salary: ₹3.0–5.5 Lakhs/year (estimated for Ahmedabad)

5. Quality Management System (QMS)

Role: QMS & Compliance (5-8 years, M.Sc. Chemistry, B.Pharm)
Vacancies: Multiple (likely 1-2)
Key Responsibilities:
- Manage QMS (deviations, CAPA, change controls)
- Ensure compliance with cGMP and USFDA standards
- Conduct internal audits and training
- Document QMS activities and support external audits
Key Skills:
- Expertise in QMS, CAPA, and cGMP
- Knowledge of QMS frameworks
- Strong documentation and audit skills
Salary: ₹5.0–8.0 Lakhs/year (estimated for Ahmedabad)

6. Reviewer (RM/IP/FP/PV/Stability)

Role: Reviewer (5-8 years, M.Sc. Chemistry, B.Pharm)
Vacancies: Multiple (likely 2-3)
Key Responsibilities:
- Review analytical data for RM, IP, FP, PV, and stability
- Ensure compliance with GLP and data integrity
- Support batch release and audit preparations
- Train junior analysts on review processes
Key Skills:
- Expertise in data review and GLP
- Knowledge of cGMP and 21CFR Part 11
- Strong analytical and training skills
Salary: ₹5.0–8.0 Lakhs/year (estimated for Ahmedabad)

7. Corporate Quality Assurance (CQA)

Role: Vendor Audit and Management (6-7 years, M.Sc. Chemistry, B.Pharm)
Vacancies: 1
Key Responsibilities:
- Conduct vendor audits for RM/PM suppliers
- Manage vendor qualification and compliance
- Document audit findings per cGMP
- Support USFDA and internal audits
Key Skills:
- Expertise in vendor audits and management
- Knowledge of cGMP and supplier quality
- Strong documentation and communication
Salary: ₹6.0–9.0 Lakhs/year (estimated for Ahmedabad)

8. Validation

Role: Analysis (2-6 years, M.Sc. Chemistry, B.Pharm)
Vacancies: Multiple (likely 2-3)
Key Responsibilities:
- Perform analytical method validation (AMV) per ICH Q2(R1)
- Conduct cleaning and process validation
- Document validation protocols and reports
- Support audit readiness and QMS
Key Skills:
- Expertise in AMV and cleaning validation
- Knowledge of ICH Q2(R1) and cGMP
- Proficiency in documentation and GLP
Salary: ₹3.0–5.5 Lakhs/year (estimated for Ahmedabad)

9. Microbiological

Role: Analysis (2-5 years, M.Sc. Microbiology)
Vacancies: Multiple (likely 2-3)
Key Responsibilities:
- Perform microbial limit tests (MLT) and environmental monitoring
- Conduct sterility and BET testing per USP
- Document results in ISO 7-compliant lab
- Support audit preparations and QMS
Key Skills:
- Expertise in MLT, BET, and EM
- Knowledge of USP, GLP, and ISO 7 norms
- Proficiency in microbiological documentation
Salary: ₹3.0–5.5 Lakhs/year (estimated for Ahmedabad)

Why Join Halewood Laboratories?

Halewood, with 348 employees, is rated 3.8/5 on AmbitionBox for job security (4.0/5) but criticized for work-life balance (3.5/5) due to shift schedules and a 1-month notice period for 60% of staff.

The Vatva facility, one of India’s largest ORS producers, supports anti-diabetic and antibiotic formulations, with no critical USFDA observations. Employees praise infrastructure (4.0/5) but note limited facilities (no free transport/canteen). With a 84.1% employee growth in 2024, Halewood offers stability in Ahmedabad’s pharma hub.

Key Benefits

Work in a USFDA-compliant OSD facility
Gain expertise in HPLC, GC, and microbiological testing
Contribute to exports for 40+ countries
Join a ₹341 Cr company with 41-year legacy
Access Ahmedabad’s vibrant pharma ecosystem

How to Apply

Attend the walk-in interview on May 17, 2025, from 10:00 AM to 4:00 PM at Hotel Aaram Orchard, Ahmedabad. Bring:

Updated resume with passport-size photo
Educational certificates (M.Sc., B.Pharm)
Experience certificates
Last 3 months’ payslips and latest increment letter
Aadhar and PAN card copies
Preparation:
- RM/PM/IP/FP/PV/Stability: Review HPLC, GC, and ICH Q2(R1)
- QMS/CQA: Study CAPA, vendor audits, and cGMP
- Microbiological: Focus on MLT, BET, and ISO 7
- Be ready for USFDA audit and data integrity questions
Note: Candidates unable to attend can email CVs to careers@halewoodlabs.com with subject “Position Name – Vatva” by May 15, 2025. Halewood does not charge recruitment fees; verify communications via @halewoodlabs.com emails.
Registration: No QR code mentioned; confirm with Halewood’s website or HR.

Halewood Laboratories Walk-In Interview for QC, QMS, CQA, Validation, and Microbiological Roles on 17th May

About Halewood Laboratories

Led by Kaushik Shantilal Chaturvedi, Halewood operates a 75-lakh tablet/day facility in Vatva, specializing in contract manufacturing for anti-tuberculosis, anti-malarial, and cardiovascular drugs. With ISO 7-compliant microbiology labs and walk-in stability chambers, Halewood supports global clients like Cadila and Ipca, maintaining GMP standards.

Our Mission

Deliver high-quality OSD and ORS products
Ensure GMP excellence and innovation
Foster a skilled, growth-oriented team

Attend the walk-in interview on May 17, 2025, or email careers@halewoodlabs.com. Join Halewood Laboratories in Vatva and advance global healthcare!