HAB Pharmaceuticals and Research Ltd Walk-in Interview.HAB Pharmaceuticals and Research Ltd Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Department: Group Head Corporate Quality Assurance CQA, Pharma Formulations
- Experience: 12 – 15 years
- Qualification: B.Pharm or M.Pharm (mandatory).
- Salary: 15-20 Lacs P.A.
Important Details :
-
Work Location: Mumbai (All Areas)( Lower Parel )
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job Description: Greeting from HAB Pharmaceuticals and Research Ltd ….!!!
Role Overview
The Group Head Corporate QA (CQA) will lead the Quality Assurance function across all manufacturing plants of HAB Group. This role is responsible for establishing a unified Quality Management System (QMS), ensuring full compliance with current Indian and international quality standards, overseeing plant QA Heads, and driving continuous improvement and audit readiness across the organisation.
This is a senior leadership role based at the Head Office with strong influence across all factories, including OSD, Injectables, External Preparations, and upcoming facilities.
Key Responsibilities
A. Corporate QA Leadership
- Establish and lead the Corporate Quality Assurance function at the Head Office.
- Build, mentor, and expand the HO-based CQA team (audit, QMS, documentation, CAPA monitoring).
- Provide direction and oversight to all Plant QA Heads, ensuring alignment and standardisation.
B. Quality Management System (QMS)
- Develop, implement, and maintain a Group-wide QMS integrated across all sites.
- Standardise SOPs, MFR/BMRs, specifications, and documentation practices across units.
- Monitor and ensure effective control of deviations, change controls, OOS/OOT, CAPA closure, and QRM implementation.
- Track quality KPIs and drive improvements based on trend analysis.
C. Compliance & Regulatory Readiness
- Ensure consistent compliance with all Indian and international regulatory standards for pharma manufacturing.
- Maintain readiness for external audits from government agencies, certification bodies, and global customers.
- Oversee preparation for Revised Schedule M compliance across all plants.
- Guide teams on data integrity, documentation governance, and quality culture improvement.
D. Audits & Plant Oversight
- Conduct internal audits at all plants as per a predefined annual audit calendar.
- Ensure effective follow-up of audit findings until closure.
- Review and approve audit reports submitted by plant QA teams.
- Collaborate with Plant Heads and functional HODs to ensure timely corrective actions.
E. Continuous Improvement
- Identify systemic gaps across plants and lead cross-site improvement projects.
- Drive harmonisation of quality processes using risk-based approaches.
- Support technology adoption in QMS, including digital QA systems, e-logbooks, and document control systems.
- Promote a proactive quality culture across production, QC, QA, engineering, and support functions.
F. Vendor & External Requirements
- Oversee vendor qualification audits wherever needed (raw materials, packaging, service providers).
- Participate in customer audits, technical discussions, and product quality reviews.
Qualifications & Experience
- B.Pharm or M.Pharm (mandatory).
- 12–15 years of progressive QA experience in regulated pharmaceutical manufacturing.
- Strong exposure to:
- OSD manufacturing (primary)
- Injectables and external preparations (secondary)
- Demonstrated experience in QMS, internal audits, regulatory compliance, and team leadership.
Key Skills & Competencies
- Strong expertise in QA systems, documentation, and audit readiness.
- Ability to manage and guide multiple plant QA teams.
- Excellent understanding of pharmaceutical GMP, validation, data integrity, and risk management.
- High ownership, structured thinking, and problem-solving.
- Strong communication and ability to influence senior technical teams.
- Capability to drive group-wide cultural transformation in quality standards.
Leadership Attributes
- Quality-first mindset and uncompromising approach to compliance.
- Ability to work closely with directors and plant leadership teams.
- Structured project management and follow-up discipline.
- Balanced, practical approach with ability to implement on ground.
Walk In Interview Details
Date: 8th December – 10th December ,
Time: 9.30 AM – 5.30 PM
Venue:Hab Pharmaceuticals and Research Ltd., A301, Peninsula Business Park, Lower Parel, Mumbai 400013 (View on map)
