Job Description
HAB Pharmaceutical Research Limited is hiring talented professionals for the role of QC HPLC Officer at its pharmaceutical manufacturing facility located in Dehradun, Uttarakhand, India. This full-time opportunity is suitable for candidates with 0 to 5 years of experience in pharmaceutical quality control, HPLC analysis, analytical testing, laboratory operations, and GMP-regulated manufacturing environments. The selected candidate will perform HPLC analysis, maintain laboratory documentation, support quality control testing activities, coordinate with production and quality assurance departments, and ensure compliance with pharmaceutical quality standards and regulatory guidelines. Candidates having exposure to analytical instruments, laboratory practices, pharmaceutical testing methods, and quality systems will be preferred. This role provides valuable exposure to modern pharmaceutical analytical laboratories, quality management systems, regulatory environments, and advanced testing technologies focused on product quality, testing accuracy, operational efficiency, and compliance excellence within the pharmaceutical manufacturing industry.
Location
Dehradun, Uttarakhand, India
Employment Type
Full-time
Experience Required
0 to 5
Compensation & Benefits
Competitive salary package with analytical laboratory exposure, quality control learning opportunities, and long-term pharmaceutical career growth.
About HAB Pharmaceutical Research Limited
HAB Pharmaceutical Research Limited operates in the pharmaceutical industry specializing in healthcare manufacturing, analytical testing, quality systems, and regulated production environments.
Position Overview
The QC HPLC Officer will manage analytical testing activities, operate HPLC systems, and support pharmaceutical quality control operations.
Key Responsibilities
Perform HPLC analysis for pharmaceutical samples and materials.
Maintain laboratory documentation and testing records.
Support analytical testing and quality control activities.
Ensure compliance with GMP and laboratory standards.
Coordinate with production and quality assurance teams.
Monitor analytical instruments and laboratory equipment.
Participate in investigations and deviation handling processes.
Maintain sample management and analytical reporting systems.
Support audit preparation and regulatory inspections.
Assist in continuous quality improvement initiatives.
Required Skills & Competencies
Strong understanding of HPLC operations and analytical testing.
Knowledge of pharmaceutical quality control systems.
Documentation and reporting management abilities.
Communication and coordination skills.
Problem-solving and analytical thinking capabilities.
Awareness of GMP and pharmaceutical compliance standards.
Ability to manage laboratory activities efficiently.
Attention to analytical accuracy and product quality.
Operational planning and testing coordination expertise.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
BSc/MSc/BPharma/MPharma
About the Project & Industry
The pharmaceutical analytical testing industry depends on advanced laboratory technologies, quality systems, and compliance-driven operations to maintain product safety, healthcare standards, and manufacturing reliability.
Why Join HAB Pharmaceutical Research Limited?
HAB Pharmaceutical Research Limited offers opportunities to work in advanced pharmaceutical analytical environments with exposure to modern quality systems and laboratory technologies.
How to Apply
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