Halewood Laboratories Pvt. Ltd. is hiring pharmaceutical professionals for Corporate Quality Assurance (CQA) and Quality Management System (QMS) positions in Ahmedabad, Gujarat. Candidates with B.Pharm, M.Pharm, or relevant qualifications and experience in Oral Solid Dosage (OSD) formulations can apply for the respective positions.
Job Details
| Particulars | Details |
|---|---|
| Company | Halewood Laboratories Pvt. Ltd. |
| Industry | Pharmaceutical – OSD Formulations |
| Job Locations | Corporate Office, Ahmedabad; Unit 2, Bavla, Ahmedabad |
| Experience | 2–6 years, depending on the position |
| Qualification | B.Pharm/M.Pharm or relevant qualification |
| Application Email | careers@halewoodlabs.com |
| Contact Number |
Positions Available at Halewood Laboratories
1. Senior Officer/Executive/Senior Executive – Corporate Quality Assurance (CQA)
Location: Corporate Office, Ahmedabad
Experience: 3–6 years
Key Responsibilities
- Monitor compliance with cGMP and regulatory guidelines across manufacturing units.
- Review quality systems, SOPs, deviations, CAPA, change controls, and risk assessments.
- Coordinate internal and external audits and regulatory inspections.
- Review site-level quality documentation and monitor compliance status.
- Support the implementation and standardization of quality systems.
- Coordinate with plant QA/QC teams to improve quality processes and alignment.
Eligibility and Qualifications
- B.Pharm, M.Pharm, or a relevant qualification.
- 3–6 years of experience in Corporate Quality Assurance or Quality Assurance.
- Experience in Oral Solid Dosage (OSD) formulations is mandatory.
2. Senior Officer/Executive – Quality Management System (QMS)
Location: Unit 2, Bavla, Ahmedabad
Experience: 2–6 years
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Key Responsibilities
- Maintain and implement the Quality Management System in compliance with cGMP and regulatory requirements.
- Prepare, review, revise, and control SOPs and other quality documents.
- Manage deviations, CAPA, change controls, and non-conformances.
- Coordinate internal audits, customer audits, and inspections.
- Ensure timely closure of quality observations and track CAPA effectiveness.
- Maintain audit records, quality documentation, and reports.
- Coordinate with cross-functional departments to ensure compliance.
Eligibility and Qualifications
- B.Pharm, M.Pharm, or a relevant qualification.
- 2–6 years of experience in Quality Management Systems.
- Experience in Oral Solid Dosage (OSD) formulations is mandatory.
Required Skills and Expertise
Based on the listed responsibilities, relevant expertise includes:
- Pharmaceutical quality assurance and quality management systems.
- cGMP and regulatory compliance.
- SOP preparation, review, revision, and document control.
- Deviation management, CAPA, and change control.
- Risk assessment and non-conformance management.
- Internal and external audits and regulatory inspections.
- Quality documentation and coordination with QA/QC teams.
How to Apply for Halewood Laboratories Jobs
Interested and eligible candidates can share their CV with Halewood Laboratories Pvt. Ltd. using the following contact details:
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- Email: careers@halewoodlabs.com
