Leben Life Sciences Pvt. Ltd., a trusted name in pharmaceutical manufacturing for over 40 years, is seeking a skilled Quality Control Officer (HPLC) to join its EU-GMP approved facility in Akola, Maharashtra. This is an exciting opportunity for professionals passionate about ensuring high-quality pharmaceutical standards through expertise in High-Performance Liquid Chromatography (HPLC) and Good Laboratory Practices (GLP). If you’re looking to advance your career in pharmaceutical quality control, this role offers a dynamic work environment with a globally recognized leader in oral solid dosage (OSD) and semi-solids formulation. Apply now to be part of a company dedicated to excellence and innovation
Job Responsibilities
As a Quality Control Officer specializing in HPLC at Leben Life Sciences, you will play a vital role in maintaining the highest standards of pharmaceutical quality. Your key responsibilities include:
- Performing HPLC Analysis: Conduct precise analysis of raw materials, intermediates, and finished products using HPLC techniques to ensure compliance with quality standards.
- Ensuring GLP Compliance: Maintain Good Laboratory Practices in all quality control processes, adhering to EU-GMP and global regulatory guidelines.
- Method Validation and Troubleshooting: Execute analytical method validation, stability studies, and troubleshoot HPLC-related issues to ensure accurate results.
- Documentation and Reporting: Prepare detailed technical reports and document analytical results for internal audits and regulatory inspections.
- Equipment Calibration: Calibrate and maintain HPLC equipment to ensure optimal performance and system suitability.
- Collaboration: Work closely with cross-functional teams to uphold quality control excellence and support production goals.
Qualifications and Skills
To succeed in this role, candidates must meet the following requirements:
- Educational Background: M.Sc. in Chemistry, B.Pharm, or M.Pharm from a recognized university.
- Experience: 2-4 years of hands-on experience in HPLC analysis within the pharmaceutical industry, preferably in a quality control role.
- Technical Skills: Proficiency in HPLC techniques, method development, and validation. Familiarity with GLP, GMP, and analytical troubleshooting is essential.
- Soft Skills: Strong attention to detail, excellent problem-solving abilities, and effective communication skills for teamwork and reporting.
- Preferred Attributes: Knowledge of other analytical instruments (e.g., GC, UV-Vis) and experience with regulatory audits is a plus.
Benefits of Joining Leben Life Sciences
Working at Leben Life Sciences offers numerous advantages for career growth and personal development:
- Competitive Salary: Earn a market-competitive salary in the range of INR 3,00,000–5,00,000 per annum, based on experience and qualifications.
- Career Advancement: Access opportunities for professional growth in a leading pharmaceutical company with a global reputation.
- Collaborative Environment: Join a supportive team of experienced professionals in a state-of-the-art, EU-GMP approved facility.
- Work-Life Balance: Benefit from a workplace that values employee well-being, with a moderate work-life balance rating of 3.2/5 based on employee feedback.
- Industry Leadership: Contribute to a company with over four decades of excellence in pharmaceutical formulations.
How to Apply
Ready to take the next step in your pharmaceutical career? Interested candidates can send their updated resumes to career@lebenlifesciences.com with the subject line “Quality Control Officer – HPLC Application.” For inquiries, contact Leben Life Sciences at 7498035480. Applications are accepted until September 29, 2025. Don’t miss this opportunity to join a renowned pharmaceutical company in Akola, Maharashtra! Visit www.lebenlifesciences.com for more details about the company and its mission.
Frequently Asked Questions (FAQs)
Q1: What qualifications are required for the Quality Control Officer (HPLC) role at Leben Life Sciences?
A1: Candidates must hold an M.Sc. in Chemistry, B.Pharm, or M.Pharm with 2-4 years of experience in HPLC analysis within the pharmaceutical industry. Familiarity with GLP and GMP is essential.
Q2: What is the application process for this job?
A2: Send your updated resume to career@lebenlifesciences.com with the subject “Quality Control Officer – HPLC Application” or contact 7498035480 for more details. The application deadline is September 29, 2025.
