Officer QA Validation at HAB Pharmaceuticals and Research Ltd
HAB Pharmaceuticals and Research Ltd is currently hiring for the position of Officer QA Validation in the Quality Assurance department within the Pharmaceutical industry.
Roles & Responsibilities
HAB Pharmaceuticals & Research Ltd is inviting applications for the position of Officer QA at its pharmaceutical manufacturing facility in Dehradun, Uttarakhand. This full-time opportunity is suitable for B.Pharm professionals with 1 to 6 years of experience in pharmaceutical quality assurance operations. The selected candidate will play a critical role in maintaining quality systems, ensuring compliance with GMP guidelines, reviewing documentation, managing deviations, and supporting audit readiness activities. Candidates should possess a strong understanding of quality management systems, regulatory requirements, SOP compliance, and documentation control within a regulated pharmaceutical environment. This position offers an excellent opportunity to work with an established pharmaceutical organization committed to quality, compliance, and continuous improvement. Professionals seeking career growth in pharmaceutical quality assurance and regulatory compliance are encouraged to apply and become part of a dynamic quality-focused team.
Location
Dehradun, Uttarakhand, India
Employment Type
Full-time
Experience Required
1 to 6 years
Educational Qualification
B.Pharm
Key Responsibilities
- Review batch manufacturing and packaging records for compliance.
- Ensure implementation of GMP and quality assurance procedures.
- Manage deviations, investigations, and CAPA activities.
- Review SOPs, protocols, specifications, and validation documents.
- Support internal audits and regulatory inspection preparedness.
- Monitor documentation practices across manufacturing operations.
- Coordinate with production and QC teams on quality matters.
- Ensure timely closure of quality events and observations.
- Maintain quality records and compliance documentation.
- Participate in employee training on quality systems.
Required Skills & Competencies
- Knowledge of pharmaceutical quality assurance systems.
- Strong understanding of GMP and regulatory guidelines.
- Experience in deviation and CAPA management.
- Excellent documentation review skills.
- Ability to conduct compliance assessments.
- Strong analytical and problem-solving abilities.
- Good communication and coordination skills.
- Attention to detail and accuracy.
- Knowledge of audit and inspection requirements.
- Proficiency in quality documentation systems.
Why Join HAB Pharmaceuticals & Research Ltd?
HAB Pharmaceuticals & Research Ltd offers a professional work environment focused on quality, innovation, and compliance. Employees gain exposure to modern pharmaceutical manufacturing practices, regulatory systems, and continuous learning opportunities that support long-term career growth within the pharmaceutical industry.
How to Apply
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